Xiao Shijun, Han Zhaofang, Wang Panpan, Han Fang, Liu Yang, Li Jiongtang, Wang Zhi Yong
Key Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture; Fisheries College, Jimei University, Xiamen, Fujian, China.
Chinese Academy of Fishery Sciences, Beijing, China.
PLoS One. 2015 Apr 24;10(4):e0124432. doi: 10.1371/journal.pone.0124432. eCollection 2015.
Large yellow croaker (Larimichthys crocea) is an important economic fish in China and Eastern Asia. Because of the exhaustive fishing and overdense aquaculture, the wild population and the mariculture of the species are facing serious challenges on germplasm degeneration and susceptibility to infectious disease agents. However, a comprehensive transcriptome from multi-tissues of the species has not been reported and functional molecular markers have not yet been detected and analyzed. In this work, we applied RNA-seq with the Illumina Hiseq2000 platform for a multi-tissue sample of large yellow croaker and assembled the transcriptome into 88,103 transcripts. Of them, 52,782 transcripts have been successfully annotated by nt/nr, InterPro, GO and KEGG database. Comparing with public fish proteins, we have found that 34,576 protein coding transcripts are shared in large yellow croaker with zebrafish, medaka, pufferfish, and stickleback. For functional markers, we have discovered 1,276 polymorphic SSRs and 261, 000 SNPs. The functional impact analysis of SNPs showed that the majority (~75%) of small variants cause synonymous mutations in proteins, followed by variations in 3' UTR region. The functional enrichment analysis illuminated that transcripts involved in DNA bindings, enzyme activities, and signal pathways prominently exhibit less single-nucleotide variants but genes for the constituent of the muscular tissue, the cytoskeleton, and the immunity system contain more frequent SNP mutations, which may reflect the structural and functional selections of the translated proteins. This is the first work for the high-throughput detection and analysis of functional polymorphic SSR and SNP markers in a comprehensive transcriptome of large yellow croaker. Our study provides valuable transcript sequence and functional marker resources for the quantitative trait locus (QTL) identification and molecular selection of the species in the research community.
大黄鱼(Larimichthys crocea)是中国和东亚地区重要的经济鱼类。由于过度捕捞和高密度养殖,该物种的野生种群和海水养殖面临着种质退化和易感染病原体的严峻挑战。然而,尚未有关于该物种多组织的综合转录组报道,也未检测和分析功能分子标记。在本研究中,我们利用Illumina Hiseq2000平台对大黄鱼的多组织样本进行RNA测序,并将转录组组装成88,103个转录本。其中,52,782个转录本已通过nt/nr、InterPro、GO和KEGG数据库成功注释。与公共鱼类蛋白质进行比较,我们发现大黄鱼与斑马鱼、青鳉、河豚和棘鱼共享34,576个蛋白质编码转录本。对于功能标记,我们发现了1,276个多态性SSR和261,000个SNP。SNP的功能影响分析表明,大多数小变异(约75%)在蛋白质中引起同义突变,其次是3'UTR区域的变异。功能富集分析表明,参与DNA结合、酶活性和信号通路的转录本显著表现出较少的单核苷酸变异,但肌肉组织、细胞骨架和免疫系统组成成分的基因含有更频繁的SNP突变,这可能反映了翻译后蛋白质的结构和功能选择。这是首次对大黄鱼综合转录组中的功能多态性SSR和SNP标记进行高通量检测和分析的工作。我们的研究为该物种在研究群体中的数量性状位点(QTL)鉴定和分子选择提供了有价值的转录序列和功能标记资源。