Horizontal transfer of genetic material between complex organisms often involves transposable elements (TEs). For example, a DNA transposon mariner has been shown to undergo horizontal transfer between different orders of insects and between different phyla of animals. Here we report the discovery and characterization of an ITmD37D transposon, MJ1, in Anopheles sinensis. We show that some MJ1 elements in Aedes aegypti and An. sinensis contain intact open reading frames and share nearly 99% nucleotide identity over the entire transposon, which is unexpectedly high given that these two genera had diverged 145–200 million years ago. Chromosomal hybridization and TE-display showed that MJ1 copy number is low in An. sinensis. Among 24 mosquito species surveyed, MJ1 is only found in Ae. aegypti and the hyrcanus group of anopheline mosquitoes to which An. sinensis belongs. Phylogenetic analysis is consistent with horizontal transfer and provides the basis for inference of its timing and direction. Although report of horizontal transfer of DNA transposons between higher eukaryotes is accumulating, our analysis is one of a small number of cases in which horizontal transfer of nearly identical TEs among highly divergent species has been thoroughly investigated and strongly supported. Horizontal transfer involving mosquitoes is of particular interest because there are ongoing investigations of the possibility of spreading pathogen-resistant genes into mosquito populations to control malaria and other infectious diseases. The initial indication of horizontal transfer of MJ1 came from comparisons between a 0.4x coverage An. sinensis 454 sequence database and available TEs in mosquito genomes. Therefore we have shown that it is feasible to use low coverage sequencing to systematically uncover horizontal transfer events. Expanding such efforts across a wide range of species will generate novel insights into the relative frequency of horizontal transfer of different TEs and provide the evolutionary context of these lateral transfer events.
Citation: Diao Y, Qi Y, Ma Y, Xia A, Sharakhov I, Chen X, et al. (2011) Next-Generation Sequencing Reveals Recent Horizontal Transfer of a DNA Transposon between Divergent Mosquitoes. PLoS ONE 6(2): e16743. https://doi.org/10.1371/journal.pone.0016743
Editor: James Umen, The Salk Institute, United States of America
Received: September 20, 2010; Accepted: January 12, 2011; Published: February 10, 2011
Copyright: © 2011 Diao 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 work was supported by National Basic Research Program of China (Grant 2007CB513107 to EL) and the US National Institutes of Health (NIH grant AI042121 to ZT). AX and IS are supported by NIH grant R21AI081023. 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.
Horizontal transfer is the transfer of genetic material between reproductively isolated species, which is common among prokaryotes . Horizontal transfer between complex organisms is generally less frequent and often involves transposable elements (TEs) , . Mariner, a DNA transposon originally discovered in Drosophila mauritiana , has been shown to undergo horizontal transfer across different orders of insects and even across different phyla of animals , . More recently, examples of horizontal transfer of DNA transposons have been found in plants  and mammals . DNA transposons are Class II TEs. They usually contain 10–200 bp terminal inverted-repeats (TIRs) which flank one or more open reading frames that encode a transposase. Members of the IS630-Tc1-mariner (ITm) superfamily share a transposase that contains a conserved D(Asp)DE(Glu) or DDD catalytic triad , . The IS630-Tc1-mariner superfamily can be organized in several families including Tc1, mariner, ITmD37E and ITmD37D, which are characterized by unique catalytic motifs of DD34E, DD34D, DD37E, and DD37D, respectively . The numbering, which is conserved within each family, refers to the distance between the second D and the third D or E residues of the catalytic triad.
There are generally three lines of evidence indicating the occurrence of horizontal transfer: high sequence identity between TEs from divergent taxa, incongruence between TE phylogeny and host phylogeny, and patchy distribution of TEs among related host species , . Two types of approaches have been employed to systematically uncover evidence of TE horizontal transfer. PCR survey of diverse organisms followed by sequence and evolutionary analysis has been a productive approach to investigate horizontal transfer of a particular TE of interest , , . More recently, comparative analysis of Drosophila genomes uncovered evidence of potentially new horizontal transfer events and revealed that various groups of TEs showed different propensity to undergo horizontal transfer , . Such whole-genome analysis, when expanded to diverse taxa beyond model organisms, will likely generate novel insights into the relative frequency of horizontal transfer of different TEs and provide the evolutionary context of these lateral transfer events.
Here we report the discovery and characterization of an ITmD37D transposon, MJ1, in an important malaria vector in Asia, Anopheles sinensis. MJ1 elements in Aedes aegypti and An. sinensis share 97% to nearly 99% nucleotide identity over the entire transposon, which is unexpectedly high given that these genera diverged 145–200 million years ago . Phylogenetic analysis of all MJ1 sequences obtained from a survey of 24 mosquito species is consistent with horizontal transfer and leads to hypotheses on the timing and direction of horizontal transfer, which may be tested in the future by expanding the survey of MJ1 sequences. Our analysis is one of a small number of cases in which horizontal transfer of nearly identical TEs among highly divergent species has been thoroughly investigated and strongly supported. We discuss the implications of our finding in light of the ongoing investigations of the possibility of spreading pathogen-resistant genes into mosquito populations to control malaria and other infectious diseases. The initial indication of horizontal transfer of MJ1 came from systematic comparisons between a 0.4x coverage An. sinensis 454 sequence database and available TEs in mosquito genomes. Therefore our success indicate that it is feasible to use low coverage sequencing to move beyond model organisms and systematically uncover new horizontal transfer events. We expect this type of analysis will quickly expand into a diverse range of organisms as sequencing technologies rapidly improve.
Search of a 0.4x coverage An. sinensis sequence database revealed fragments that are nearly identical to an Ae. aegypti MJ1 transposon
BLAST searches were performed on a 0.4x coverage 454 shotgun sequence database of An. sinensis, using a list of 1090 annotated TEs from Ae. aegypti as query ( and tefam.biochem.vt.edu). Aae_MJ1 (TF000904, tefam.biochem.vt.edu) matched eight of the An. sinensis 454 shotgun sequences with 97–99% identity. Considering that Aedes and Anopheles mosquitoes diverged 145–200 million years ago , this level of identity offers a clue for possible horizontal transfer. MJ1 is an ITmD37D DNA transposon and Aae_MJ1 refers to the MJ1 that was first found in the yellow fever mosquito Ae. aegypti . It contains an intact open reading frame with a DD37D catalytic triad , where D stands for aspartic acid. Aae_MJ1 (Aae refers to the genus and species) consists of 9 full-length copies in the genome, three of which share >99% nucleotide identity. The average length of the An. sinensis 454 shotgun sequences is 230 bp and the matches to Aae_MJ1 were 100–300 bp in length. Two of these hits were near the termini of MJ1 and had flanking sequences that were specific to An. sinensis. Of the 1090 elements analyzed during the BLAST searches, Aae_MJ1 is the only element that showed such a high similarity to An. sinensis sequences. The next best match was a Tc1 element (TF000536, 86% identity over a 260-bp fragment), which may result from a more ancient horizontal transfer event and is beyond the scope of the current investigation.
Full-length MJ1 elements in An. sinensis and Ae. aegypti share up to 99% nucleotide identity
Full-length MJ1 sequences were independently obtained in two laboratories from two An. sinensis sources by PCR using the terminal inverted repeat as the primer, which anneal to both ends of MJ1. Nine clones were sequenced and all were confirmed to be An. sinensis MJ1 (Asi_MJ1). These nine clones were nearly identical to each other with some having a 19 nucleotide insertion. As shown in Figure 1, one Asi_MJ1 clone was 99% identical to the Aae_MJ1 consensus over the entire 1.3 kb element. The open reading frames of the two sequences encoded 379 amino acids, which showed >97% identity. Sequences of the Aae_MJ1 consensus and all nine genomic copies in Ae. aegypti are shown in Supplemental File S1 and sequences of the nine Asi_MJ1 clones are included in Supplemental File S2. Deduced peptide sequences of the Aae_MJ1 consensus and all individual MJ1 copies/clones that had intact open reading frames are included in Supplemental File S3. When individual MJ1 copies in Ae. aegypti were compared to individual MJ1 clones in An. sinensis at the nucleotide level, high sequence identities were observed, ranging from 97% to nearly 99%. Similar high identities were also observed at the amino acid level. For example, the Aae_MJ1 in CONTIG_13910, the only Ae. aegypti MJ1 copy that has an intact open reading frame, shares 97% amino acid identity with Asi_MJ1_Clone1. The fact that full-length MJ1 elements from Aedes and Anopheles mosquitoes are highly similar at both nucleotide and the amino acid levels indicates the possibility of horizontal transfer, considering that the two genera had diverged 145–200 million years ago . In comparison, the range of amino acid identities between randomly selected orthologous gene products in Ae. aegypti and An. gambiae was from 28 to 96% with an average of 43% .
A) MJ1 schematic drawn according to the MJ1 consensus from Ae. aegypti. The schematic shows terminal inverted repeats (open arrows at the termini), an open reading frame (black bar with the start and end positions marked), and the relative positions of the catalytic triad, which is comprised of three aspartic acid (D) residues. B) Comparison of MJ1 sequences from Ae. aegypti and An. sinensis. Only variable sites are shown between the Aae_MJ1 consensus and Asi_MJ1_Clone1, a representative of Asi_MJ1 from An. sinensis. A one-base insertion between positions 1246 and 1247 in An. sinensis is not shown. The entire nucleotide sequences are shown in Supplemental Files S1 and S2.
Further confirmation of the presence of MJ1 transposons in An. sinensis
We performed TE-display  to compare and isolate MJ1 insertion sites in individual Ae. aegypti and An. sinensis mosquitoes. There were no shared bands (or shared insertion sites) between Ae. aegypti and An. sinensis while there were multiple shared bands among individuals within each species (Figure 2). We cloned and sequenced a few of these bands recovered from TE-display gels, which further confirmed the presence of MJ1 in both species. More importantly, the recovered insertion site sequences were specific to each species (Figure 2). In other words, sequence flanking the MJ1 insertion site that was recovered from Ae. aegypti matched Ae. aegypti genomic sequence alone. Sequence flanking the MJ1 insertion recovered from An. sinensis matched An. sinensis genomic sequence alone. Using Asi_MJ1 as a probe, we performed in situ hybridization on the polytene chromosomes of An. sinensis. A representative image is shown in Figure 3 and five distinct bands are apparent. These results further confirmed the presence of Asi_MJ1 in An. sinensis. Although it is difficult to determine the exact copy number of MJ1 on the basis of in situ and TE-display results, both experiments suggest that the copy number of MJ1 in An. sinensis is low, most likely less than 10 copies per genome.
A) TE-display showing MJ1 insertion sites in individual Ae. aegypti and An. sinensis mosquitoes. Results from nine individuals of each species are shown. Only part of the TE-display gel is shown. B) and C). Specific MJ1 insertion sites from Ae. aegypti and An. sinensis, respectively. The sequence in the middle is the insertion site sequence recovered from TE-display, which consists of both the MJ1 sequence and the flanking genomic sequence. Sequences flanking MJ1 in Ae. aegypti and An. sinensis only match their respective genomes. Only parts of the sequences are shown.
Arrows point to signals on An. sinensis polytene chromosomes, resulting from hybridization with an Asi_MJ1 probe.
Patchy distribution and dN/dS results are consistent with horizontal transfer of MJ1
A broad survey of MJ1 in 24 species within 5 genera is shown in Table 1. Presence or absence of MJ1 was determined by genomic PCR followed by sequencing. In the case of An. gambiae, An. stephensi, and Cx. quinquefasciatus, the absence of MJ1 was also confirmed by analysis of the genome assembly as well as trace files. MJ1 is restricted to Ae. aegypti and the hyrcanus group of Anopheles mosquitoes, to which An. sinensis belongs. As shown in Table 1, 10 of the 11 species within the hyrcanus group have MJ1 sequences. MJ1 was not found in eight Anopheles species outside the hyrcanus group, including An. lindesayi, a species that belongs to the same subgenus as the hyrcanus group. MJ1 was also not detected in four Culicinae mosquitoes, including Ae. albopictus, a species that is within the same subgenus as Ae. aegypti. All MJ1 copies that were obtained by PCR were confirmed by sequencing and special attention was paid to minimize false positive and false negative results as described in Methods and in Table 1. All MJ1 sequences, the nine genomic copies from Ae. aegypti and the 55 PCR clones from different Anopheles species within the hyrcanus group, are shown in Supplemental Files S1 and S2, respectively. An abbreviated schematic summary of the survey results is also shown in Figure 4, highlighting the fact that MJ1 is restricted to Ae. aegypti and the hyrcanus group of Anopheles mosquitoes. Overall, the pattern of patchy species distribution described in this section coupled with up to 99% sequence identity between MJ1 elements in Aedes and Anopheles mosquito species strongly suggests a recent horizontal transfer event.
Details and a full species list are provided in Table 1. The three species (Anopheles sinensis, Anopheles hyrcanus, and Aedes aegypti) that have MJ1 are highlighted by the horizontal lines. All other species do not have MJ1. The Anopheles and Aedes genera were estimated to have diverged 145–200 million years ago .
It is possible, although not likely, that selection pressure could contribute to the observed 99% conservation of MJ1 sequences between Ae aegypti and An. sinensis. However, analysis of MJ1 copies from Ae. aegypti and the Anopheles species showed dN/dS values ranging from 0.66 to 0.78, with no evidence of strong selection pressure. We have previously calculated dN/dS values for Vg-C, a mosquito gene known to be relatively rapidly evolving . Comparisons of Vg-C genes among Aedes and Anopheles mosquitoes showed dN/dS values ranging from 0.065 to 0.073 . Therefore, the dN/dS values from the MJ1 comparisons suggest that the high sequence identity between the MJ1 elements in Ae. aegypti and An. sinensis does not result from high selection pressure. Taken together, recent horizontal transfer is the only reasonable explanation of the high identity between MJ1 in these highly divergent mosquito species.
Phylogenetic analysis of MJ1 sequences in Ae. aegypti and the hyrcanus group of Anopheles mosquitoes
Phylogenetic relationships of the 64 MJ1 sequences were inferred using a Bayesian program named MrBayes . Shown in Figure 5 is an unrooted phylogeny based on nucleotide sequence alignments (see Supplemental File S4 for the entire alignment and the model and parameters used for phylogenetic reconstruction). The scale bar of the tree is at 0.002 substitutions per site and the variable but overall short branch length of each MJ1 relative to the scale bar reflects the fact that the identity levels among vast majority of these MJ1 sequences are above 97%. All nine copies of the Ae. aegypti MJ1 form a well supported clade (credibility score 1.00) distinct from An. sinensis and other MJ1 sequences, which further argues against contamination being the explanation of the high sequence identity between Ae. aegypti MJ1 and Anopheles MJ1. If midpoint rooting is applied, the nine Ae. aegypti MJ1 sequences form a broader and well supported clade (credibility score 1.00) with two An. peditaeniatus MJ1 (Ape_MJ1_Clone4 and Clone 5) and three An. crawfordi MJ1 (Acr_MJ1_Clone1, Clone 2, and Clone 3). This clade, which is to the right of the midpoint in Figure 5, consists of sequences that appear to be more evolutionary divergent compared to most of the sequences that belong to the clade to the left of the midpoint. For example, the branch length of a MJ1 sequence in the clade to the right of the midpoint is on average longer than the branch length of a MJ1 sequence in the left clade. Moreover, while only one MJ1 (Ae. aegypti Contig_13910) out of the 14 MJ1 in the right clade contains an intact open reading frame for the transposase, 30 of the 50 MJ1 in the left clade contain intact open reading frames (Supplemental Files S3 ). The relationship between most of the MJ1 sequences in the left clade is not well resolved, which is expected given their short branch lengths or high sequence similarities. There are a few cases in which MJ1 from different Anopheles species form a well supported clade (e.g., Ale_MJ1_Clone5 and Aju_MJ1_Clone6; Ale_MJ1_Clone4 and Aju_MJ1_Clone7; Aba_MJ1_Clone3 and Akl_MJ1_Clone1). Such relationships may reflect horizontal transfer or introgression  between these Anopheles species. Note that An. peditaeniatus and An. crawfordi, the two species that contain MJ1 most closely-related to Ae. aegypti MJ1, are the basal lineages within the hyrcanus group , . An. peditaeniatus also contains MJ1 sequences that belong to the clade to the left of the midpoint. It is important to note that all Ae. aegypti MJ1 sequences were obtained from the genome assembly while Anopheles MJ1 were obtained by PCR, which was designed to sample MJ1 sequences with full terminal inverted repeats. The lack of MJ1 in An. kumingensis (Table 1) may reflect a loss of full-length MJ1 because An. kumingensis is among the more derived lineages ,  and all other hyrcanus mosquitoes including its close relative An. kweiyangensis harbor MJ1.
The unrooted phylogeny was inferred from nucleotide sequence alignment of all 64 MJ1 sequences using MrBayes version 3.1.2 . The evolutionary model used during the Bayesian analysis was selected using JModeltest  and 2.5 million generations of analyses were performed to produce the phylogeny and clade credibility scores. Sequence alignment and parameters for phylogenetic analysis are provided in Supplemental File S4 which is an executable Nexus file. Ae. aegypti MJ1 sequences are indicated by their contig names. All other MJ1 sequences are named according to the following convention: The first letter “A” refers to genus Anopheles and the 2nd and 3rd letters are the first two letters of the species name. For example, the first clone of the Anopheles sinensis MJ1 is Asi_MJ1_Clone1. Full species names are shown in Table 1. Ae. aegypti MJ1 and An. sinensis MJ1 are highlighted in blue and red, respectively. Only clades with >0.70 credibility scores are shown as resolved clades. The thickness of the corresponding branches is proportional to the credibility score. Clades with the highest possible credibility value, 1.00, are indicated. Although the tree in this figure is unrooted, the position of midpoint root is indicated.
We uncovered MJ1 transposons in Anopheles mosquitoes and they share up to 99% nucleotide identity with Ae. aegypti MJ1, even though the Aedes and Anopheles genera had diverged 145–200 million years ago. Further analyses of MJ1 insertion sites, species distribution, and selection pressure clearly point to recent horizontal transfer as the only reasonable explanation for such a high identity between MJ1 from these divergent species. It is not reliable to determine the divergence time of these MJ1 sequences on the basis of substitution rates because the number of synonymous substitutions is very low between these highly similar sequences. However, a few observations can be made regarding the evolution of MJ1 on the basis of our phylogenetic analysis. As shown in Figure 5, many Anopheles MJ1 elements may have been recently transposed given the high sequence similarities between clones within and among different species. A few well supported clades consist of MJ1 from different Anopheles species, which may either reflect horizontal transfer or introgression  between these species within the hyrcanus group. Our survey of MJ1 in Anopheles species cannot detect copies that have truncations at any one of the termini and our survey of MJ1 in Aedes has been limited to Ae. aegypti and Ae. albopictus. Nonetheless, here we discuss the timing and direction of the main horizontal transfer event between Aedes and Anopheles mosquitoes, given the current available data and with the understanding that expanded surveys in the future may support different evolutionary scenarios. It is apparent that MJ1 from Ae. aegypti are more closely-related to some of the MJ1 from the two basal species of the hyrcanus group, An. crawfordi and An. peditaeniatus , , than to other Anopheles MJ1 sequences (Figure 5). If we accept midpoint rooting of the unrooted tree shown in Figure 5, Ae. aegypti MJ1 form a well supported clade with some of the MJ1 sequences from the two basal species mentioned above. Thus the most parsimonious interpretation is that MJ1 existed in the common ancestor of the hyrcanus group and the main horizontal transfer event between Aedes and Anopheles may have occurred after the divergence between the basal lineage and the more derived species within the hyrcanus group , . The direction of the horizontal transfer may be from the basal lineage of the hyrcanus group (the clade or subgroup that contains An. crawfordi and An. peditaeniatus) to Aedes. One of the alternative hypotheses, namely transfer of MJ1 from Aedes to the common ancestor of the hyrcanus group, cannot explain the well-supported relationship between Aedes MJ1 and some of the MJ1 elements in An. crawfordi and An. peditaeniatus (Figure 5). The other alternative hypothesis, namely transfer of MJ1 from Aedes to the subgroup that contains An. crawfordi and An. peditaeniatus, cannot explain the existence of MJ1 in the more derived species such as An. sinensis and An. lesteri in the hyrcanus group. To have a better understanding of the timing and direction of the main horizontal transfer event of MJ1 between Aedes and Anopheles mosquitoes, it is important to survey additional mosquito species, especially species that are closely related to Ae. aegypti and to maximize coverage of young and old MJ1 copies in any given species. A better understanding of the phylogenetic relationship and divergence time of species within the Anopheles and Aedes genera will also be helpful to determining the timing and direction of the horizontal transfer of MJ1 between the two genera.
The utility of low-coverage next-generation sequencing has been limited in the absence of a reference genome. However, as shown here, such an approach can readily uncover transposons that exist in multiple copies and identify transposons that may be the subject of very recent horizontal transfer events. In our case, 0.4x coverage was sufficient to identify MJ1, which is a low-copy element in An. sinensis (Figures 2 and 3). We used an earlier version of 454 GS FLX to generate the low-coverage sequences totaling 117 Mbp with an average read length of 230 bp. Currently a single illumina run can provide 1300 Mbp of sequences with 80 bp read length at a cost of $1000 or less. With the implementation of multiplexing and the rapid progress in high-throughput sequencing technology and the continuing reduction of sequencing cost, a broad survey of many species by low-coverage genomic sequencing is within reach and will allow systematic discovery of novel horizontal transfer events. For example, one could obtain low-coverage sequences of a large number of species with ecological overlap to identify repetitive sequences that show unexpectedly high identity between species. Such analysis will lead to candidates of very recent horizontal transfer events, which will likely offer opportunities to investigate the mechanisms and circumstances of horizontal transfer because the factors required for such lateral transfer may still be accessible for examination . Broad low-coverage genomic surveys will also facilitate systematic investigations of the condition and frequency of horizontal transfer events, which has been difficult to study. It is important to note that the role of low-coverage sequencing here is to lead to the discovery of horizontal transfer events, which need to be confirmed by further analysis as shown in this study.
Our discovery also has important practical implications. The existence of MJ1 copies with intact open reading frames in most species and the presence of highly similar copies within and between species suggest that MJ1 may still be active, or an active copy may be constructed. Transformation of mosquitoes has been achieved using exogenous transposons. However, relatively low efficiency and lack of remoblization of these transposons in the mosquito germline hinders genetic manipulations for basic research and for exploring new disease control strategies . MJ1 is a candidate for a new transformation tool that may overcome some of these limitations.
Horizontal transfer has been a long-standing concern associated with a novel strategy to combat mosquito-borne infectious diseases by spreading transgenes that confer resistance to pathogens into mosquito populations . The risk of transfer of an introduced transposon and/or associated transgene to unintended organisms has been difficult to evaluate. The discovery of recent horizontal transfer between mosquito species offers a starting point to investigate the conditions under which horizontal transfer occurs. Future applications of low-coverage next-generation sequencing to a wide range of mosquito species will allow for estimation of the frequency of horizontal transfer events and provide a quantitative basis for risk assessment.
Materials and Methods
454 sequencing of An. sinensis and initial sequence analysis
The Shanghai strain of An. sinensis (National Institute for Parasitic Diseases, Chinese Center for Disease Control and Prevention, Shanghai, China) was used. Genomic DNA was extracted from approximately 500 adult mosquitoes. Subsequent sequencing steps involved in 454 GS FLX sequencing were all performed at the Virginia Bioinformatics Institute at Virginia Tech. Briefly, approximately 10 µg of genomic DNA were fractionated into 300 to 800 bp fragments, to which short adaptors specific for both the 3′ and 5′ ends were added by ligation. The adaptors enable individual genomic DNA fragment to bind a unique bead and get amplified by PCR. The clonally amplified beads, each representing a unique genomic DNA fragment, are used as templates for sequencing. Slightly more than 500,000 sequencing reads passed quality filtering and the average and range of sequence lengths are 230 bp, and 100–300 bp, respectively. A total 117 Mbp (0.4x genome coverage) shotgun sequences were obtained. This shotgun database was formatted for BLASTn analysis on a 2x quad-core Linux server with 32 GB of RAM using all known Ae. aegypti TEs  as query with an e-value cut-off of 1e-5.
Amplification, cloning, and sequencing of MJ1
For confirmation of MJ1 in An. sinensis, we used An. sinensis mosquitoes from two independent sources and carried out subsequent analysis at two different institutions. The first was the Shanghai strain, which was analyzed at the Chinese Academy of Sciences in Shanghai and the second was the Guangdong strain, which was analyzed at Virginia Tech. Adult mosquitoes were homogenized and DNA was extracted by ethanol precipitation and resuspended in 50 µl double-distilled water. Full length MJ1 was obtained using polymerase chain reaction (PCR). PCR was carried out with 1 µl genomic DNA as the template and the Aae_MJ1 terminal inverted repeat as the sole primer (5′-TACACGGTGTTCAATAAGTTC-3′). Either 1 unit of Taq plus or Pfu enzyme was used in a 20 µl reaction. PCR amplification was performed for 30 cycles (50 s denaturation at 94°C, 30 s of annealing at 53°C, and 1.5 min extension at 72°C). PCR products were gel purified, cloned, and multiple clones were sequenced. The same method was used for analysis of other species. As a common practice during all PCR analysis, negative controls with no genomic templates were included and were negative. Additional measures were taken to minimize contamination or false positive results, which included the use of aerosol filter tips during PCR setup, the use of fresh electrophoresis buffer every time when a gel was run, and the use of new cutters for cutting bands every time. All MJ1 copies were confirmed by sequencing and special attention was also paid to minimize false negative results during the species survey. PCR with ITS2 primers was performed as positive controls to confirm genomic DNA integrity. The PCR condition for MJ1 amplification, as described above, allows for amplification of sequences with mismatches to the MJ1 terminal inverted repeat primer. Indeed PCR products from other IS630-Tc1-mariner transposons were sometimes obtained but subsequently determined not to be MJ1 by sequencing.
Fluorescence in situ hybridization
The fourth instars of An. sinensis (Shanghai strain) were preserved in Carnoy's solution (Methanol: Glacial Acetic acid = 3∶1). Polytene chromosomes were prepared from salivary glands. PCR products of an Asi_MJ1 transposon with confirmed sequence were labeled with Cy3 and Cy5-AP3-dUTP (GE Healthcare UK Ltd, Buckinghamshire, England) by Random Primers DNA Labeling System (Invitrogen Corporation, Carlsbad, CA, USA). The DNA probes were hybridized to the chromosomes at 39°C overnight in 2x hybridization buffer (Invitrogen Corporation, Carlsbad, CA, USA). The chromosome preparations were washed in 0.2XSSC, counterstained with YOYO-1, and mounted in DABCO. Under these conditions, the probe would need to be >85% identical to the target to produce a signal. Fluorescent signals were detected and recorded using a Zeiss LSM 510 Laser Scanning Microscope (Carl Zeiss MicroImaging, Inc., Thornwood, NY, USA). Localization of signal was accomplished using a cytogenetic map for An. sinensis .
TE-display and sequencing of DNA recovered from TE-display
TE-display was performed as previously described . Briefly, genomic DNA from individual mosquitoes was digested using BfaI. The digested DNA fragments were ligated to an adapter. Two rounds of PCR were used to amplify the fragments between specific MJ1 sequences and the adapter sequence. A γ-33P labeled nested primer was used in the second round of PCR. The amplified fragments were separated on a sequencing gel. The sequences for the BfaI-adapter were 5′-GACGATGAGTCCTGAG-3′ and 5′-TACTCAGGACTCAT-3′. We used two sets of MJ1-specific primers which gave similar results. The first set of the MJ1-specific primers are: 5′-ACAAACTCCTGACCAGCGTG-3′ and 5′-GATTGAGCGGTTCTTTTTGC-3′. The second set of MJ1-specific primers are: 5′-GATTGAGCGGTTCTTTTTGC-3′ and 5′-CATTGGTCGAGGACGTCTCC-3′. Bands from the TE-display gel were purified, amplified by PCR, cloned, and sequenced.
Computational and phylogenetic analysis
BLAST analysis between different MJ1 sequences was carried out locally on a 2x quad-core Linux server. Multiple sequence alignment was done using Clustalw (http://www.ebi.ac.uk/Tools/clustalw2/, gap opening penalty = 10 and gap extension penalty = 0.05). Consensus was made using CONSENSUS (http://www.hiv.lanl.gov/content/sequence/CONSENSUS/consensus.html). dN/ds analysis was performed using SNAP (www.hiv.lanl.gov) , . Phylogeny of the 64 MJ1 sequences from Ae. aegypti and the hyrcanus group of Anopheles mosquitoes was inferred using MrBayes version 3.1.2  on the nucleotide sequence alignment. Based on the JModeltest  analysis of the alignment, Kimura unequal base frequency model  with rate variation among sites (gamma shape = 2.9370) was selected for MrBayes analysis. Two and a half million generations were run to generate phylogeny and clade credibility scores. Visualization and presentation of the tree is carried out using Figtree (http://tree.bio.ed.ac.uk/software/figtree/). Sequence alignment and parameters for phylogenetic analysis are provided in Supplemental File S4 which is an executable Nexus file.
All 55 Anopheles MJ1 sequences described in this manuscript are submitted to GenBank (accession numbers HQ334205-HQ334259) and are shown in Supplemental File S2.
Nucleotide Sequences of the consensus and the nine copies of MJ1 in Aedes aegypti.
MJ1 sequences from the hyrcanus group of Anopheles mosquitoes.
Peptide sequences of the transposase encoded by Aae_MJ1_CONCENSUS and all individual MJ1 copies that had intact open reading frames.
Alignment of 64 MJ1 sequences and the parameters/model used for phylogenetic analysis.
We thank Dr. L. Zheng at the Institute of Plant Physiology and Ecology, Chinese Academy of Sciences for his guidance and support when the Anopheles sinensis sequencing effort was initiated.
Conceived and designed the experiments: ZJT. Performed the experiments: YD YQ YM AX XC. Analyzed the data: YD YQ YM AX IS JB ZJT. Contributed reagents/materials/analysis tools: YM XC EL. Wrote the paper: ZJT YD YQ IS.
- 1. Lawrence JG (2002) Gene transfer in bacteria: speciation without species? Theor Popul Biol 61: 449–460.
- 2. Keeling PJ, Palmer JD (2008) Horizontal gene transfer in eukaryotic evolution. Nat Rev Genet 9: 605–618.
- 3. Lisch D (2008) A new SPIN on horizontal transfer. Proc Natl Acad Sci U S A 105: 16827–16828.
- 4. Jacobson JW, Medhora MM, Hartl DL (1986) Molecular structure of a somatically unstable transposable element in Drosophila. Proc Natl Acad Sci U S A 83: 8684–8688.
- 5. Robertson HM (1993) The mariner transposable element is widespread in insects. Nature 362: 241–245.
- 6. Robertson HM (1997) Multiple mariner transposons in flatworms and hydras are related to those of insects. J Hered 88: 195–201.
- 7. Diao X, Freeling M, Lisch D (2006) Horizontal transfer of a plant transposon. PLoS Biol 4: e5.
- 8. Pace JK 2nd, Gilbert C, Clark MS, Feschotte C (2008) Repeated horizontal transfer of a DNA transposon in mammals and other tetrapods. Proc Natl Acad Sci U S A 105: 17023–17028.
- 9. Henikoff S (1992) Detection of Caenorhabditis transposon homologs in diverse organisms. New Biol 4: 382–388.
- 10. Shao H, Tu Z (2001) Expanding the diversity of the IS630-Tc1-mariner superfamily: discovery of a unique DD37E transposon and reclassification of the DD37D and DD39D transposons. Genetics 159: 1103–1115.
- 11. Silva JC, Loreto EL, Clark JB (2004) Factors that affect the horizontal transfer of transposable elements. Curr Issues Mol Biol 6: 57–71.
- 12. Biedler JK, Shao H, Tu Z (2007) Evolution and horizontal transfer of a DD37E DNA transposon in mosquitoes. Genetics 177: 2553–2558.
- 13. Handler AM, Zimowska GJ, Armstrong KF (2008) Highly similar piggyBac elements in Bactrocera that share a common lineage with elements in noctuid moths. Insect Mol Biol 17: 387–393.
- 14. Bartolome C, Bello X, Maside X (2009) Widespread evidence for horizontal transfer of transposable elements across Drosophila genomes. Genome Biol 10: R22.
- 15. Loreto EL, Carareto CM, Capy P (2008) Revisiting horizontal transfer of transposable elements in Drosophila. Heredity 100: 545–554.
- 16. Krzywinski J, Grushko OG, Besansky NJ (2006) Analysis of the complete mitochondrial DNA from Anopheles funestus: an improved dipteran mitochondrial genome annotation and a temporal dimension of mosquito evolution. Mol Phylogenet Evol 39: 417–423.
- 17. Nene V, Wortman JR, Lawson D, Haas B, Kodira C, Tu Z, et al. (2007) Genome sequence of Aedes aegypti, a major arbovirus vector. Science 316: 1718–1723.
- 18. Coy MR, Tu Z (2007) Genomic and evolutionary analyses of Tango transposons in Aedes aegypti, Anopheles gambiae and other mosquito species. Insect Mol Biol 16: 411–421.
- 19. Biedler J, Qi Y, Holligan D, della Torre A, Wessler S, et al. (2003) Transposable element (TE) display and rapid detection of TE insertion polymorphism in the Anopheles gambiae species complex. Insect Mol Biol 12: 211–216.
- 20. Ronquist F, Huelsenbeck JP (2003) MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics 19: 1572–1574.
- 21. Joshi D, Choochote W, Min GS (2009) Short report: Natural hybrid between Anopheles kleini and Anopheles sinensis. Am J Trop Med Hyg 81: 1020–1022.
- 22. Hwang UW (2007) Revisited ITS2 phylogeny of Anopheles (Anopheles) Hyrcanus group mosquitoes: reexamination of unidentified and misidentified ITS2 sequences. Parasitol Res 101: 885–894.
- 23. Yajun M, Xu J (2005) The Hyrcanus group of Anopheles (Anopheles) in China (Diptera: Culicidae): species discrimination and phylogenetic relationships inferred by ribosomal DNA internal transcribed spacer 2 sequences. J Med Entomol 42: 610–619.
- 24. O'Brochta DA, Sethuraman N, Wilson R, Hice RH, Pinkerton AC, et al. (2003) Gene vector and transposable element behavior in mosquitoes. J Exp Biol 206: 3823–3834.
- 25. James AA (2005) Gene drive systems in mosquitoes: rules of the road. Trends Parasitol 21: 64–67.
- 26. Ye BH, Li B, Xie C (1983) Further study on saliva gland chromosome of Anopheles sinensis larva. Acta Genetica Sinica 10: 489–492.
Korber B (2000) Computational analysis of HIV molecular sequences. In: Rodrigo AG, Learn GH, editors. HIV Signature and Sequence Variation Analysis. Dordrecht, The Netherlands: Kluwer Academic Publishers. pp. 55–72.
- 28. Nei M, Gojobori T (1986) Simple methods for estimating the numbers of synonymous and nonsynonymous nucleotide substitutions. Mol Biol Evol 3: 418–426.
- 29. Posada D (2009) Selection of models of DNA evolution with JModeltest. Methods Mol Biol 537: 93–112.
- 30. Kimura M (1981) Estimation of evolutionary distances between homologous nucleotide sequences. Proc Natl Acad Sci U S A 78: 454–458.