In non-climacteric fruits, the respiratory increase is absent and no phytohormone is appearing to be critical for their ripening process. They must remain on the parent plant to enable full ripening and be picked at or near the fully ripe stage to obtain the best eating quality. However, huge losses often occur for their quick post-harvest senescence. To understanding the complex mechanism of non-climacteric fruits post-harvest senescence, we constructed two small RNA libraries and one degradome from strawberry fruit stored at 20°C for 0 and 24 h. A total of 88 known and 1224 new candidatemiRNAs, and 103 targets cleaved by 19 known miRNAs families and 55 new candidatemiRNAs were obtained. These targets were associated with development, metabolism, defense response, signaling transduction and transcriptional regulation. Among them, 14 targets, including NAC transcription factor, Auxin response factors (ARF) and Myb transcription factors, cleaved by 6 known miRNA families and 6 predicted candidates, were found to be involved in regulating fruit senescence. The present study provided valuable information for understanding the quick senescence of strawberry fruit, and offered a foundation for studying the miRNA-mediated senescence of non-climacteric fruits.
Citation: Xu X, Yin L, Ying Q, Song H, Xue D, Lai T, et al. (2013) High-Throughput Sequencing and Degradome Analysis Identify miRNAs and Their Targets Involved in Fruit Senescence of Fragaria ananassa. PLoS ONE 8(8): e70959. https://doi.org/10.1371/journal.pone.0070959
Editor: Leonardo Mariño-Ramírez, National Institutes of Health, United States of America
Received: April 29, 2013; Accepted: June 25, 2013; Published: August 19, 2013
Copyright: © 2013 Xu 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 is supported by the National Natural Science Foundation of China (31071836).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.
Fruits are essential component of the human diets, especially from fleshy species, which contain high levels of vitamins, antioxidants and dietary fiber. According to the ripening characteristic, fleshy fruits are designated as climacteric and non-climacteric . Climacteric fruits are characterized by a burst of respiration at the onset of ripening along with a large rise in ethylene production, such as the apple, banana, peach and tomato. They can ripen off the parent plant and get soft and sweet after harvest, and can be picked before the fully ripe stage to maintain quality and extend storage life. Besides, their ripening can be initiated by exposure to exogenous ethylene. In non-climacteric fruits, the respiratory increase is absent and no phytohormone is appearing to be critical for the ripening process, and they can not be initiated by exogenous phytohormone. They must remain on the parent plant to enable full ripening and be picked at or near the fully ripe stage to obtain the best eating quality. However, at ambient temperature, some of the non-climacteric fruits post-harvest senescence occurs very quickly, such as strawberry and cherry, and their storage time is only 2–3 d, which often serious affects fruit quality and marketing value, and causes huge losses. Thus, studies of the complex molecular mechanism of non-climacteric fruits post-harvest senescence and technologies for extending their storage life have attracted considerable attentions.
In recent years, small RNAs (sRNAs) are getting more and more attention for their key roles in post-transcriptional or translational gene regulation –. Small interfering RNAs (siRNAs) and microRNAs (miRNAs) are the two major groups of sRNAs. The miRNAs are short (20 to 24 nucleotides in length), single strand and endogenous non-coding sRNAs molecules that negatively regulate gene expressions at post-transcriptional level identified in nearly all eukaryotes , . The miRNA genes originate in the nucleus, where they are encoded by independent transcriptional units in intergenic regions and transcribed by RNA polymerase II to form pri-miRNA. In plant, the stem loop region of pri-miRNAs are cut by Dicer endonuclease to form small double stranded RNA (dsRNA) miRNA: miRNA* and then transported to cytoplasm by HST , . Then the miRNA* strand is degraded by SDN and the miRNA strand is incorporated in the RNA-induced silencing complex (RISC) with endonuclease AGO , where they serving as a leading RNA to direct cleavage of complementary mRNAs . Recent studies have revealed the key roles of miRNAs in diverse biological processes such as development, hormone response and stresses response –. Several miRNAs also have been found to be effective in regulating different mechanisms entailing plant senescence. For example, miR319 negatively regulates leaf growth and positively regulates leaf senescence by modulating the activity of TCP transcription factors . MiR164 prevents premature overexpression of ORE1, a positive regulator of ageing-induced cell death and senescence, and regulates the senescence and cell death in Arabidopsis thaliana leaves . In the climacteric fruit of tomato, miR156/157 was found to be complementary to the CNR3′ untranslated-region sequence, which was important for MADS-RIN to induce the transcription of ripening-related genes . However, to date, there is no information about the function of miRNAs in non-climacteric fruits post-harvest senescence.
To totally make clear the functions of miRNA on the diverse biological processes, it is essential to exactly identify their target genes and explore their interactions. Recently, the development of degradome sequencing has provided a new method for validation of the splicing targets on a whole genome scale, which has employed in identifying miRNA targets and revolutionized the traditional computational target prediction. It has been successfully applied to screen for miRNA targets in several plants, animal and viruses –. In the present research, to investigate the molecular mechanism of non-climacteric fruits post-harvest senescence, and screen for miRNAs and their targets involved in senescence, two small RNA libraries and one degradome from different storage time strawberry fruit were constructed and sequenced by the high-throughput Illumina Solexa system. A selected number of strawberry fruit miRNAs were then validated by quantitative RT-PCR. Based on these identified miRNAs, we predicted their potential targets by degradome sequencing and analyzed the senescence mechanism for the first time in strawberry fruit.
Analysis of small RNA library data sets
For identification of miRNAs and other endogenous small RNAs involved in senescence of non-respiration climacteric fruit, two independent small RNA libraries from strawberry fruits stored for 0 and 24 h were generated and sequenced by high-throughput Illumina Solexa system. These two small RNA libraries yielded a total of 19,440,558 and 20,983,425 raw reads, respectively (Table 1). After filtering out the adapter sequences as well as sequences with low quality or low-copy, and further removing mRNA, rRNAs, tRNAs, snRNAs, and snoRNAs, a total of 18,759,735 and 20,293,492 mappable small RNA sequences were obtained, respectively (Table 1). The cloning frequency of different sized small RNAs (15–32 nt) was similar between the two libraries. In both libraries, the majority of the sRNAs were 20–24 nt in size, two major peaks at 21 nt and 24 nt were observed (Fig. 1).
Identification of known miRNAs in strawberry fruit
To identify miRNAs involved in senescence in strawberry fruit, all the mappable sRNAs were mapped to the known plant miRNAs in miRbase (19.0) database. A total of 88 known unique mature miRNAs corresponding to 71 pre-miRNAs with high sequence similarity to the known plant miRNAs were identified (Table S1 and Table S2). Most of these known mature miRNAs were 21 nt in length with the remainder being 20 nt or 22 nt long (Table S1 and Table S2), which is similar to the characteristic of miRNAs from other plant species, suggesting that most of the strawberry fruit known miRNAs are processed by DCL 1 . In these identified known miRNAs, there are 72 known mature miRNAs with 60 novel pre-miRNAs were discovered, among them we found 18 pairs of 5p and 3p miRNAs. These pre-miRNAs cannot be mapped to Fragaria vesca genome, but the mature miRNAs can be mapped to the Fragaria vesca genome and the extended sequences at the mapped positions of the genome can potentially form hairpins (Table S1). Moreover, 16 mature miRNAs corresponding to 11 reported pre-miRNAs originating from other plant were identified, which can be mapped to Fragaria vesca genome. Among them, eight 5p or 3p new mature miRNAs corresponding to reported pre-miRNA in miRbase (19.0) were first time detected in this experiment (Table S2). Base on the sequence similarity, these identified 88 known miRNAs could be grouped into 31 miRNA families. Most of these identified miRNA families such as miR156, miR160, miR164 miR166, miR167, miR168, miR169, miR172, miR390, miR395 and miR399 are highly conserved in a variety of plant species (Table S1). In addition, several known but non-conserved miRNA (miR397, miR535, miR828, miR477, miR479, miR3267 and miR7125) that have previously been identified only from a few plant species were also found in our dataset.
Identification of novel miRNAs in strawberry fruit
Confident annotation of novel species-specific miRNAs requires dcl1 or dcl4 knockout mutants , . In the absence of these mutants, the ability of the miRNA flanking sequences to fold-back into a stable hairpin structure is an important criterion for the annotation of new miRNAs . By mapping all unique sRNA sequences to the strawberry genome and predicting the secondary structures of the candidate miRNA precursors, 1157 pre-miRNAs corresponding to 1224 unique mature new candidate miRNAs were first reported in this experiment, of which most were 24 nt in length. These 24 nt length miRNAs were likely to be dependent on DCL3 and the hierarchical action of other DCLs according to the evolution of miRNAs . Among them we found 177 pairs of 5p and 3p new candidate miRNAs. Most of these newly identified miRNAs contained 21–24 nt, and 623 miRNA began with a 5′ uridine (Table S3). The minimum free energy (MFE) of these predicted pre-miRNAs ranged from −14.7 kcal mol−1 to −212.9 kcal mol−1 with an average of −77.23 kcal mol−1, which was similar to the −76.8 kcal mol−1 in Arabidopsis thaliana, −72.4 kcal mol−1 in wheat and −71.0 kcal mol−1 in rice, and was much lower than that of tRNA and rRNA . The minimal free energy index (MFEI) ranged from 0.5 to 2.2 with an average of 1.14 (Table S3), which is obviously higher than other types of RNAs such as tRNAs (0.64), rRNAs (0.59) and mRNAs (0.62–0.66) . These characteristic meet the requirements to maintain the stability of hairpin structure of miRNAs.
Expression profiling of miRNAs in response to senescence
To identify miRNAs involved in senescence in strawberry fruit, the differential expression of miRNAs in the two libraries was analyzed and compared using the counts of reads generated from the high-throughput sequencing. Considering the extremely low abundances might lead to false results, the known and new candidate miRNAs with less than 10 raw reads in the two libraries were removed from the expression analysis. The expression of miRNAs with log2 fold changes higher than 1 was designated as up-regulated, and less than -1 was designated as down-regulated. As showed in Table S5, 158 miRNAs were differentially expressed between the two libraries. Among them, 94 miRNAs were up-regulated and 64 were down-regulated. PC-3p-778131_5, PC-3p-1510675_3, PC-5p-280652_13 and PC-5p-833862_5 had the highest down-regulated fold change. PC-3p-217649_17 had the highest up-regulated fold change in the two libraries. Moreover, some miRNAs both have higher expression and fold changes, such as PC-5p-410_7468, PC-5p-481_6402, PC-5p-1004_3092, gso-miR2109_R+1_1ss14GA, PC-5p-931_3343, mdm-miR395a and PC-3p-8342_429mdm-miR394a were up-regulated, and PC-3p-2227_1439 and gma-miR396a-3p_L+1 were down-regulated (Table 2). There were also most miRNAs with high expression but low log2 fold changes, such as mdm-miR156a_L+1, mdm-miR166e, mdm-miR156b, PC-3p-4_731579, ptc-miR156j_1ss15AT, mdm-miR168b, mdm-miR164e, etc. And among them, mdm-miR156a_L+1 had the highest reads abundant (Table 2). To validate the sequencing results and the expression level of miRNAs that involved in fruit senescence, four new candidate miRNAs and five known miRNAs displaying differential expression pattern in strawberry fruits stored for 0 and 24 h from the high-throughput sequencing were selected for qRT-PCR analysis. Although some of them were identified in low read number by Solexa sequencing, such as PC-5p-306063_12 and zma-MIR167j-p3_1ss14CT, all of them were detected by qRT-PCR and they were quite consistent with the results from sequencing data. Moreover, the high abundance miRNAs, such as PC-3p-2227_1439, PC-5p-481_6402, PC-5p-1004_3092, mdm-miR359a, mdm-miR160a and csi-miR827, were also quite consistent with the results from sequencing data (Fig. 2).
The amount of expression was normalized by the level of actin 7 in qRT-PCR. All reactions of qRT-PCR were repeated three times for each sample. Left indicates the miRNA relative expression generated from the high-throughput sequencing; Right indicates the miRNA relative expression tested by qRT-PCR.
Targets identification for miRNAs by degradome analysis
To further understand the biological function of these identified miRNAs on fruit senescence, the high-throughput degradome sequencing approach was adopted to perform a genome-wide analysis of the mRNAs potentially cleaved by the miRNAs. In total, 8,232,621 raw reads from the strawberry fruits libraries (mixture of strawberry fruit stored for 0 and 24 h) were obtained. After removing the reads without the CAGCAG adaptor, 2,921,958 unique raw reads were mapped to the genome database (http://www.rosaceae.org/projects/strawberry_genome/v1.0/genes/fvesca_v1.0_ genemark_hybrid. fna.gz.). The CleaveLand 3.0 was adopted to identify the sliced targets for the known miRNAs and novel miRNA candidates. As shown in Table S6, the cleavage signature for most of the miRNAs were not detectd in this degradome library, only a total of 103 targets potentially cleaved by 19 known miRNAs families and 55 new candidate miRNAs were identified. Based on the ‘height’ of the degradome peak at each occupied transcript position, these cleaved targets were classified into categories 0, 1, 2, 3 and 4 (Fig. 3), respectively. Category ‘0’ is defined as >1 raw read at the position, abundance at position is equal to the maximum on the transcript, and there is only one maximum on the transcript. Category ‘1’ is defined as >1 raw read at the position, abundance at position is equal to the maximum on the transcript, and there is more than one maximum position on the transcript. Category ‘2’ is defined as >1 raw read at the position, abundance at position is less than the maximum but higher than the median for the transcript. Category ‘3’ is defined as >1 raw read at the position, abundance at position is equal to or less than the median for the transcript. Category ‘4’ is defined as only 1 raw read at the position. Among these identified targets, 30 belonged to category 0, one belonged to category 1, 26 belonged to category 2, 1 belonged to category 3, and 49 belonged to category 4, respectively (Table S6).
T-plots show the distribution of the degradome tags along the full-length of the target mRNA sequence. The red line represents the sliced target transcripts. (A) Example of the category 0 target gene03956−v1.0−hybrid for mdm−miR171a. (B) Example of the category 1 target gene07624−v1.0−hybrid for mtr−MIR1510a−p3_1ss5AT. (C) Example of the category 2 target gene05900−v1.0−hybrid for mdm−miR396b. (D) Example of the category 3 target gene18113−v1.0−hybrid for PC−5p−150653_24. (E) Example of the category 4 target gene04565−v1.0−hybrid for mdm−miR156b and gene01896−v1.0−hybrid for PC−5p−15285_237. The categories were based on the relative abundance of the tags at the target sites.
Based on the BLASTX analysis, 51.5% of the identified miRNA targets detectd in this degradome library were homologous to the genes that have already been found in A. thaliana and Oryza sativa (Table S6). Some of these genes have been found to be involved in plant senescence, such as auxin response factor, NAC domain transcriptional regulator superfamily protein, growth-regulating factor, alpha/beta-hydrolases superfamily protein, hydroxy methylglutaryl CoA reductase, Myb protein, Pectin lyase-like superfamily protein, Acyl-CoA N-acyltransferases (NAT) superfamily protein, glycosyl hydrolase and beta-galactosidase (Table 3). Moreover, target genes such as trehalose-phosphatase, ARM repeat superfamily protein, disease resistance protein, calmodulin-binding protein and ABA-induced PP2C gene were also identified in the degradome library, which have been reported to be involved in plant stress response.
GO function analysis of targets
To better understand the function of the identified miRNA and reveal the miRNA-gene regulatory network, the target genes obtained from degradome library were subjected to Gene Ontology (GO) analysis based on the A. thaliana and O. sativa databases. The results of GO analysis showed that the molecular functions of 53 identified targets were involved in DNA or RNA binding, hydrolase activity, protein binding, ATP binding, nucleic acid binding, DNA binding transcription factor activity, catalytic activity, nucleotide binding, transferase activity, kinase activity, other enzyme activity and other molecular function (Fig. 4A). These targets participated in many biological processes, including developmental process, cellular process, biosynthetic process, regulation of transcription, metabolic process, response abiotic and biotic stimulus, anatomical structure morphogenesis, reproduction, carbohydrate metabolic process, transport, cellular protein modification process, response to stress, cell differentiation, cellular component organization, catabolic process, signal transduction, lipid metabolic process and other biological process (Fig. 4B). In addition, the molecular function and biological processes of 50 targets were still unknown.
Strawberry fruit is worldwide appreciated for its unique flavour and high levels of vitamins, antioxidants, dietary fiber, flavonoids, manganese, folate, potassium and ellargic acid (a cancer reduction agent). As the non-climacteric fruit, it must be picked at or near the fully ripe stage to obtain the best eating quality, and huge losses often occur for its rapid post-harvest senescence. Hence, study the mechanisms of strawberry fruit senescence has practical and basic importance. Up to date, many plant miRNAs have been identified and deposited to miRBase, and some of their biological functions also have been studied. To understand the roles of miRNAs in regulation strawberry fruit senescence, two libraries from strawberry fruit stored at 20°C for 0 and 24 h were constructed. Using high-throughput deep sequencing technology, we pyrosequenced sRNA populations at the genome-wide level, and a much wide range of sRNAs with 15–32 nt in length were identified (Fig. 1). According to the analysis from miRBase 19.0, 88 known miRNAs and 1244 new candidate miRNAs were sequenced in the two libraries. By the degradome sequencing approach, we for the first time identified 103 targets, and 53 were homologous to the genes that have already been found in A. thaliana and O. sativa (Table S6). Most of these homologous genes have already been found to be involved in plant development, stress response, signal transduction, kinase activity and metabolic processes. Fortunately, 17 targets identified in the degradome were found to be related to plant senescence (Table 3).
In Arabidopsis leaves, NAC [No apical meristem (NAM), Arabidopsis transcription activation factor (ATAF), Cup-shaped cotyledon (CUC)] transcription factor ORE1 (ORESARA1, oresara means ‘long living’ in Korean), the positive regulator of ageing-induced cell death and senescence, is negative regulated by miR164. During leaf ageing, miR164 progressively decreases and ORE1 expression increases . In the present study, 3 members of the miR164 family, mdm-miR164d_1ss21AC, mdm-miR164e and ptc-miR164f_1ss21TA were identified in the strawberry fruit (Table S4). Their targets were obtained in the degradome library and annotated as NAC domain transcriptional regulator superfamily protein, NAC domain containing protein 87 and NAC domain containing protein 38 (Table 3). In the process of strawberry fruit senescence from 0 h to 24 h, the reads of mdm-miR164e decreased from 53,961 to 44,505, the reads of mdm-miR164d_1ss21AC decreased from 418 to 406, and the ptc-miR164f_1ss21TA reads increased from 30 to 50 (Table S5). Though there were no significant changes of the log2 fold, the significant decrease of mdm-miR164e expression could enhance the expression of NAC domain transcriptional regulator superfamily protein, NAC domain containing protein 87 or NAC domain containing protein 38, and by which they might positively regulate cell death and senescence, and lead to rapid post-harvest senescence of strawberry fruit.
Auxin response factors (ARF) are transcription factors that bind with specificity to TGTCTC auxin response elements (AuxRE) in promoters of auxin response genes and regulate their expression , . In Arabidopsis leaves, it has been reported that ARF2, 7, and 19 transcripts increased moderately, and ARF1 transcripts decreased slightly in response to dark induced senescence . arf2 single mutants also can delay leaf senescence, and in arf1 arf2 double mutants, this phenotype is enhanced . ARF6 and 8 have been reported to be targets of miR167, function in promoting both stamen and gynoecium maturation by increasing jasmonic acid (JA) production, and controlling adventitious root initiation by regulating JA homeostasis . ARF10, 16, and 17 are targets of miR160 . In our results, mdm-miR160a,e and mdm-miR167b_R+1_1ss21AC were also identified, and their targets were ARF 16 and 8, respectively (Table 3). In the process of fruit senescence, the reads of mdm-miR160a and mdm-miR160e increased from 45 to 70, respectively. In contrast, the reads of mdm-miR167b_R+1_1ss21AC significantly decreased from 33,933 to 26,538 (Table S5). The significant decrease of mdm-miR167b_R+1_1ss21AC expression could increase high expression of ARF8, and the increase of mdm-miR160a,e expression could decrease the expression of ARF 16. Considering the important roles of ARF8 in regulating the production of JA, it must have involved in fruit senescence. The ARF16 whether has involved in post-harvest senescence of strawberry fruit, is worthy of our further research.
Myb transcription factors play key roles in regulating diverse transcriptional events in all eukaryotes. BMyb, the ubiquitously expressed member of Myb gene family, has been reported to be effect in rescuing senescence induced by an activated ras oncogene in rodent cells in vitro . Overexpression of DMyb in the imaginal discs of Drosophila led to increased levels of apoptosis , . Studies on vertebrate Myb family proteins in apoptosis also demonstrated their roles in both pro- and anti-apoptotic , . In the present research, the target of Myb protein 1 was identified, which was regulated at different cleavage site by two new candidate miRNA, PC-3p-140510_25 and PC-3p-140510_25, respectively. In the process of fruit senescence, the reads of PC-3p-140510_25 decreased from 47 to 30 (Table S5). We hypothesized that the decrease of PC-3p-140510_25 may play a role in increasing the expression of Myb and promoting senescence in strawberry fruit.
Three hydrolases and 1 lyase were also identified in the degradome library. They were alpha/beta-Hydrolases superfamily protein, beta-galactosidase 3, glycosyl hydrolase 9B1 and Pectin lyase-like superfamily protein, and were regulated by aly-miR169k-3p_L+1, PC-5p-67794_53, hbr-MIR2118-p3_1ss1GT, PC-5p-1004_3092 and PC-3p-87823_40, respectively(Table 3). In the process of strawberry fruit senescence from 0 h to 24 h, the reads of PC-5p-1004_3092 increased from 206 to 1943, and the reads of aly-miR169k-3p_L+1 decreased from 45 to 30 (Table S5). Nevertheless, the reads of PC-5p-67794_53, hbr-MIR2118-p3_1ss1GT and PC-3p-87823_40 showed no significant changes (Table S5). In plants, cell wall plays important role in controlling the cell size and shape. It is also the first obstacle that a pathogen needs to overcome in order to penetrate the plant cell. Its structure is complex and contains various components such as polysaccharides, lignin and proteins. Glycoside hydrolases are common enzymes across all domains of life. They are involved in the metabolism of various carbohydrates containing compounds present in the plant tissues and the degradation and reorganization of cell wall polysaccharides, thereby acting to control fruit softening during ripening . The high level expression of PC-5p-1004_3092 decreased the transcriptions of glycosyl hydrolase 9B1 and might disturb the appropriate balance between degradation and reorganization of cell wall polysaccharides, which probably also related to the quick senescence of strawberry fruit.
Moreover, two senescence relative genes, hydroxy methylglutaryl CoA reductase 1 (HMGR1) and Acyl-CoA N-acyltransferases (NAT) superfamily protein, were identified in the present study, and they were targeted by mdm-miR535d_1ss7CT and PC-3p-269545_14, respectively (Table 3). In the process of strawberry fruit senescence from 0 h to 24 h, the reads of mdm-miR535d_1ss7CT decreased from 28,072 to 23,491, and the reads of PC-3p-269545_14 increased from 10 to 12 (Table S5). In the typical climacteric fruit of tomato, two peaks of HMGR mRNA accumulation were observed during early development and ripening, and HMGR1 and HMGR2 is responsible for the early development peak correlated with high cell division activity and the ripening-associated peak, respectively –. The melon, another climacteric fruit, which only contains a single HGMR gene, also has two-peak expression pattern of HMGR gene during fruit development and ripening , indicated that HMGR was involved in the fruit development, ripening and senescence. In the present study, significant decrease of mdm-miR535d_1ss7CT increased the expression of HMGR1, which maybe another mechanism that related to the quick senescence of strawberry fruit.
In summary, for the first time, we obtained a total of 88 known and 1224 new candidate miRNAs from the senescence of strawberry fruit, and identified 103 targets cleaved by 19 known miRNAs families and 55 new candidate miRNAs. Among them, 14 targets cleaved by 6 known miRNA families and 6 new candidate were involved in fruit senescence. These findings provided valuable information for understanding the quick senescence of strawberry fruit and even non-climacteric fruits, and also offered a foundation for future studies of the miRNA-mediated fruit senescence.
Materials and Methods
Strawberry fruit material
Strawberry (Fragaria ananassa L. cv. Zhangji) fruits were harvested at commercial maturity from an orchard (a private orchard, the owner of Ms. Ma have given permission to conduct the study on this site) in the Xiasha district, Hangzhou, China, and transported to laboratory immediately where they were sorted based on size without physical injuries or infections. The fruits were put in trays with plastic bag to maintain a relative humidity (about 85%), then stored at 20°C for 0, 24, 48 h. No specific permissions were required for these locations/activities, and this study was supported by the National Natural Science Foundation of China (31071836). We confirm that this study did not involve endangered or protected species.
Total RNA isolation, small RNA library construction and sequencing
The fruits stored at 20°C for 0 and 24 h (the fruit stored for 48 h showed excessive senescence) were collected and frozen in liquid nitrogen immediately, and then stored at −80°C, respectively. Total RNA was extracted using mirVana miRNA Isolation Kit (Ambion, Austin, TX, USA) according to the manufacturer's instructions. Subsequently, equal quantities (10 mg) of small RNA were used for sequencing by the Genome Analyzer GA-I (Illumina, San Diego, USA) following the vendor's instructions.
Analysis of sequencing data
The small RNA sequences were processed using Illumina's Genome Analyzer Pipeline software to filter out the 5′ and 3′ adapter sequences, and low quantity reads, and then subjected to a series of data filtration steps to obtain mappable sequences using ACGT101-miR v4.2 (LC Sciences, TX, USA). After removed the mRNA and Rfam (rRNA, tRNA, snRNA, snoRNA and repeat sequence), all the trimmed sequences between 15 and 32 bp in length were mapped to miRNA sequences from the miRNA database, miRbase 19.0 (http:// www.mirbase.org/).
To identify potential miRNA precursor sequences, all identified strawberry fruit mature miRNA sequences were BLASTed against the strawberry genome sequences which downloaded from database (http://www.rosaceae.org/). Secondary structure prediction of miRNA precursor was performed by UNAfold software (http://rna.tbi.univie.ac.at/cgi-bin/RNAfold.cgi). In addition, the rest unmapped small RNA sequences were also BLASTed against the strawberry genome sequences and the secondary structure were predicted as above. The non-coding sequences which could form a perfect stem-loop structure and meet the standard of miRNAs prediction  were regarded as novel miRNA candidates.
Verification of strawberry fruit miRNAs by quantitative realtime PCR (qRT-PCR)
To validate the levels of miRNAs, the expression of 8 selected miRNAs were determined by qRT-PCR with SYBR Premix Ex Taq TM II (TaKaRa, Dalian, China) on the iCycler iQ real-time PCR detection system (Bio-Rad). The specific forward primers of 8 selected miRNAs were designed according to the sequence of miRNA itself (Table S7). Total RNA was extracted from the F. ananassa fruit stored at 20°C for 0 and 24 h with TRIZOL reagent following the manufacturer's instructions (Invitrogen). Then the total RNA (1 μg) was treated with DNase I and reverse-transcribed according to the manufacturer's protocol (Transgene, Beijing, China). The relative expression level of miRNA was calculated according to the method of Livak and Schmittgen .
Degradome library construction and target identification
To investigate the potential target mRNAs involved in fruit senescence, a degradome library was constructed from strawberry fruit (mixture of strawberry fruit stored for 0 and 24 h) according to the methods of German et al. , . In brief, 1 mg of polyA-enriched RNA was ligated to a 5′ RNA oligonucleotide adaptor which containing a 3′ MmeI recognition site. The first strand cDNA was synthesized by reverse transcription (RT) using the ligated products. Then a short PCR (five cycles) was employed to amplify the cDNA to obtain sufficient quantities of DNA products. After digestion with MmeI and purification with PAGE-gel, the PCR product was ligated to 39-double strand DNA adaptor, and then PAGE-gel purified again for PCR (21 cycles). The final cDNA library was purified and sequenced with a Solaxa/Illumina genome analyzer (LC Sciences, Hangzhou, China). A Public software package, CleaveLand3.0 was used for analyzing sequencing data , .
Profile of known microRNAs originating from pre-miRNAs that cannot be mapped to Fragaria vesca genome, but the microRNAs were mapped to the genome and the extended sequences at the mapped positions of the genome potentially form hairpins.
Profile of known microRNAs originating from other plant pre-miRNAs(miRbase 19.0) that can be mapped to Fragaria vesca Genome.
Profile of new candidate microRNAs originating from predicted RNA hairpins.
Profiles of all the microRNAs discovered in this experiment.
Expression profiling of miRNAs in strawberry fruit stored at 20°C for 0 and 24 h.
Information of miRNA targets by degradome sequencing and GO function analysis.
We thank Ms. Ma for providing the Strawberry fruits. We thank Dr. QL Lang and CZ Jin from LC-Bio for small RNA-seq and data analysis.
Conceived and designed the experiments: XX HS BS HW XS. Performed the experiments: XX LY QY TL. Analyzed the data: XX HS. Contributed reagents/materials/analysis tools: DX MX. Wrote the paper: XX HS.
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