Giant freshwater prawn (Macrobrachium rosenbergii or GFP), is the most economically important freshwater crustacean species. However, as little is known about its genome, 454 pyrosequencing of cDNA was undertaken to characterise its transcriptome and identify genes important for growth.
Methodology and Principal Findings
A collection of 787,731 sequence reads (244.37 Mb) obtained from 454 pyrosequencing analysis of cDNA prepared from muscle, ovary and testis tissues taken from 18 adult prawns was assembled into 123,534 expressed sequence tags (ESTs). Of these, 46% of the 8,411 contigs and 19% of 115,123 singletons possessed high similarity to sequences in the GenBank non-redundant database, with most significant (E value < 1e–5) contig (80%) and singleton (84%) matches occurring with crustacean and insect sequences. KEGG analysis of the contig open reading frames identified putative members of several biological pathways potentially important for growth. The top InterProScan domains detected included RNA recognition motifs, serine/threonine-protein kinase-like domains, actin-like families, and zinc finger domains. Transcripts derived from genes such as actin, myosin heavy and light chain, tropomyosin and troponin with fundamental roles in muscle development and construction were abundant. Amongst the contigs, 834 single nucleotide polymorphisms, 1198 indels and 658 simple sequence repeats motifs were also identified.
The M. rosenbergii transcriptome data reported here should provide an invaluable resource for improving our understanding of this species' genome structure and biology. The data will also instruct future functional studies to manipulate or select for genes influencing growth that should find practical applications in aquaculture breeding programs.
Citation: Jung H, Lyons RE, Dinh H, Hurwood DA, McWilliam S, Mather PB (2011) Transcriptomics of a Giant Freshwater Prawn (Macrobrachium rosenbergii): De Novo Assembly, Annotation and Marker Discovery. PLoS ONE6(12): e27938. https://doi.org/10.1371/journal.pone.0027938
Editor: John Parkinson, Hospital for Sick Children, Canada
Received: September 15, 2011; Accepted: October 28, 2011; Published: December 8, 2011
Copyright: © 2011 Jung et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This research forms part of H. Jung's Ph.D project, and is supported by an International Postgraduate Research Scholarship (Australia) and a Queensland University of Technology Postgraduate Award (N7333978). Additional funding for this work was provided by Queensland University of Technology awarded to P. Mather (QUT VC NPSG award). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Of the 200 or so aquaculture species, decapod crustaceans including prawns, lobsters and crabs contribute substantially to the US$60 billion global industry . Amongst farmed crustaceans, the giant freshwater prawn (Macrobrachium rosenbergii) has increasingly become an aquaculture species of major commercial value, with revenue in Asia alone currently worth >US$1 billion annually –. Due to its high value, research is now focusing on improving the growth performance of farmed M. rosenbergii –. However, little is known about this species' basic biology and genome make-up so that they can be exploited to improve farm productivity of this species.
Genomics approaches are now being applied widely to elucidate genetic factors conferring economically significant traits and/or phenotypes and to manage genetic diversity in cultured crustacean species –. Whilst their application to cultured fish species has produced significant production gains, such gains are only beginning to be realized in penaeid species –, and no detailed genetic analyses have yet been reported for M. rosenbergii. Such basic information is essential to better understand a species' biology and to devise strategies to improve productivity in culture. DNA microsatellites – and mitochondrial DNA sequence comparisons  have been used to examine the phylogeography of M. rosenbergii ,  sampled from Asia and northern Australia and genes potentially associated with pathogen defence responses – and sexual maturation traits  have also been identified. However, more genome-wide or transcriptome-wide datasets have yet to be generated as a basis for functional genomics approaches – aimed at improving the aquaculture performance of this species.
Roche 454 Genome Sequencing FLX technology is particularly useful as a shotgun method for generating data broadly across novel genomes, and it is relatively cheap , ,  and exceptionally accurate –. Here it was used to characterize the transcriptome of M. rosenbergii using cDNA prepared from mRNA isolated from muscle, ovary and testis tissues. Expressed sequence tag (EST) sequences generated were assembled and annotated with putative functions where possible, and database searches were performed to identify candidate protein domains, genes and gene families potentially involved with growth. A variety of markers potentially useful for genomic population studies including simple sequence repeats (SSRs) located within coding regions and single nucleotide polymorphisms (SNPs) detected amongst deep coverage sequence regions reads are also reported.
Results and Discussion
Roche 454 GS-FLX sequencing and contig assembly
cDNA prepared to mRNA purified from muscle, ovary and testis tissues from M. rosenbergii were sequenced using the 454 GS-FLX platform. Sequences that passed basic quality standards were clustered and assembled de novo. In 454 sequencing run #1, a total of 121,214 EST sequences (total = 36.45 Mb) were assembled from mRNA isolated from either muscle or ovary tissue sampled from 6 adult females and preserved in ethanol prior to analysis. Average EST length was 295 nucleotides (nt). Assembly of high quality ESTs generated 1983 contigs averaging 673 nt in length. Due to technical issues with the first 454 GS-FLX run, the expected amount of data (200 Mb) was not retrieved. Therefore a second 454 sequencing run was conducted to increase genomic data, including the addition of testis-derived RNA. In 454 sequencing run #2, a total of 666,517 EST sequences were assembled from mRNA isolated from muscle and ovary from 9 adult females and 3 adult male testis tissues and preserved in RNAlater solution (Ambion) prior to analysis. Eyestalk-derived RNA was also extracted, but ultimately excluded from sequencing run #2 as quality control indicators suggested it contained PCR and proteinase inhibitors leading to failure of cDNA fragmentation, as detected in the bioanalyzer traces (samples were not fragmented). For the remaining three tissue types, the average EST length was 311 nt in 454 sequencing run #2. After removing adaptor sequences, the combined run #1 and #2 dataset contained 244.37 Mb of sequence comprising 787,731 reads averaging 310 nt in length, and the average coverage depth was 29.85 sequences per nucleotide position (Table 1). This average EST read length is longer and the sequencing coverage depth is substantially higher than has been reported in similar 454 sequencing analyses in non-model species including Glanville fritillary (197 nt at 2.3 x coverage; ), flooded or rose gum (245 nt; ) or shore pine (306 nt at 3.6 x coverage; ). As shown in Figure 1, assembly of high quality M. rosenbergii EST sequences generated 8,411 contigs varying in length from 40 nt to 7,531 nt (average 845 nt; total 212,142,540 nt), with 5,724 (68%) being >500 nt in length. The long individual read lengths combined with the 29.85-fold average coverage contributed to this high proportion of long contig sequences. Singletons ranged from 50 nt to 773 nt in length (average 279 nt, total 32,228,442 nt) (Figure 1). To our knowledge, this is the first comprehensive study of the transcriptome of M. rosenbergii.
The contig sequences are represented by solid bars and the singleton sequences by open bars.
Comparative analyses of ESTs
From BLASTx searches of M. rosenbergii EST coding sequences, 3,757 of the 8,411 (46%) contigs and 21,965 of the 115,123 (19%) singletons possessed significant similarity (E value <1e–5) with proteins in the GenBank non-redundant (nr) database (Table S1). As might be expected, coding sequences in the majority of contigs (80%) and singletons (84%) matched well to crustacean and other arthropod proteins (Figure 2) which are in agreement with previous prawn studies , . After redundant and ribosomal protein sequences were excluded, 2,448 contig and 10,627 singleton sequences were identified as putative genes based on BLASTx matches.
E value cut-off is 1e–5 and top 30 hit species distribution of gene annotations showing high homology to the Arthropoda (Insecta and Crustacea) phylum with known genome sequences. Only contig sequences were used. Bold text indicates non-Arthropod homology.
Species most represented in the BLASTx searches included some penaeid shrimps, crabs and freshwater and marine crayfish species including giant tiger shrimp (Penaeus monodon), green mud crab (Scylla paramamosain), fleshy shrimp (Fenneropenaeus chinensis), Kuruma shrimp (Marsupenaeus japonicas), white leg shrimp (Litopenaeus vannamei), red swamp crayfish (Procambarus clarkia), and American lobster (Homarus americanus). Similarities in EST coding sequences are indicative of close evolutionary relationship of M. rosenbergii with other crustaceans. Only a few contig (1.8%) or singleton (3.9%) coding sequences matched protein sequences reported for M. rosenbergii, and again this was expected due to the limited number of M. rosenbergii EST (2365) and protein sequences (373) currently available in the NCBI databases. The M. rosenbergii EST sequences generated here thus will vastly expand the number of genes identified in this species.
More putative gene ESTs were detected in mRNA isolated from ovary tissue than from muscle or testis tissue (Figure 3). Only around 4% of the 3,757 contigs and 14% of the 21,965 singletons significantly matched either predicted or hypothetical genes (E value <1e–5) due to the limited genomic information available for prawn species in the public database (Table S1). A significant number of M. rosenbergii ESTs did not possess coding sequences matching any sequences in the GenBank nr database which is not surprising for prawn EST studies , . Whilst most of these likely represent ESTs spanning only untranslated mRNA regions, chimeric EST sequences derived from assembly errors or ESTs containing non-conserved protein regions, as reported in other transcriptome analyses –, it is also possible that some may constitute novel genes unique to this species.
Putative sequence descriptions were counted using BLASTx results (E-value <1e–5) after excluding ribosomal proteins and redundant ones. Bold numbers indicate contigs and numbers in italics indicate singletons.
Amongst ESTs derived from muscle tissue, coding sequences with homology to arginine kinase, ATP synthase, eukaryotic translation initiation factor, myosin heavy and light chain, sarcoplasmic calcium-binding protein, tropomyosin, and troponin were most abundant. Amongst ESTs derived from ovary tissue, coding sequences with homology to aldehyde dehydrogenase, ATP binding, cd63 antigen, cell division cycle, Chk1 checkpoint-like protein, e3 ubiquitin, eukaryotic translation initiation factor, ovary development-related protein, serine threonine-protein kinase, transmembrane protein, and WD repeat-containing protein were most abundant. Amongst ESTs derived from testis tissue, coding sequences with homology to eukaryotic translation initiation factor, kazal-type proteinase inhibitor, male reproductive-related protein, serine proteinase inhibitor, and viral A-type inclusion protein were most abundant. ESTs detected commonly across the 3 tissues included actins, elongation factors, eukaryotic translation initiation factor, heat shock protein, NADH dehydrogenase, reverse transcriptase, RNA-binding protein, senescence-associated protein, tubulin, ubiquitin and zinc finger protein (Figure 3, Table S1). Although this work was mainly focused on finding putative genes related with muscle development and growth, several putative functional transcripts identified here will lay the foundation for future studies aimed at investigating the role of sex determination, reproduction-related and xenobiotic genes which have been studied successfully in other species , , . These findings could be the best source for deciphering the putative function of novel genes in each tissue but further studies need to be conducted to understand the molecular functions of specific reported genes.
Gene Ontology assignments
Gene Ontology (GO) terms could be assigned to 8411 M. rosenbergii contigs based on BLAST matches to proteins with known functions (Figure 4, Table S2). EST coding sequences were assigned to cellular components (4,550 sequences, Figure 4A), molecular function (6,055 sequences, Figure 4B) and biological processes (8,806 sequences, Figure 4C). Amongst ESTs assigned molecular functions, many were assigned binding (45.9%) or catalytic functions (32.3%), predominantly actin and zinc ion proteins (Table S2). Recent studies of crustaceans have highlighted the importance of actin in constructing muscle tissues and that it shows variable expression in different muscle types –. The cellular component assignments showed many EST coding sequences to likely possess cell (22.8%) and cell part (22.5%) functions, whilst those assigned biological functions were mostly predicted to be involved in cellular (17.6%) or metabolic processes (16.5%) including proteolysis, carbohydrate metabolism or oxidation-reductive functions. Analyses of the transcriptomes of other crustaceans have identified ESTs possessing similar arrays of potential metabolic functions , , , .
Many of the coding sequences present in the M. rosenbergii EST contig dataset were identified to occur in KEGG pathways; metabolic pathways (n = 320), biosynthesis of secondary metabolites (n = 135), oxidative phosphorylation (n = 66), biosynthesis of phenylpropanoids (n = 59), and biosynthesis of alkaloids derived from histidine and purine (n = 51) (Table S3). Metabolic pathways, implicated in the kinetic impairment of muscle glutamine homeostasis in adult and old glucocorticoid-treated rats , showed the highest number of transcripts here. A skeletal muscle structure in rat intrauterine growth restriction indicated that changes in metabolic pathways were involved in obesity . A total of 66 transcripts were involved in oxidative phosphorylation. The integrity of the inner membrane and the associated complexes is essential to oxidative phosphorylation to generate ATP to supply readily-available free energy for the body . However, malfunction of oxidative phosphorylation could accentuate ATP depletion with the basic energy conservation system due to anoxic conditions in the tissues which could lead to metabolic failure .
Interestingly, we recovered a high number of transcripts that were mapped to the phenylpropanoids biosynthesis pathway (59). Phenylpropanoids not only play an important role in contributing to all aspects of plant responses towards biotic and abiotic stimuli  but also have a potential dietary importance from plant derived compounds . A total of 51 transcripts also were predicted to the alkaloid biosynthesis pathway from histidine and purine in the M. rosenbergii EST contig dataset. Alkaloids, regarded as basic plant derived metabolites, are important components of plant defence, growth and development systems , . In a study of sponges and ascidians, an abundance of alkaloids was reported that displayed biological activities such as metabolites . Considering the omnivorous dietary habit of M. rosenbergii, finding these pathways was not surprising. Although not all of the major genes reported in putative KEGG pathways were found in the current study, this information provides insight into the specific responses and functions involved in molecular processes in M. rosenbergii metabolism and muscle contraction against biotic and abiotic stimuli.
InterProScan searches identified 19,036 protein domains among the 8,411 M. rosenbergii contigs (Table S4). Consistent with similar analyses in insects and other crustaceans , , , domains that dominated occur in RNA-binding proteins, protein kinases and transcription factors (zinc finger domains) that are essential for cellular processing functions including signal transduction and transcription regulation, regulation of RNA stability and translation control (RNA recognition motifs), innate immunity, cell division, proliferation, apoptosis and cell differentiation , .
The most common DNA-binding motifs present in eukaryotic and prokaryotic transcription factors  were prevalent in the M. rosenbergii sequences, with 179 C2H2-type and 102 C2H2-like zinc finger (Znf) domains identified. Transcription factors usually contain several Znf domains capable of making multiple contacts with DNA , and can also bind to RNA and protein targets . A total of 112 nucleotide-binding α-β plait domains found in RNA-binding domains from various ribonucleoproteins or in viral DNA-binding domains ,  were predicted to exist among the M. rosenbergii EST coding sequences. In addition, 108 Armadillo-type fold and 84 Armadillo-like helical domains which form structural domains consisting of a multi-helical fold comprised of 2 curved layers of α-helices , were predicted (Table 2).
Among M. rosenbergii EST coding sequences, 104 domains containing WD40/YVTN repeat-like sequences, 90 domains containing WD40-repeat sequences and 88 domains containing WD40 repeat-like sequences were predicted (Table 2). These domains are involved in a variety of functions ranging from signal transduction and transcription regulation to cell cycle control and apoptosis , . A total of 86 Ran GTPase families which are involved in regulating GTP hydrolases , contain GTP-binding domains  and regulate receptor-mediated transport between the nucleus and the cytoplasm ,  were also predicted, as were 84 immunoglobulin (Ig)-like fold domains (Table 2). Ig-like fold domains are involved in a variety of functions including cell-cell recognition, cell-surface receptors, muscle structure and the immune system , and are often involved with protein-protein interactions mediated by their β-sheets as in other Ig-like domains , . Other domains identified abundantly included Serpin (serine proteinase inhibitor) domains (n = 79) and NAD(P)-binding domains (n = 72) (Table 2). Interestingly, few PAZ (n = 3) or PIWI (n = 8) domains believed to be important components of the dsRNA-induced silencing complex were identified. The relative absence of ESTs with such domains is perplexing based on the detection of genes encoding Dicer and Argonaut type proteins in penaeid shrimp – and the clear demonstration of effective RNAi-mediated knockdown of gene expression in shrimp . Similar transcriptome analyses of other tissues including haemocytes from the lymphoid organs for example that are primary mediators of pathogen defence responses , ,  might be useful for indentifying if expression of ESTs encoding putative RNAi-related domains are more cell specific than domains required broadly for cell functioning. Although an original aim of this study was to identify candidate genes, gene families or gene domains potentially involved with growth phenotypes and/or other production traits important for M. rosenbergii aquaculture, none were differentiated from cell function or pathogen defence type activities. The identification of such ESTs has been confounded in most studies of shrimp to date focussing on the identification and characterisation of pathogen defence-related genes , , . Thus genes mediating growth performance and potentially of value in selective breeding programs await discovery.
Putative genes affecting muscle development and/or function
The M. rosenbergii EST sequence database was mined for coding sequences with domains involved potentially with muscle development and function (Table 3). Despite recent advances in sequencing technologies, few genes with such functions have been characterised from any crustaceans, and only 2365 ESTs assigned to M. rosenbergii and 5536 ESTs assigned to Macrobrachium were available in NCBI databases before this study. However, the 123,534 ESTs from the M. rosenbergii individuals selected from high and low growth performance cohorts should contain genes potentially expressed differentially and with functional characteristics suggestive of roles in muscle mass accumulation and other growth-related functions.
In the current study, both actin and myosin proteins including tropomyosin and troponin showed a high number of transcripts. It has been reported that actins are expressed in abundance as they are critical to formation of muscle filaments , . Different actin isoforms have been identified in various crustaceans , and are likely to be involved in playing important roles in cytoskeletal structure, cell division and mobility, and muscle contraction –. The large super-family of myosin proteins interact with actin filaments by hydrolysing adenosine triphosphate that combine to form thick muscle filaments . Myosin heavy chain (MHC) isoforms differ in their shortening velocity compared with other isoforms due to the enhanced ability of the myosin head to hydrolyse ATP . Multiple MHC isoforms are expressed ubiquitously in all eukaryotic cells and they are the most abundant contractile protein present in skeletal muscle , . If growth rates of M. rosenbergii are dictated primarily by the efficiency at which feed is converted into muscle mass, it is likely that myosin gene expression levels could provide a good molecular marker of individual growth potential, as found in the Atlantic pink shrimp Farfantepenaeus paulensis . In studies of other crustaceans, high expression levels of genes encoding fast and slow myosin isoforms have been found to be accompanied by elevated expression of other genes encoding for example, actin, myofibrillar protein, tropomyosin, troponin I, and troponin T –. According to Perry et al. , differences in expression levels of myofibrillar protein isoforms correlate well with individual body size in crabs, with changes in expression spanning several orders of magnitude occurring at different life stages. Tropomyosins comprise a family of closely related proteins present both in muscle and non-muscle cells . In striated muscle, tropomyosin mediates interactions between the troponin complex and actin to mediate muscle contraction . A high number of actin and myosin protein transcripts observed here may regulate muscle development and function in M. rosenbergii. However, further studies are needed to confirm these observations.
High occurrence of calponin and transgelin was also observed in the transcriptome of M. rosenbergii. Calponin is a smooth muscle-specific protein capable of binding actin, tropomyosin and calmodulin and is also involved in mediating muscle contraction  as its interaction with actin inhibits actomyosin Mg-ATPase activity. In previous studies of invertebrates and vertebrates, caldesmon and calponin were shown to interact with actin, tropomyosin, and Ca2+-calmodulin , , . In addition, transgelin is a calponin which is expressed exclusively in smooth muscle-containing tissues in adult animals and is one of the earliest markers of differentiated smooth muscle cells , .
The current study reports a number of putative genes, transcription factors, and early regulators that are potentially involved in muscle development and function in M. rosenbergii. Further studies need to be performed, however, to learn the molecular functions of these reported genes which were observed to be expressed more abundantly in adult female and male prawns compared with earlier developmental stages or slow growth performance individuals.
Genes of interest related to growth
The transcriptome of M. rosenbergii was examined primarily to identify genes associated functionally with individual growth. For this reason, an EST dataset was compiled from tissues of individuals from high and low growth performance families (Table 3). Amongst these, a putative cyclophilin was identified. Although cyclophilins possess diverse functions and have been linked to innate immunity ,  and testicular development , expression levels of cyclophilin-like proteins have also been found to be highly correlated with body-weight in the shrimp P. monodon .
Intracellular fatty acid-binding proteins (FABPs), identified in the current transcriptomic study, are members of a lipid-binding protein super-family that occur in both invertebrates and vertebrates, and together with acyl-CoA-binding protein (ACBP) are involved in lipid metabolism . Few FABPs have been identified in invertebrates , , and their physiological roles remain largely unknown. However, in the locust Schistocerca gregaria, FABP expression has been reported to be strictly adult specific and is controlled by fatty acids in adult muscle . Locust flight muscle employs fatty acids exclusively as the energy source for sustained flight and it is likely that FABP is involved in intracellular fatty acid transport .
In the current study, we found high occurrence of LIM domain proteins, which play important biological roles in cytoskeleton organisation, cell fate determination and organ development . Previously, one LIM domain gene (ISL1) has been identified as a positional candidate for obesity and for controlling leptin levels, and is suggested to be involved in body weight regulation and glucose homeostasis . In a study of the red crab Gecarcoidea natalis, two genes encoding LIM proteins, a paxillin-like transcript (pax) and a muscle LIM protein (mlp), were up-regulated in muscle of crabs in the wet season . These proteins could play a fundamental role in muscle development and reconstruction, and their comparative up-regulation is consistent with a remodelling of leg muscle needed for migration during the wet season .
Physiologically, O-methyltransferase (OMT) plays an important regulatory role in plant and animal growth, development, reproduction and immune response , . OMT transcripts observed in the current study could represent a potential candidate gene for developing novel traits in prawns. Methyl farnesoate (MF), the sesquiterpenoid precursor of insect juvenile hormone III (JH III), is produced and released by mandibular organs in decapod crustaceans –. The physiological function of MF, however, is not well understood in crustaceans, but by analogy with established functions of JH III in insects, MF has been suggested to play an important role in regulation of growth and reproduction in crustaceans , . In some crustaceans, circulating titer and biosynthesis of MF appear to be correlated positively with maturation of the ovary , . MF has also been suggested to play a role in delaying onset of molting in larval crustaceans , . This evidence implicates MF in both crustacean growth and reproduction. Farnesoic acid O-methyltransferase (FAMeT; also known as S-adenosyl-methionine:farnesoic acid O-methyltransferase) is the enzyme that catalyses the final step in the MF biosynthetic pathway in crustaceans , . Studies of crustacean FAMeT indicate that it may directly or indirectly (through MF) modulate reproduction and growth in crustaceans – by interacting with eyestalk neuropeptides as a consequence of its presence in neurosecretory cells in the X-organ-sinus gland. It is also believed that MF is the crustacean homolog for insect juvenile hormone, a molecule that may also regulate growth and reproduction in crustaceans . If growth rates of M. rosenbergii are dictated primarily by the efficiency at which feed is converted into muscle mass, it is likely that FABP, LIM domain and FAMeT gene expression levels could provide candidate molecular markers of individual growth potential.
Another interesting finding in the current study is the expression of profilin, a small actin-binding protein found in eukaryotic cells that is critical for cytoskeletal dynamics , . Profilins are potent regulators of actin filament dynamics and promote exchange of ADP to ATP on actin and by affinity to profilin–actin complexes for actin filament ends . Profilins have diverse roles in cellular processes, including membrane trafficking, small-GTPase signalling and nuclear activities, neurological diseases, and tumor formation –. Genetic studies have shown the importance of profilins for cell proliferation and differentiation. Profilin gene disruption leads to grossly impaired growth, motility and cytokinesis, and embryonic lethality in multicellular organisms, for example in insects and mice –.
The current study identified a number of putative genes that are potentially involved with growth in M. rosenbergii. However, further studies are needed to understand the molecular functions of these putative genes with growth performance and development in M. rosenbergii.
Putative Molecular Markers
SNPs in M. rosenbergii EST contigs were identified from alignments of multiple sequences used for contig assembly. Of the 834 SNPs detected, 555 were putative transitions (Ts) and 279 were putative transversions (Tv), giving a mean Ts : Tv ratio of 1.99 : 1.00 across the transcriptome (Figure 5, Table S5). The SNP types A ↔ G and C ↔ T were most common and SNP densities varied among genes, possibly due in part, to the effects of strong historical selection and the relative functional importance of individual genes. The Ts : Tv ratio can help identify genes affected by selection . Although alignments also identified a total of 1198 indels across the transcriptome (Figure 5, Table S5), this must be treated with caution because of technical problems associated with 454 pyrosequencing , . Moreover, a total 658 simple sequence repeats (SSRs) or microsatellites comprising 61.85% dinucleotide repeats, 35.87% trinucleotide repeats and 2.28% tetra/penta/hexa-nucleotide repeats were detected (Figure 6, Table S6) in the contigs as well as singletons.
Both contig and singleton sequences are used to predict the SSR loci.
PCR primers could be designed for almost all predicted polymorphic SSRs (Table S6) but these have yet to be validated as markers useful for examining M. rosenbergii adaptation and ecology as has been done with other non-model species –. In addition, SNPs and SSRs detected here are likely to be highly transferable to other closely related species as has been found for other crustacean species –. It is envisaged that the potential markers identified here within the ESTs will provide an invaluable resource for studying the evolution and molecular ecology of Macrobrachium species and for genome mapping and quantitative trait loci (QTL) analysis. However, many of the putative M. rosenbergii SNPs identified could simply represent allelic variants and future studies are planned to validate which are real. As ESTs were generated from 3 different tissue types, differential expression of different tissue-specific alleles is possible. However, this is rare as it requires somatic mutation or chimerisms between tissues.
Here we report the first comprehensive EST dataset covering the transcriptome of the giant freshwater prawn M. rosenbergii, a non-model prawn species for which little molecular knowledge currently exists. The 123,534 putative ESTs (115,123 singletons and 8,411 contigs) identified and assembled will enable gene discovery in M. rosenbergii, assist in evolutionary studies and with the significant number of putative growth-related genes identified should facilitate genomics approaches to improving the growth performance of domesticated GFP stocks used for aquaculture. In addition, the large number of SNPs and SSRs detected provide targets for identifying polymorphisms across M. rosenbergii populations useful for parentage assignment and for managing inbreeding in cultured populations. Moreover, the EST sequences reported should prove invaluable for gene mining and annotation and phylogenetic analyses as well as provide a resource that can be exploited as molecular markers and in gene expression studies in this commercially important aquaculture species.
M. rosenbergii with variable growth phenotypes were sampled from cohorts that were reared in a GFP stock improvement program in Vietnam . Muscle and ovary tissue was sampled from adult females from high and low growth performance families and tissues preserved in 95% ethanol (454 sequencing run #1). Muscle was not sampled from males as their growth performance is confounded by social factors . Muscle and ovary tissue from adult females and testis and eye-stalk tissue from adult males preserved in RNAlater (Ambion) were also analysed (454 sequencing run #2).
In 454 sequencing run #1, TRIzol® reagent (Invitrogen)  was used to extract total RNA from either muscle tissue or ovary tissue pooled from the three heaviest females from the high growth performance cohort and from the three lightest females from the low growth performance cohort. In 454 sequencing run #2, total RNA was extracted similarly from muscle/ovary (female) and testis/eye-stalk (male) from groups of three prawns in the same growth categories as used in 454 sequencing run #1. Total RNA was purified further using a RNA Easy Kit (QIAGEN). RNA yields and quality were checked using both a Bioanalyzer nanochip (Agilent) and a Nanodrop spectrophotometer (Thermo). Equal amounts of total RNA purified from each tissue type were pooled and mRNA was isolated using the MicroPoly(A) Purist™ Kit (Ambion) according to the manufacturer's protocol.
Library construction and 454 pyrosequencing
mRNA purified from pooled muscle, ovary, testis and eye-stalk total RNA from males and females of high and low growth performance were sent to the Australian Genome Research Facility (AGRF), Brisbane, Australia, for cDNA synthesis using a cDNA Rapid Library Preparation Kit (Roche) and subjected to 454 GS-FLX sequence analysis. Due to issues with poor RNA and cDNA quality and low yields from eyestalk tissue, this tissue was excluded from the cDNA library. The cDNA library sequenced thus comprised a pool of cDNAs prepared from muscle tissue from the three heaviest females, ovary tissue from the three heaviest and three lightest females and testis tissue from the three heaviest males. Each cDNA was normalized prior to pooling to reduce sequence coverage of high copy number mRNAs and samples tagged for downstream identification. cDNA yields were quantified using a Quant-iT RiboGreen fluorometer (Invitrogen) and average lengths were determined by analysis of an aliquot (1 µl) on the Bioanalyzer (Agilent) using a LapChip 7500. Oligonucleotide adapters A and B (Roche) were ligated to cDNA 5′ and 3′ ends and cDNA was amplified by PCR using the same primers and a proof reading polymerase. Emulsion PCR (emPCR) set up, breaking, enrichment and pico-titer plate (PTP) loading steps were performed according to Roche protocols . Each of the two sequencing runs employed half of a PTP and was sequenced twice using Roche 454 GS FLX chemistry (Roche) according to the manufacturer's protocol.
Sequence cleaning and assembly
All sequence reads taken directly from the 454 GS-FLX sequencer were run through the sff file program (Roche) to remove sequencing adapters A and B, poor sequence data and barcodes. Contigs and singletons were renamed in a format ‘A (M, O, T)_000001’ where prefix ‘A’ was used for all assembled contigs derived from M, O, T cDNA libraries, with M (Muscle), O (Ovary), and T (Testis) standing for an individual library and assembly, and 000001 standing for the first arbitrary contig assignment number. In the case of singletons, the same prefix codes (A, M, O, T) for cDNA library origin(s) were added in front of each read name (e.g. A_G1OH9PT01AF0I7). Sequences containing homopolymers of a single nucleotide comprising >60% of the read and that were >100 nucleotides in length were discarded. Trimmed sequences were assembled de novo using the default parameters of Newbler 2.5.3 (Roche). Each dataset of mRNA sequences from muscle, ovary and testis tissue was considered separately as being representative of the transcriptome of that tissue type at the time of sampling. On the assumption that some transcripts would be replicated across tissue-type datasets, these were merged in the combined dataset. After initial quality filtering, AGRF provided assembled contig and singleton datasets for analysis. All M. rosenbergii EST sequences obtained were submitted to NCBI Sequence Read Archive under Accession no. SRP007672.
Annotation of mRNAs
BLASTx searches  of the GenBank non-redundant (nr) database hosted by the National Center for Biotechnology Information (NCBI) (http://www.ncbi.nlm.nih.gov/) were performed on all contigs and singletons to identify putative mRNA functions (E-value threshold <1e–5) as well as new ESTs. Numbers of ESTs that were either unique or shared among the libraries were visualized using a 3-way Venn diagram constructed using Venny . Total EST numbers in the Venn diagram quadrants excluding abundant ESTs for ribosomal proteins counted redundant ESTs only once. The Blast2GO software suite ,  was used to predict functions of individual ESTs, assign Gene Ontology terms , , and to predict metabolic pathways using Kyoto Encyclopaedia of Genes and Genome (KEGG) , . To identify protein domains, all translated sequences were interrogated against the InterPro databases (http://www.ebi.ac.uk/Tools/pfa/iprscan/) using the InterProScan tool . The numbers of contigs annotated with each GO term for each library were quantified using WEGO .
Identification of EST-SSR motifs and EST-SNPs
All EST sequences were searched for SSR motifs using the QDD program . Default settings were employed to detect perfect di-, tri-, tetra-, penta-, and hexa-nucleotide motifs (including compound motifs). To be assigned, dinucleotide SSRs required a minimum of 6 repeats, and all other SSR types a minimum of 5 repeats. The maximum interruption between 2 neighbouring SSRs to consider it being a compound SSR was set at 100 nucleotides. Perl script modules linked to the primer modelling software Primer3  were used to design PCR primers flanking for each unique SSR region identified.
Multiple nucleotide sequence alignments of contigs identified among the EST libraries derived from individual M. rosenbergii with divergent growth phenotypes were undertaken to identify putative SNPs. Alignments employed methods developed previously for plants and other species of agricultural importance , ,  and included assessments of raw data alignments used in the initial assembly of contigs. Since no reference sequences were available, SNPs were identified as superimposed nucleotide peaks where 2 or more reads contained polymorphisms at the variant allele. SNPs were identified using default parameters in gsMapper (Roche) to align contigs from the individual and merged tissue type and prawn phenotype datasets and SNPs were predicted with high confidence when (i) the difference existed in at least three non-duplicated reads, (ii) the difference occurred in both the forward and reverse sequence reads unless present in at least seven same direction reads with quality scores over 20 (or 30 if the difference involves a 5-mer or more) and (iii) the difference comprised a single-base overcall or undercall forming a consensus differing from the each contig reference. Indels were segregated into simple types containing an insertion or deletion of at least one nucleotide compared with the reference sequence or complex types also containing nucleotides substitutions.
For the merged EST dataset, loose or strict criteria to maximize the discovery of rare alleles or to minimize the possibility of false-positive identifications were not considered , . In addition, only an overall transition vs transversion (Ts/Tv) ratio was calculated across the dataset.
Summary of BLASTx results for contigs and singletons of M . rosenbergii .
Gene Ontology of M . rosenbergii contig sequences.
KEGG summary of M . rosenbergii contig sequences.
InterProScan domain search of M . rosenbergii contig sequences.
Putative SNPs and Indels in M . rosenbergii contig sequences.
The authors would like to acknowledge the help provided by the Australian Genome Research Facility (Matthew Tinning, Tim Bruxner, Rachel Kliese, and Adam Skarshewski) in regard to pyrosequencing and initial analysis of the raw sequence data. The authors thank Markus Dwyer for assisting with computer service. We also thank Leanne Dierens and Barney Hines for assisting with RNA isolations. We gratefully acknowledge Jeffrey Cowley, Nick Hudson, Woo-Jin Kim, Peter Prentis and two anonymous reviewers' contributions for providing constructive comments on the manuscript.
Conceived and designed the experiments: HJ REL DAH PBM. Performed the experiments: HJ REL. Analyzed the data: HJ SM. Contributed reagents/materials/analysis tools: HJ REL PBM. Wrote the paper: HJ REL DAH PBM. Established breeding line: HD. Collected samples: HD.
- 1. FAO (2009) Fisheries Statistical Database, Global Aquaculture Production (Fisheries Global Information System, online query). FAO2009Fisheries Statistical Database, Global Aquaculture Production (Fisheries Global Information System, online query)
- 2. Thanh NM, Nguyen NH, Ponzoni RW, Vu NT, Barnes AC, et al. (2010) Estimates of strain additive and non-additive genetic effects for growth traits in a diallel cross of three strains of giant freshwater prawn (Macrobrachium rosenbergii) in Vietnam. Aquaculture 299: 30–36.NM ThanhNH NguyenRW PonzoniNT VuAC Barnes2010Estimates of strain additive and non-additive genetic effects for growth traits in a diallel cross of three strains of giant freshwater prawn (Macrobrachium rosenbergii) in Vietnam.Aquaculture2993036
- 3. Thanh NM, Barnes AC, Mather PB, Yutao L, Lyons RE (2010) Single nucleotide polymorphisms in the actin and crustacean hyperglycemic hormone genes and their correlation with individual growth performance in giant freshwater prawn Macrobrachium rosenbergii. Aquaculture 301: 7–15.NM ThanhAC BarnesPB MatherL. YutaoRE Lyons2010Single nucleotide polymorphisms in the actin and crustacean hyperglycemic hormone genes and their correlation with individual growth performance in giant freshwater prawn Macrobrachium rosenbergii.Aquaculture301715
- 4. Schwantes VS, Diana JS, Yi Y (2009) Social, economic, and production characteristics of giant freshwater prawn Macrobrachium rosenbergii culture in Thailand. Aquaculture 287: 120–127.VS SchwantesJS DianaY. Yi2009Social, economic, and production characteristics of giant freshwater prawn Macrobrachium rosenbergii culture in Thailand.Aquaculture287120127
- 5. Nhan DT, Wille M, Hung LT, Sorgeloos P (2009) Comparison of reproductive performance and offspring quality of giant freshwater prawn (Macrobrachium rosenbergii) broodstock from different regions. Aquaculture 298: 36–42.DT NhanM. WilleLT HungP. Sorgeloos2009Comparison of reproductive performance and offspring quality of giant freshwater prawn (Macrobrachium rosenbergii) broodstock from different regions.Aquaculture2983642
- 6. Thanh NM, Ponzoni RW, Nguyen NH, Vu NT, Barnes A, et al. (2009) Evaluation of growth performance in a diallel cross of three strains of giant freshwater prawn (Macrobrachium rosenbergii) in Vietnam. Aquaculture 287: 75–83.NM ThanhRW PonzoniNH NguyenNT VuA. Barnes2009Evaluation of growth performance in a diallel cross of three strains of giant freshwater prawn (Macrobrachium rosenbergii) in Vietnam.Aquaculture2877583
- 7. Staelens J, Rombaut D, Vercauteren I, Argue B, Benzie J, et al. (2008) High-density linkage maps and sex-linked markers for the black tiger shrimp (Penaeus monodon). Genetics 179: 917–925.J. StaelensD. RombautI. VercauterenB. ArgueJ. Benzie2008High-density linkage maps and sex-linked markers for the black tiger shrimp (Penaeus monodon).Genetics179917925
- 8. Du ZQ, Ciobanu DC, Onteru SK, Gorbach D, Mileham AJ, et al. (2010) A gene-based SNP linkage map for pacific white shrimp, Litopenaeus vannamei. Anim Genet 41: 286–294.ZQ DuDC CiobanuSK OnteruD. GorbachAJ Mileham2010A gene-based SNP linkage map for pacific white shrimp, Litopenaeus vannamei.Anim Genet41286294
- 9. Robalino J, Carnegie RB, O'Leary N, Ouvry-Patat SA, de la Vega E, et al. (2009) Contributions of functional genomics and proteomics to the study of immune responses in the Pacific white leg shrimp Litopenaeus vannamei. Vet Immunol Immunopathol 128: 110–118.J. RobalinoRB CarnegieN. O'LearySA Ouvry-PatatE. de la Vega2009Contributions of functional genomics and proteomics to the study of immune responses in the Pacific white leg shrimp Litopenaeus vannamei.Vet Immunol Immunopathol128110118
- 10. Wu P, Qi D, Chen L, Zhang H, Zhang X, et al. (2009) Gene discovery from an ovary cDNA library of oriental river prawn Macrobrachium nipponense by ESTs annotation. Comp Biochem Physiol Part D Genomics Proteomics 4: 111–120.P. WuD. QiL. ChenH. ZhangX. Zhang2009Gene discovery from an ovary cDNA library of oriental river prawn Macrobrachium nipponense by ESTs annotation.Comp Biochem Physiol Part D Genomics Proteomics4111120
- 11. Tassanakajon A, Klinbunga S, Paunglarp N, Rimphanitchayakit V, Udomkit A, et al. (2006) Penaeus monodon gene discovery project: The generation of an EST collection and establishment of a database. Gene 384: 104–112.A. TassanakajonS. KlinbungaN. PaunglarpV. RimphanitchayakitA. Udomkit2006Penaeus monodon gene discovery project: The generation of an EST collection and establishment of a database.Gene384104112
- 12. Lyons RE, Dierens LM, Tan SH, Preston NP, Li Y (2007) Characterization of AFLP markers associated with growth in the Kuruma prawn, Marsupenaeus japonicus, and identification of a candidate gene. Mar Biotechnol 9: 712–721.RE LyonsLM DierensSH TanNP PrestonY. Li2007Characterization of AFLP markers associated with growth in the Kuruma prawn, Marsupenaeus japonicus, and identification of a candidate gene.Mar Biotechnol9712721
- 13. Hamasaki K, Kitada S (2008) Potential of stock enhancement for decapods crustaceans. Rev Fisheries Sci 16: 164–174.K. HamasakiS. Kitada2008Potential of stock enhancement for decapods crustaceans.Rev Fisheries Sci16164174
- 14. Leekitcharoenphon P, Taweemuang U, Palittapongarnpim P, Kotewong R, Supasiri T, et al. (2010) Predicted sub-populations in a marine shrimp proteome as revealed by combined EST and cDNA data from multiple Penaeus species. BMC Res Notes 3: 295.P. LeekitcharoenphonU. TaweemuangP. PalittapongarnpimR. KotewongT. Supasiri2010Predicted sub-populations in a marine shrimp proteome as revealed by combined EST and cDNA data from multiple Penaeus species.BMC Res Notes3295
- 15. Leu J, Chen S, Wang Y, Chen Y, Su S, et al. (2011) A review of the major Penaeid shrimp EST studies and the construction of a shrimp transcriptome database based on the ESTs from four Penaeid shrimp. Mar Biotechnol 13: 608–621.J. LeuS. ChenY. WangY. ChenS. Su2011A review of the major Penaeid shrimp EST studies and the construction of a shrimp transcriptome database based on the ESTs from four Penaeid shrimp.Mar Biotechnol13608621
- 16. Chand V, de Bruyn M, Mather PM (2005) Microsatellite loci in the eastern form of the giant freshwater prawn (Marcrobrachium rosenbergii). Mol Ecol Notes 5: 308–310.V. ChandM. de BruynPM Mather2005Microsatellite loci in the eastern form of the giant freshwater prawn (Marcrobrachium rosenbergii).Mol Ecol Notes5308310
- 17. Divu D, Khushiramani R, Malathi S, Karunasagar I, Karunasagar I (2008) Isolation, characterization and evaluation of microsatellite DNA markers in the giant freshwater prawn, Marcrobrachium rosenbergii, from South India. Aquaculture 284: 481–284.D. DivuR. KhushiramaniS. MalathiI. KarunasagarI. Karunasagar2008Isolation, characterization and evaluation of microsatellite DNA markers in the giant freshwater prawn, Marcrobrachium rosenbergii, from South India.Aquaculture284481284
- 18. See LM, Tan SG, Hassan R, Siraj SS, Bhassu S (2009) Development of microsatellite markers from an enriched genomic library for the genetic analysis of the Malaysian giant freshwater prawn, Macrobrachium rosenbergii. Biochem Genet 47: 722–726.LM SeeSG TanR. HassanSS SirajS. Bhassu2009Development of microsatellite markers from an enriched genomic library for the genetic analysis of the Malaysian giant freshwater prawn, Macrobrachium rosenbergii.Biochem Genet47722726
- 19. Miller AD, Murphy NP, Burridge CP, Austin CM (2005) Complete mitochondrial DNA sequences of the Decapod Crustaceans Pseudocarcinus gigas (Menippidae) and Marcrobrachium rosenbergii (Palaemonidae). Mar Biotechnol 7: 339–349.AD MillerNP MurphyCP BurridgeCM Austin2005Complete mitochondrial DNA sequences of the Decapod Crustaceans Pseudocarcinus gigas (Menippidae) and Marcrobrachium rosenbergii (Palaemonidae).Mar Biotechnol7339349
- 20. de Bruyn M, Wilson JC, Mather PB (2004) Huxley's line demarcates extensive genetic divergence between eastern and western forms of the giant freshwater prawn, Marcrobrachium rosenbergii. Mol Phylogenet Evol 30: 251–257.M. de BruynJC WilsonPB Mather2004Huxley's line demarcates extensive genetic divergence between eastern and western forms of the giant freshwater prawn, Marcrobrachium rosenbergii.Mol Phylogenet Evol30251257
- 21. de Bruyn M, Mather PB (2007) Molecular signatures of Pleistocene sea-level changes that affected connectivity among freshwater shrimp in Indo-Australian waters. Mol Ecol 16: 4295–4307.M. de BruynPB Mather2007Molecular signatures of Pleistocene sea-level changes that affected connectivity among freshwater shrimp in Indo-Australian waters.Mol Ecol1642954307
- 22. Baruah K, Cam DTV, Dierckens K, Wille M, Defoirdt T, et al. (2009) In vivo effects single or combined N-acyl homoserine lactone quorum sensing signals on the performance of Marcrobrachium rosenbergii larvae. Aquaculture 288: 233–238.K. BaruahDTV CamK. DierckensM. WilleT. Defoirdt2009In vivo effects single or combined N-acyl homoserine lactone quorum sensing signals on the performance of Marcrobrachium rosenbergii larvae.Aquaculture288233238
- 23. Cam DTV, Nhan DT, Ceuppens S, Hao NV, Dierckens K, et al. (2009) Effect of N-acyl homoserine lactone-degrading enrichment cultures on Marcrobrachium rosenbergii larviculture. Aquaculture 294: 5–13.DTV CamDT NhanS. CeuppensNV HaoK. Dierckens2009Effect of N-acyl homoserine lactone-degrading enrichment cultures on Marcrobrachium rosenbergii larviculture.Aquaculture294513
- 24. Sung HH, Yang CW, Lin YH, Chang PT (2009) The effect of two CpG oligodeoxynucleotides with different sequences on haemocytic immune responses of giant freshwater prawn, Macrobrachium rosenbergii. Fish Shellfish Immunol 26: 256–263.HH SungCW YangYH LinPT Chang2009The effect of two CpG oligodeoxynucleotides with different sequences on haemocytic immune responses of giant freshwater prawn, Macrobrachium rosenbergii.Fish Shellfish Immunol26256263
- 25. Ngernsoungnern P, Ngernsoungnern A, Weerachatyanukul W, Meeratana P, Hanna PJ, et al. (2009) Abalone egg-laying hormone induces rapid ovarian maturation and early spawning of giant freshwater prawn, Macrobrachium rosenbergii. Aquaculture 296: 143–149.P. NgernsoungnernA. NgernsoungnernW. WeerachatyanukulP. MeeratanaPJ Hanna2009Abalone egg-laying hormone induces rapid ovarian maturation and early spawning of giant freshwater prawn, Macrobrachium rosenbergii.Aquaculture296143149
- 26. Vera JC, Wheat CW, Fescemyer HW, Frilander MJ, Crawford DL, et al. (2008) Rapid transcriptome characterization for a nonmodel organism using 454 pyrosequencing. Mol Ecol 17: 1636–1647.JC VeraCW WheatHW FescemyerMJ FrilanderDL Crawford2008Rapid transcriptome characterization for a nonmodel organism using 454 pyrosequencing.Mol Ecol1716361647
- 27. Wheat CW (2008) Rapidly developing functional genomics in ecological model systems via 454 transcriptome sequencing. Genetica 138: 433–451.CW Wheat2008Rapidly developing functional genomics in ecological model systems via 454 transcriptome sequencing.Genetica138433451
- 28. Bai X, Mamidala , Rajarapu SP, Jones SC, Mittapalli O (2011) Transcriptomics of the bed bug (Climex lectularius). PLoS One 6: e16336.X. BaiMamidalaSP RajarapuSC JonesO. Mittapalli2011Transcriptomics of the bed bug (Climex lectularius).PLoS One6e16336
- 29. Bai X, Rivera-Vega L, Mamidala P, Bonello P, Herms DA et al (2011) Transcriptomic signature of ash (Fraxinus spp.) phloem. PLoS One 6: e16368.X. BaiL. Rivera-VegaP. MamidalaP. Bonelloal Herms DA et2011Transcriptomic signature of ash (Fraxinus spp.) phloem.PLoS One6e16368
- 30. Margulies M, Egholm M, Altman WE, Attiya S, Bader JS, et al. (2005) Genome sequencing in microfabricated high-density picolitre reactions. Nature 437: 376–380.M. MarguliesM. EgholmWE AltmanS. AttiyaJS Bader2005Genome sequencing in microfabricated high-density picolitre reactions.Nature437376380
- 31. Emrich SJ, Barbazuk WB, Li L, Schnable PS (2007) Gene discovery and annotation using LCM-454 transcriptome sequencing. Genome Res 17: 69–73.SJ EmrichWB BarbazukL. LiPS Schnable2007Gene discovery and annotation using LCM-454 transcriptome sequencing.Genome Res176973
- 32. Novaes E, Drost DR, Farmerie WG, Pappas GJ Jr, Grattapaglia D, et al. (2008) High-throughput gene and SNP discovery in Eucalyptus grandis, and uncharacterized genome. BMC Genomics 9: 312.E. NovaesDR DrostWG FarmerieGJ Pappas JrD. Grattapaglia2008High-throughput gene and SNP discovery in Eucalyptus grandis, and uncharacterized genome.BMC Genomics9312
- 33. Parchman TL, Geist KS, Grahnen JA, Benkman CW, Buerkle CA (2010) Transcriptome sequencing in an ecologically important tree species: assembly, annotation, and marker discovery. BMC Genomics 11: 180.TL ParchmanKS GeistJA GrahnenCW BenkmanCA Buerkle2010Transcriptome sequencing in an ecologically important tree species: assembly, annotation, and marker discovery.BMC Genomics11180
- 34. Wang J-PZ, Lindsay BG, Leebens-Mack J, Cui L, Wall K, et al. (2004) EST clustering error evaluation and correction. Bioinformatics 20: 2973–2984.J-PZ WangBG LindsayJ. Leebens-MackL. CuiK. Wall2004EST clustering error evaluation and correction.Bioinformatics2029732984
- 35. Liang H, Carlson JE, Leebens-Mack JH, Wall PK, Mueller LA, et al. (2008) An EST database for Liriodendron tulipifera L. floral buds: the first EST resource for functional and comparative genomics in Liriodendrom. Tree Genet Genom 4: 419–433.H. LiangJE CarlsonJH Leebens-MackPK WallLA Mueller2008An EST database for Liriodendron tulipifera L. floral buds: the first EST resource for functional and comparative genomics in Liriodendrom.Tree Genet Genom4419433
- 36. Mittapalli O, Bai X, Mamidala P, Rajarapu SP, Bonello P, et al. (2010) Tissue-specific transcriptomics of the exotic invasive insect pest emerald ash borer. PLoS One 5: e13708.O. MittapalliX. BaiP. MamidalaSP RajarapuP. Bonello2010Tissue-specific transcriptomics of the exotic invasive insect pest emerald ash borer.PLoS One5e13708
- 37. Hale MC, McCormick CR, Jackson JR, DeWoody JA (2009) Next-generation pyrosequencing of gonad transcriptomes in the polyploidy lake sturgeon (Acipenser fulvescens): the relative merits of normalization and rarefaction in gene discovery. BMC Genomics 10: 203.MC HaleCR McCormickJR JacksonJA DeWoody2009Next-generation pyrosequencing of gonad transcriptomes in the polyploidy lake sturgeon (Acipenser fulvescens): the relative merits of normalization and rarefaction in gene discovery.BMC Genomics10203
- 38. Hale MC, Jackson JR, DeWoody JA (2010) Discovery and evaluation of candidate sex-determining genes and xenobiotics in the gonads of lake sturgeon (Acipenser fulvescens). Genetica 138: 745–456.MC HaleJR JacksonJA DeWoody2010Discovery and evaluation of candidate sex-determining genes and xenobiotics in the gonads of lake sturgeon (Acipenser fulvescens).Genetica138745456
- 39. Hooper SL, Thuma JB (2005) Invertebrate muscles: muscle specific genes and proteins. Physiol Rev 85: 1001–1060.SL HooperJB Thuma2005Invertebrate muscles: muscle specific genes and proteins.Physiol Rev8510011060
- 40. Zhu X, Dai Z, Liu J, Yang W (2005) Actin gene in prawn, Macrobrachium rosenbergii: Characteristics and differential tissue expression during embryonic development. Comp Biochem Physiol B Biochem Mol Biol 140: 599–605.X. ZhuZ. DaiJ. LiuW. Yang2005Actin gene in prawn, Macrobrachium rosenbergii: Characteristics and differential tissue expression during embryonic development.Comp Biochem Physiol B Biochem Mol Biol140599605
- 41. Hooper SL, Hobbs KH, Thuma JB (2008) Invertebrate muscles: thin and thick filament structure; molecular basis of contraction and its regulation, catch and asynchronous muscle. Prog Neurobiol 86: 72–127.SL HooperKH HobbsJB Thuma2008Invertebrate muscles: thin and thick filament structure; molecular basis of contraction and its regulation, catch and asynchronous muscle.Prog Neurobiol8672127
- 42. Kim BK, Kim KS, Oh C, Mykles DL, Lee SG, et al. (2009) Twelve actin-encoding cDNAs from the American lobster, Homarus americanus: Cloning and tissue expression of eight skeletal muscle, one heart, and three cytoplasmic isoforms. Comp Biochem Physiol B Biochem Mol Biol 153: 178–184.BK KimKS KimC. OhDL MyklesSG Lee2009Twelve actin-encoding cDNAs from the American lobster, Homarus americanus: Cloning and tissue expression of eight skeletal muscle, one heart, and three cytoplasmic isoforms.Comp Biochem Physiol B Biochem Mol Biol153178184
- 43. Leelatanawit R, Sittikankeaw K, Yocawibun P, Klinbunga S, et al. (2009) Identification, characterization and expression of sex-related genes in testes of the giant tiger shrimp Penaeus monodon. Comp Biochem Physiol A Mol Integr Physiol 152: 66–76.R. LeelatanawitK. SittikankeawP. YocawibunS. Klinbunga2009Identification, characterization and expression of sex-related genes in testes of the giant tiger shrimp Penaeus monodon.Comp Biochem Physiol A Mol Integr Physiol1526676
- 44. Minet-Quinard R, Moinard C, Villie F, Vasson MP, Cynober L (2004) Metabolic pathways implicated in the kinetic impairment of muscle glutamine homeostasis in adult and old glucocorticoid-treated rats. Am J Physiol Endocrinol Metab 287: E671–676.R. Minet-QuinardC. MoinardF. VillieMP VassonL. Cynober2004Metabolic pathways implicated in the kinetic impairment of muscle glutamine homeostasis in adult and old glucocorticoid-treated rats.Am J Physiol Endocrinol Metab287E671676
- 45. Huber K, Miles JL, Norman AM, Thompson NM, Davison M, et al. (2009) Prenatally induced changes in muscle structure and metabolic function facilitate exercise-induced obesity prevention. Endorinology 150: 4135–4144.K. HuberJL MilesAM NormanNM ThompsonM. Davison2009Prenatally induced changes in muscle structure and metabolic function facilitate exercise-induced obesity prevention.Endorinology15041354144
- 46. Lesser MP (2006) Oxidative stress in marine environments: Biochemistry and physiological ecology. Annu Rev Physiol 68: 253–278.MP Lesser2006Oxidative stress in marine environments: Biochemistry and physiological ecology.Annu Rev Physiol68253278
- 47. Gnaiger E, Méndez G, Hand SC (2000) High phosphorylation efficiency and depression of uncoupled respiration in mitochondria under hypoxia. PNAS 97: 11080–11085.E. GnaigerG. MéndezSC Hand2000High phosphorylation efficiency and depression of uncoupled respiration in mitochondria under hypoxia.PNAS971108011085
- 48. Vogt T (2010) Pnenylpropanoid biosynthesis. Mol Plant 3: 2–20.T. Vogt2010Pnenylpropanoid biosynthesis.Mol Plant3220
- 49. Ferrer JL, Austin MB, Stewart C Jr, Noel JP (2008) Structure and function of enzyme involved in the biosynthesis of phenylpropanoids. Plant Physiol Biochem 46: 356–370.JL FerrerMB AustinC. Stewart JrJP Noel2008Structure and function of enzyme involved in the biosynthesis of phenylpropanoids.Plant Physiol Biochem46356370
- 50. Hagel JM, Weljie AM, Vogel HJ, Facchini PJ (2008) Quantitative 1H nuclear magnetic resonance metabolite profiling as a functional genomics platform to investigate alkaloid biosynthesis in Opium Poppy. Plant Physiol 147: 1805–1821.JM HagelAM WeljieHJ VogelPJ Facchini2008Quantitative 1H nuclear magnetic resonance metabolite profiling as a functional genomics platform to investigate alkaloid biosynthesis in Opium Poppy.Plant Physiol14718051821
- 51. Ziegler J, Facchini PJ (2008) Alkaloid biosythensis: metabolism and trafficking. Annu Rev Plant Biol 59: 735–769.J. ZieglerPJ Facchini2008Alkaloid biosythensis: metabolism and trafficking.Annu Rev Plant Biol59735769
- 52. Kashman Y, Bishara A, Aknin M (2010) Recent N-atom containing compounds from Indo-Pacific invertebrates. Mar Drugs 8: 2810–2836.Y. KashmanA. BisharaM. Aknin2010Recent N-atom containing compounds from Indo-Pacific invertebrates.Mar Drugs828102836
- 53. McNeil GP, Schroeder AJ, Roberts MA, Jackson FR (2001) Genetic analysis of functional domains within the Drosophila LARK RNA-binding protein. Genetics 159: 229–240.GP McNeilAJ SchroederMA RobertsFR Jackson2001Genetic analysis of functional domains within the Drosophila LARK RNA-binding protein.Genetics159229240
- 54. Sutherland LC, Rintala-Maki ND, White RD, Morin CD (2005) RNA binding motif (RBM) proteins: a novel family of apoptosis modulators? J Cell Biochem 94: 5–24.LC SutherlandND Rintala-MakiRD WhiteCD Morin2005RNA binding motif (RBM) proteins: a novel family of apoptosis modulators?J Cell Biochem94524
- 55. Bouhouche N, Syvanen M, Kado CI (2002) The origin of prokaryotic C2H2 zinc finger regulators. Trends Microbiol 8: 77–81.N. BouhoucheM. SyvanenCI Kado2002The origin of prokaryotic C2H2 zinc finger regulators.Trends Microbiol87781
- 56. Wolfe Sa, Nekludova L, Pabo CO (2000) DNA recognition by Cys2His2 zinc finger proteins. Annu Rev Biophys Biomol Struct 29: 183–212.Sa WolfeL. NekludovaCO Pabo2000DNA recognition by Cys2His2 zinc finger proteins.Annu Rev Biophys Biomol Struct29183212
- 57. Brayer KJ, Segal DJ (2008) Keep your fingers off my DNA: protein-protein interactions mediated by C2H2 zinc finger domains. Cell Biochem Biophys 50: 111–131.KJ BrayerDJ Segal2008Keep your fingers off my DNA: protein-protein interactions mediated by C2H2 zinc finger domains.Cell Biochem Biophys50111131
- 58. Bochkarev A, Barwell JA, Pfuetzner RA, Furey W , Edwards AM, et al. (1995) Crystal structure of the DNA-binding domain of the Epstein-Barr virus origin-binding protein EBNA 1. Cell 83: 39–46.A. BochkarevJA BarwellRA PfuetznerFurey W JrAM Edwards1995Crystal structure of the DNA-binding domain of the Epstein-Barr virus origin-binding protein EBNA 1.Cell833946
- 59. Kielkopf CL, Lucke S, Green MR (2004) U2AF homology motifs: protein recognition in the RRM world. Genes Dev 18: 1513–1526.CL KielkopfS. LuckeMR Green2004U2AF homology motifs: protein recognition in the RRM world.Genes Dev1815131526
- 60. Kraemer B, Crittenden S, Gallegos M, Moulder G, Barstead R, et al. (1999) NANOS-3 and FBF proteins physically interact to control the sperm-oocyte switch in Caenorhabditis elegans. Curr Bio 9: 1009–1018.B. KraemerS. CrittendenM. GallegosG. MoulderR. Barstead1999NANOS-3 and FBF proteins physically interact to control the sperm-oocyte switch in Caenorhabditis elegans.Curr Bio910091018
- 61. Li D, Roberts R (2001) WD-repeat proteins: structure characteristics, biological function, and their involvement in human diseases. Cell Mol Life Sci 58: 2085–2097.D. LiR. Roberts2001WD-repeat proteins: structure characteristics, biological function, and their involvement in human diseases.Cell Mol Life Sci5820852097
- 62. Smith TF, Gaitatzes C, Saxena K, Neer EJ (1999) The WD repeat: a common architecture for diverse functions. Trends Biochem Sci 24: 181–1885.TF SmithC. GaitatzesK. SaxenaEJ Neer1999The WD repeat: a common architecture for diverse functions.Trends Biochem Sci241811885
- 63. Bourne HR, Sanders DA, McCormick F (1990) The GTPase superfamily: a conserved switch for diverse cell functions. Nature 348: 125–132.HR BourneDA SandersF. McCormick1990The GTPase superfamily: a conserved switch for diverse cell functions.Nature348125132
- 64. Bourne HR, Sander DA, McCormick F (1991) The GTPase superfamily: conserved structure and molecular mechanism. Nature 349: 117–127.HR BourneDA SanderF. McCormick1991The GTPase superfamily: conserved structure and molecular mechanism.Nature349117127
- 65. Scheffzek K, Klebe C, Fritz-Wolf K, Kabsch W, Wittinghofer A (1995) Crystal structure of the nuclear Ras-related protein Ran in its GDP-bond form. Nature 374: 378–381.K. ScheffzekC. KlebeK. Fritz-WolfW. KabschA. Wittinghofer1995Crystal structure of the nuclear Ras-related protein Ran in its GDP-bond form.Nature374378381
- 66. Rush MG, Drivas G, D'Eustaschi P (1996) The small nuclear GTPase Ran: how much does it run? Bioessays 18: 103–112.MG RushG. DrivasP. D'Eustaschi1996The small nuclear GTPase Ran: how much does it run?Bioessays18103112
- 67. Teichmann SA, Chothia C (2000) Immunoglobulin superfamily proteins in Caenorhabditis elegans. J Mol Biol 296: 1367–1383.SA TeichmannC. Chothia2000Immunoglobulin superfamily proteins in Caenorhabditis elegans.J Mol Biol29613671383
- 68. Potapov V, Sobolev V, Edelman M, Kister A, Gelfand I (2004) Protein-protein recognition: juxtaposition of domain and interface cores in immunoglobulins and other sandwich-like proteins. J Mol Biol 342: 665–679.V. PotapovV. SobolevM. EdelmanA. KisterI. Gelfand2004Protein-protein recognition: juxtaposition of domain and interface cores in immunoglobulins and other sandwich-like proteins.J Mol Biol342665679
- 69. Su J, Oanh DTH, Lyons RE, Leeton L, van Hulten MCW, et al. (2008) A key gene of RNA interference pathway in the black tiger shrimp, Penaeus monodo: Identification and fuctional characterization of Dicer-1. Fish Shellfish Immunol 24: 223–233.J. SuDTH OanhRE LyonsL. LeetonMCW van Hulten2008A key gene of RNA interference pathway in the black tiger shrimp, Penaeus monodo: Identification and fuctional characterization of Dicer-1.Fish Shellfish Immunol24223233
- 70. Dechklar M, Udomkit A, Panyim S (2008) Characterization of argonaute cDNA from Penaeus monodon and implication of its role in RNA interference. Biochem Biophys Res Commun 367: 768–774.M. DechklarA. UdomkitS. Panyim2008Characterization of argonaute cDNA from Penaeus monodon and implication of its role in RNA interference.Biochem Biophys Res Commun367768774
- 71. Wu Q, Luo Y, Lu R, Lau N, Lai EC, et al. (2010) Virus discovery by deep sequencing and assembly of virus-derived small silencing RNAs. PNAS 107: 1606–1611.Q. WuY. LuoR. LuN. LauEC Lai2010Virus discovery by deep sequencing and assembly of virus-derived small silencing RNAs.PNAS10716061611
- 72. Soonthornchai W, Rungrassamee W, Karoonuthaisiri N, Jarayabhand P, Klingunga S, et al. (2010) Expression of immune-related genes in the digestive organ of shrimp, Penaeus monodon, after an oral infection by Vibrio harveyi. Dev Comp Immunol 34: 19–28.W. SoonthornchaiW. RungrassameeN. KaroonuthaisiriP. JarayabhandS. Klingunga2010Expression of immune-related genes in the digestive organ of shrimp, Penaeus monodon, after an oral infection by Vibrio harveyi.Dev Comp Immunol341928
- 73. Kabsch W, Vandekerckhove J (1992) Structure and function of actin. Annu Rev Biophys Biomol Struct 21: 49–76.W. KabschJ. Vandekerckhove1992Structure and function of actin.Annu Rev Biophys Biomol Struct214976
- 74. Dominguez R, Holmes K (2011) Actin structure and function. Annu Rev Biophysics 40: 169–186.R. DominguezK. Holmes2011Actin structure and function.Annu Rev Biophysics40169186
- 75. Hayashida M, Maita T, Matsuda G (1991) The primary structure of skeletal muscle myosin heavy chain: I. Sequences of amino-terminal 23 kDa fragment. J Biochem 110: 54–59.M. HayashidaT. MaitaG. Matsuda1991The primary structure of skeletal muscle myosin heavy chain: I. Sequences of amino-terminal 23 kDa fragment.J Biochem1105459
- 76. Schiaffino S, Reggiani C (1996) Molecular diversity of myofibrillar proteins: gene regulation and functional significance. Physiol Rev 76: 371–423.S. SchiaffinoC. Reggiani1996Molecular diversity of myofibrillar proteins: gene regulation and functional significance.Physiol Rev76371423
- 77. DeNardi C, Ausoni S, Moretti P, Gorza L, Velleca M, et al. (1993) Type 2X-myopsin heavy chain is coded by a muscle fiber type-specific and developmentally regulated gene. J Cell Biol 123: 823–835.C. DeNardiS. AusoniP. MorettiL. GorzaM. Velleca1993Type 2X-myopsin heavy chain is coded by a muscle fiber type-specific and developmentally regulated gene.J Cell Biol123823835
- 78. Jung HH, Lieber RL, Ryan AF (1998) Quantification of myosin heavy chain mRNA in somatic and brachial arch muscles using competitive PCR. Am J Physiol 275: 68–74.HH JungRL LieberAF Ryan1998Quantification of myosin heavy chain mRNA in somatic and brachial arch muscles using competitive PCR.Am J Physiol2756874
- 79. Kamimura MT, Meier KM, Cavalli RO, Laurino J, Maggioni R, et al. (2008) Characterization of growth-related genes in the south-western Atlantic pink shrimp Farfantepenaeus paulensis (Pérez-Farfante 1967) through a modified DDRT-PCR protocol. Aqua Res 39: 200–204.MT KamimuraKM MeierRO CavalliJ. LaurinoR. Maggioni2008Characterization of growth-related genes in the south-western Atlantic pink shrimp Farfantepenaeus paulensis (Pérez-Farfante 1967) through a modified DDRT-PCR protocol.Aqua Res39200204
- 80. Medler S, Lilley T, Mykles DL (2004) Fiber polymorphism in skeletal muscles of the American lobster, Homarus americanus: continuum between slow-twitch (S1) and slow-tonic (S2) fibers. J Exp Biol 207: 2755–2767.S. MedlerT. LilleyDL Mykles2004Fiber polymorphism in skeletal muscles of the American lobster, Homarus americanus: continuum between slow-twitch (S1) and slow-tonic (S2) fibers.J Exp Biol20727552767
- 81. Medler S, Brown KJ, Chang ES, Mykles DL (2005) Myosin heavy chain gene expression in adult lobster skeletal muscles. Biol Bull 208: 127–137.S. MedlerKJ BrownES ChangDL Mykles2005Myosin heavy chain gene expression in adult lobster skeletal muscles.Biol Bull208127137
- 82. Abdel Rahman AM, Kamath S, Lopata AL, Helleur RJ (2010) Analysis of the allergenic proteins in black prawn (Penaeus monodon) and characterization of the major allergen tropomyopsin using mass spectrometry. Rapid Commun Mass Spectrom 24: 2462–2470.AM Abdel RahmanS. KamathAL LopataRJ Helleur2010Analysis of the allergenic proteins in black prawn (Penaeus monodon) and characterization of the major allergen tropomyopsin using mass spectrometry.Rapid Commun Mass Spectrom2424622470
- 83. Perry MJ, Tait J, Hu J, White SC, Medler S (2009) Skeletal muscle fiber types in the ghost crab, Ocypode quadrata: implications for running performance. J Exp Biol 212: 673–683.MJ PerryJ. TaitJ. HuSC WhiteS. Medler2009Skeletal muscle fiber types in the ghost crab, Ocypode quadrata: implications for running performance.J Exp Biol212673683
- 84. MacLeod AR (1987) Genetic origin of diversity of human cytoskeletal tropomyosins. Bioessays 6: 208–212.AR MacLeod1987Genetic origin of diversity of human cytoskeletal tropomyosins.Bioessays6208212
- 85. Wolska BM, Wieczorek DM (2003) The role of tropomosin in the regulation of myocardial contraction and relaxation. Pflugers Arch 446: 1–8.BM WolskaDM Wieczorek2003The role of tropomosin in the regulation of myocardial contraction and relaxation.Pflugers Arch44618
- 86. Strasser P, Gimona M, Moessler H, Herzog M, Small JV (1993) Mammalian calponin: Identification and expression of genetic variants. LEBS Lett 330: 13–18.P. StrasserM. GimonaH. MoesslerM. HerzogJV Small1993Mammalian calponin: Identification and expression of genetic variants.LEBS Lett3301318
- 87. Meyer-Rochow VB, Royuela M (2002) Calponin, caldesmon, and chromatophores: The smooth muscle connection. Microsc Res Tech 58: 504–513.VB Meyer-RochowM. Royuela2002Calponin, caldesmon, and chromatophores: The smooth muscle connection.Microsc Res Tech58504513
- 88. Prinjha RK, Shapland CE, Hsuan JJ, Totty NF, Mason JJ, et al. (1994) Cloning and sequencing of cDNAs encoding the actin cross-linking protein transgelin defines a new family of actin-associated proteins. Cell Motil Cytoskeleton 28: 243–255.RK PrinjhaCE ShaplandJJ HsuanNF TottyJJ Mason1994Cloning and sequencing of cDNAs encoding the actin cross-linking protein transgelin defines a new family of actin-associated proteins.Cell Motil Cytoskeleton28243255
- 89. Solway J, Seltzer J, Samaha FF, Kim S, Alger LE, et al. (1995) Structure and expression of a smooth cell-specific gene, SM22 alpha. J Biol Chem 270: 13460–13469.J. SolwayJ. SeltzerFF SamahaS. KimLE Alger1995Structure and expression of a smooth cell-specific gene, SM22 alpha.J Biol Chem2701346013469
- 90. Belfiore M, Pugnale P, Saudan Z, Puoti A (2004) Roles of the C. elegans cyclophilin like protein MOG-6 in MEP-1 binding and germline fates. Development 131: 2935–2945.M. BelfioreP. PugnaleZ. SaudanA. Puoti2004Roles of the C. elegans cyclophilin like protein MOG-6 in MEP-1 binding and germline fates.Development13129352945
- 91. Towers GJ (2007) The control of viral infection by tripartite motif proteins and cyclophilin A. Retrovirology 4: 40–50.GJ Towers2007The control of viral infection by tripartite motif proteins and cyclophilin A. Retrovirology44050
- 92. Tangprasittipap A, Tiensuwan M, Withyachumnarnkul B (2010) Characterization of candidate genes involved in growth of black tiger shrimp. Aquaculture 307: 150–156.A. TangprasittipapM. TiensuwanB. Withyachumnarnkul2010Characterization of candidate genes involved in growth of black tiger shrimp.Aquaculture307150156
- 93. Zimmerman AW, Veerkamp JH (2002) New insights into the structure and function of fatty acid-binding proteins. Cell Mol Life Sci 59: 1096–1116.AW ZimmermanJH Veerkamp2002New insights into the structure and function of fatty acid-binding proteins.Cell Mol Life Sci5910961116
- 94. Esteves A, Ehrlich R (2006) Invertebrate intracellular fatty acid binding proteins. Comp Biochem Physiol C Toxicol Pharmacol 2: 262–274.A. EstevesR. Ehrlich2006Invertebrate intracellular fatty acid binding proteins.Comp Biochem Physiol C Toxicol Pharmacol2262274
- 95. Haunerland NH, Xinmei Ch, Andolfatto P, Chisholm JM, Wang Z (1993) Developmental changes of FABP concentration, expression and intracellular distribution in locust flight muscle. Mol Cell Biochem 123: 153–158.NH HaunerlandCh XinmeiP. AndolfattoJM ChisholmZ. Wang1993Developmental changes of FABP concentration, expression and intracellular distribution in locust flight muscle.Mol Cell Biochem123153158
- 96. Van der Horst DJ (1990) Lipid transport functions of lipoproteins in flying insects. Biochim Biophys Acta 1047: 195–211.DJ Van der Horst1990Lipid transport functions of lipoproteins in flying insects.Biochim Biophys Acta1047195211
- 97. Bach I (2002) The LIM domain: regulation by association. Mech Dev 91: 5–17.I. Bach2002The LIM domain: regulation by association.Mech Dev91517
- 98. Barat-Houari M, Clément K, Vatin V, Dina C, Bonhomme G, et al. (2002) Positional candidate gene analysis of Lim domain homeobox gene (Isl-1) on chromosome 5q11–q13 in a French morbidly obese population suggests indication for association with type 2 diabetes. Diabetes 51: 1640–1643.M. Barat-HouariK. ClémentV. VatinC. DinaG. Bonhomme2002Positional candidate gene analysis of Lim domain homeobox gene (Isl-1) on chromosome 5q11–q13 in a French morbidly obese population suggests indication for association with type 2 diabetes.Diabetes5116401643
- 99. Postel U, Thompson F, Barker G, Viney Mm Morris S (2010) Migration-related changes in gene expression in leg muscle of the Christmas Island red crab Gecarcoidea natalis: seasonal preparation for long-distance walking. J Exp Biol 213: 1740–1750.U. PostelF. ThompsonG. BarkerS. Viney Mm Morris2010Migration-related changes in gene expression in leg muscle of the Christmas Island red crab Gecarcoidea natalis: seasonal preparation for long-distance walking.J Exp Biol21317401750
- 100. Ibrahim RK, Bruneau A, Bantignies B (1998) Plant o-methyltransferase: molecular analysis, common signature and classification. Plant Mol Biol 36: 1–10.RK IbrahimA. BruneauB. Bantignies1998Plant o-methyltransferase: molecular analysis, common signature and classification.Plant Mol Biol36110
- 101. Kuballa A, Guyatt K, Dixon B, Thaggard H, Ashton AR, et al. (2007) Isolation and expression analysis of multiple isoforms of putative farnesoic acid O-methyltransferase in several crustacean species. Gen Comp Endocrinol 150: 48–58.A. KuballaK. GuyattB. DixonH. ThaggardAR Ashton2007Isolation and expression analysis of multiple isoforms of putative farnesoic acid O-methyltransferase in several crustacean species.Gen Comp Endocrinol1504858
- 102. Borst DW, Laufer M, Landau ES, Chang WA, Hertz FC, et al. (1987) Methyl farnesoate (MF) and its role in crustacean reproduction and development. Insect Biochem 17: 1123–1127.DW BorstM. LauferES LandauWA ChangFC Hertz1987Methyl farnesoate (MF) and its role in crustacean reproduction and development.Insect Biochem1711231127
- 103. Laufer H, Borst DW, Baker FC, Carrasco C, Sinkus M, et al. (1987) Identification of a juvenile hormone-like compound in a crustacean. Science 235: 202–205.H. LauferDW BorstFC BakerC. CarrascoM. Sinkus1987Identification of a juvenile hormone-like compound in a crustacean.Science235202205
- 104. Tamone SL, Prestwich GD, Chang ES (1997) Identification and characterization of methyl farnesoate binding proteins from the crab, Cancer magister. Gen Comp Endocrinol 105: 168–175.SL TamoneGD PrestwichES Chang1997Identification and characterization of methyl farnesoate binding proteins from the crab, Cancer magister.Gen Comp Endocrinol105168175
- 105. Laufer H, Landau M, Homola E, Borst W (1987) Methyl farnesoate: its site of synthesis and regulation of secretion in a juvenile crustacean. Insect Biochem 17: 1129–1131.H. LauferM. LandauE. HomolaW. Borst1987Methyl farnesoate: its site of synthesis and regulation of secretion in a juvenile crustacean.Insect Biochem1711291131
- 106. Sagi A, Homola E, Laufer H (1991) Methyl farnesoate in the prawn Macrobrachium rosenbergii: synthesis by the mandibular organ in vitro, and titers in the hemolymph. Comp Biochem Physiol B 99: 879–882.A. SagiE. HomolaH. Laufer1991Methyl farnesoate in the prawn Macrobrachium rosenbergii: synthesis by the mandibular organ in vitro, and titers in the hemolymph.Comp Biochem Physiol B99879882
- 107. Wang Z, Ding Q, Yagi KJ, Tobe SS (1994) Terminal stages in juvenile hormone biosynthesis in corpora allata of Diploptera punctata: development changes in enzyme activity and regulation by allatostatins. J Insect Physiol 40: 217–223.Z. WangQ. DingKJ YagiSS Tobe1994Terminal stages in juvenile hormone biosynthesis in corpora allata of Diploptera punctata: development changes in enzyme activity and regulation by allatostatins.J Insect Physiol40217223
- 108. Feyereisen R, Friedel Tobe SS (1981) Farnesoic acid stimulation of C16 juvenile hormone biosynthesis by corpora allata of adult female Diploptera punctata. Insect Biochem 11: 401–409.R. FeyereisenSS Friedel Tobe1981Farnesoic acid stimulation of C16 juvenile hormone biosynthesis by corpora allata of adult female Diploptera punctata.Insect Biochem11401409
- 109. Gunawardene YI, Bendena WG, Tobe SS, Chana SM (2003) Comparative immunohistochemistry and cellular distribution of farnesoic acid O-methyltransferase in the shrimp and the crayfish. Peptides 24: 1591–1597.YI GunawardeneWG BendenaSS TobeSM Chana2003Comparative immunohistochemistry and cellular distribution of farnesoic acid O-methyltransferase in the shrimp and the crayfish.Peptides2415911597
- 110. Ruddell CJ, Wainwright G, Geffen A, White MR, Webster SG, et al. (2003) Cloning, characterization and developmental expression of a putative farnesoic acid O-methyltransferase in the female edible crab Cancer pagurus. Biol Bull 205: 308–318.CJ RuddellG. WainwrightA. GeffenMR WhiteSG Webster2003Cloning, characterization and developmental expression of a putative farnesoic acid O-methyltransferase in the female edible crab Cancer pagurus.Biol Bull205308318
- 111. Holford KC, Edwards KA, Bendena WG, Tobe SS, Wang Z, et al. (2004) Purification and characterization of a mandibular organ protein from the American lobster, Homarus americanus: a putative farnesoic acid O-methyltransferase. Insect Biochem Mol Biol 34: 785–798.KC HolfordKA EdwardsWG BendenaSS TobeZ. Wang2004Purification and characterization of a mandibular organ protein from the American lobster, Homarus americanus: a putative farnesoic acid O-methyltransferase.Insect Biochem Mol Biol34785798
- 112. Hui JH, Tobe SS, Chan SM (2008) Characterization of the putative farnesoic acid O-methyltransferase (LvFAMeT) cDNA from white shrimp, Litopenaeus vannamei: Evidence for its role in molting. Peptides 29: 252–260.JH HuiSS TobeSM Chan2008Characterization of the putative farnesoic acid O-methyltransferase (LvFAMeT) cDNA from white shrimp, Litopenaeus vannamei: Evidence for its role in molting.Peptides29252260
- 113. Critchley DR, Hold MR, Barry ST, Priddle H, Hemmings L, et al. Integrin-mediated cell adhesion: the cytoskeletal connection. Biochem Soc Symp 65: 79–99.DR CritchleyMR HoldST BarryH. PriddleL. HemmingsIntegrin-mediated cell adhesion: the cytoskeletal connection.Biochem Soc Symp657999
- 114. Pollard TD (2008) Progress towards understanding the mechanism of cytokinesis in fission yeast. Biochem Soc Trans 36: 425–430.TD Pollard2008Progress towards understanding the mechanism of cytokinesis in fission yeast.Biochem Soc Trans36425430
- 115. Buss F, Temm-Grove C, Henning S, Jockusch BM (1992) Distribution of profiling in fibroblasts correlates with the presence of highly dynamic actin filaments. Cell Motil Cytoskeleton 22: 51–61.F. BussC. Temm-GroveS. HenningBM Jockusch1992Distribution of profiling in fibroblasts correlates with the presence of highly dynamic actin filaments.Cell Motil Cytoskeleton225161
- 116. Witke W, Podtelejnikov AV, Di Nardo A, Sutherland JD, Gurniak CB, et al. (1998) In mouse brain profilin I and profilin II associate with regulators of the endocytic pathway and actin assembly. EMBO J 17: 967–976.W. WitkeAV PodtelejnikovA. Di NardoJD SutherlandCB Gurniak1998In mouse brain profilin I and profilin II associate with regulators of the endocytic pathway and actin assembly.EMBO J17967976
- 117. Rawe VY, Payne C, Schatten G (2006) Profilin and actin-related proteins regulate microfilament dynamics during early mammalian embryogenesis. Hum Reprod 21: 1143–1153.VY RaweC. PayneG. Schatten2006Profilin and actin-related proteins regulate microfilament dynamics during early mammalian embryogenesis.Hum Reprod2111431153
- 118. Birbach A (2008) Profilin, a multi-modal regulator of neuronal plasticity. BioEssays 30: 994–1002.A. Birbach2008Profilin, a multi-modal regulator of neuronal plasticity.BioEssays309941002
- 119. Magdolen V, Oechsner U, Muller G, Bandlow W (1988) The intron-containing gene for yeast profiling (PFY) encodes a vital function. Mol Cell Biol 8: 5108–5115.V. MagdolenU. OechsnerG. MullerW. Bandlow1988The intron-containing gene for yeast profiling (PFY) encodes a vital function.Mol Cell Biol851085115
- 120. Haugwitz M, Noegel AA, Karakesisoglou J, Schleicher M (1994) Dictyostelium amoebae that lack G-actin-sequestering profilins show defects in F-actin content, cytokinesis, and development. Cell 79: 303–314.M. HaugwitzAA NoegelJ. KarakesisoglouM. Schleicher1994Dictyostelium amoebae that lack G-actin-sequestering profilins show defects in F-actin content, cytokinesis, and development.Cell79303314
- 121. Verheyen EM, Cooley L (1994) Profilin mutations disrupt multiple actin-dependent processes during Drosophila development. Development 120: 717–728.EM VerheyenL. Cooley1994Profilin mutations disrupt multiple actin-dependent processes during Drosophila development.Development120717728
- 122. Morton BR, Bi IV, McMullen MD, Gaut BS (2006) Variation in mutation dynamics across the maize genome as a function of regional and flanking base composition. Genetics 172: 569–577.BR MortonIV BiMD McMullenBS Gaut2006Variation in mutation dynamics across the maize genome as a function of regional and flanking base composition.Genetics172569577
- 123. Morin PA, Luikart G, Wayne RK, the SNP workshop group (2004) SNPs in ecology, evolution and conservation. Trend Ecol Evol 19: 208–216.PA MorinG. LuikartRK Waynethe SNP workshop group2004SNPs in ecology, evolution and conservation.Trend Ecol Evol19208216
- 124. Barbazuk WB, Emrich SJ, Chen HD, Li L, Schnable PS (2007) SNP discovery via 454 transcriptome sequencing. Plant J 51: 910–918.WB BarbazukSJ EmrichHD ChenL. LiPS Schnable2007SNP discovery via 454 transcriptome sequencing.Plant J51910918
- 125. Kim WJ, Jung HT, Gaffney PM (2011) Development of Type I genetic markers from expressed sequence tags in highly polymorphic species. Mar Biotechnol 13: 127–132.WJ KimHT JungPM Gaffney2011Development of Type I genetic markers from expressed sequence tags in highly polymorphic species.Mar Biotechnol13127132
- 126. Ellis JR, Burke JM (2007) EST-SSRs as a resource for population genetic analyses. Heredity 99: 125–132.JR EllisJM Burke2007EST-SSRs as a resource for population genetic analyses.Heredity99125132
- 127. Gorbach DM, Hu ZL, Du ZQ, Rothschild MF (2010) Mining ESTs to determine the usefulness of SNPs across shrimp species. Anim Biotechnol 21: 100–103.DM GorbachZL HuZQ DuMF Rothschild2010Mining ESTs to determine the usefulness of SNPs across shrimp species.Anim Biotechnol21100103
- 128. Dinh H, Coman G, Hurwood D, Mather P (2011) Experimental assessment of the utility of VIE tags in a stock improvement program for giant freshwater prawn (Macrobrachium rosenbergii) in Vietnam. Aqua Res Published Online. H. DinhG. ComanD. HurwoodP. Mather2011Experimental assessment of the utility of VIE tags in a stock improvement program for giant freshwater prawn (Macrobrachium rosenbergii) in Vietnam.Aqua Res Published OnlineDOI:10.1111/j.1365-2109.2011.02949.x. DOI:10.1111/j.1365-2109.2011.02949.x.
- 129. Chromczynski P, Mackey K (1995) Short technical report. Modification of TRIZOL reagent procedure for isolation of RNA from Polysaccaride-and proteoglycan-rich sources. Biotechniques 19: 942–945.P. ChromczynskiK. Mackey1995Short technical report. Modification of TRIZOL reagent procedure for isolation of RNA from Polysaccaride-and proteoglycan-rich sources.Biotechniques19942945
- 130. Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, et al. (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res 25: 3389–3402.SF AltschulTL MaddenAA SchafferJ. ZhangZ. Zhang1997Gapped BLAST and PSI-BLAST: a new generation of protein database search programs.Nucleic Acids Res2533893402
- 131. Oliveros JC (2007) VENNY: an interactive tool for comparing list with Venn Diagram. VENNY Website. 01: JC Oliveros2007VENNY: an interactive tool for comparing list with Venn Diagram. VENNY Website.01Available: http://bioinfogp.cnb.csic.es/tools/venny/index.html. Accessed 2011 Nov. Available: http://bioinfogp.cnb.csic.es/tools/venny/index.html. Accessed 2011 Nov.
- 132. Gonesa A, Götz S, Garcia-Gomez JM, Terol J, Talon M, et al. (2005) Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research. Bioinformatics 21: 3674–3676.A. GonesaS. GötzJM Garcia-GomezJ. TerolM. Talon2005Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research.Bioinformatics2136743676
- 133. Götz S, Garcia-Gomez JM, Terol J, William TD, Gagaraj SH, et al. (2008) High-throughput functional annotation and data mining with Blast2GO suite. Nucleic Acids Res 36: 3420–3435.S. GötzJM Garcia-GomezJ. TerolTD WilliamSH Gagaraj2008High-throughput functional annotation and data mining with Blast2GO suite.Nucleic Acids Res3634203435
- 134. The Gene Ontology Consortium (2000) Gene Ontology: Tool for the unification of biology. Nat Genetics 25: 25–29.The Gene Ontology Consortium2000Gene Ontology: Tool for the unification of biology.Nat Genetics252529
- 135. The Gene Ontology Consortium (2008) The Gene Ontology project in 2008. Nucleic Acids Res 36: D440–444.The Gene Ontology Consortium 2008The Gene Ontology project in 2008.Nucleic Acids Res36D440444
- 136. Kanehisa M, Goto S, Hattori M, Aoki-Kinoshita KF, Itoh M, et al. (2006) From genomics to chemical genomics: new developments in KEGG. Nucleic Acids Res 34: D354–357.M. KanehisaS. GotoM. HattoriKF Aoki-KinoshitaM. Itoh2006From genomics to chemical genomics: new developments in KEGG.Nucleic Acids Res34D354357
- 137. Kanehisa M, Araki M, Goto S, Hattori M, Hirakawa M, et al. (2008) KEGG for linking genomes to life and the environment. Nucleic Acids Res 35: D480–484.M. KanehisaM. ArakiS. GotoM. HattoriM. Hirakawa2008KEGG for linking genomes to life and the environment.Nucleic Acids Res35D480484
- 138. Hunter S, Apweiler R, Attwood TK, Bairoch A, Bateman A, et al. (2009) InterPro: the integrative protein signature database. Nucleic Acids Res 37: D211–215.S. HunterR. ApweilerTK AttwoodA. BairochA. Bateman2009InterPro: the integrative protein signature database.Nucleic Acids Res37D211215
- 139. Ye J, Zheng H, Zhang Y, Chen J, Zhang Z, et al. (2006) WEGO: a web tool for plotting GO annotations. Nucleic Acids Res 34: W293–297.J. YeH. ZhengY. ZhangJ. ChenZ. Zhang2006WEGO: a web tool for plotting GO annotations.Nucleic Acids Res34W293297
- 140. Meglécz E, Constedoat C, Dubut V, Gilles A, Malausa T, et al. (2010) QDD: a user-friendly program to select microsatellite markers and design primers from large sequencing projects. Bioinfo App Note 26: 403–404.E. MegléczC. ConstedoatV. DubutA. GillesT. Malausa2010QDD: a user-friendly program to select microsatellite markers and design primers from large sequencing projects.Bioinfo App Note26403404
- 141. Rozen S, Skaletsky H (2000) Primer3 in the WWW for general users and for biologist programmers. Methods Mol Biol 132: 365–386.S. RozenH. Skaletsky2000Primer3 in the WWW for general users and for biologist programmers.Methods Mol Biol132365386
- 142. Bekal S, Craig JP, Hudson ME, Niblack TL, Domier LL, et al. (2008) Genomic DNA sequence comparison between two inbred soybean cyst nematode biotypes facilitated by massively parallel 454 micro-bead sequencing. Mol Genet Genomics 279: 535–543.S. BekalJP CraigME HudsonTL NiblackLL Domier2008Genomic DNA sequence comparison between two inbred soybean cyst nematode biotypes facilitated by massively parallel 454 micro-bead sequencing.Mol Genet Genomics279535543