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Genome-Wide SNP Discovery from Transcriptome of Four Common Carp Strains

文献类型： 外文期刊

作者： Xu, Jian 1 ; Ji, Peifeng 1 ; Zhao, Zixia 1 ; Zhang, Yan 1 ; Feng, Jianxin 3 ; Wang, Jian 1 ; Li, Jiongtang 1 ; Zhang, Xia 1 ;

作者机构： 1.Chinese Acad Fishery Sci, Ctr Appl Aquat Genom, Beijing, Peoples R China

2.Chinese Acad Fishery Sci, Heilongjiang Fisheries Res Inst, Harbin, Peoples R China

3.Henan Acad Fishery Sci, Zhengzhou, Henan, Peoples R China

4.Natl Fish Hatchery Xingguo Red Carp, Xingguo, Jiangxi, Peoples R China

期刊名称：PLOS ONE （ 影响因子：3.24； 五年影响因子：3.788 ）

ISSN： 1932-6203

年卷期： 2012 年 7 卷 10 期

页码：

收录情况： SCI

摘要： Background: Single nucleotide polymorphisms (SNPs) have been used as genetic marker for genome-wide association studies in many species. Gene-associated SNPs could offer sufficient coverage in trait related research and further more could themselves be causative SNPs for traits. Common carp (Cyprinus carpio) is one of the most important aquaculture species in the world accounting for nearly 14% of freshwater aquaculture production. There are various strains of common carp with different economic traits, however, the genetic mechanism underlying the different traits have not been elucidated yet. In this project, we identified a large number of gene-associated SNPs from four strains of common carp using next-generation sequencing. Results: Transcriptome sequencing of four strains of common carp (mirror carp, purse red carp, Xingguo red carp, Yellow River carp) was performed with Solexa HiSeq2000 platform. De novo assembled transcriptome was used as reference for alignments, and SNP calling was done through BWA and SAMtools. A total of 712,042 Intra-strain SNPs were discovered in four strains, of which 483,276 SNPs for mirror carp, 486,629 SNPs for purse red carp, 478,028 SNPs for Xingguo red carp and 488,281 SNPs for Yellow River carp were discovered, respectively. Besides, 53,893 inter-SNPs were identified. Strain-specific SNPs of four strains were 53,938, 53,866, 48,701, 40,131 in mirror carp, purse red carp, Xingguo red carp and Yellow River carp, respectively. GO and KEGG pathway analysis were done to reveal strain-specific genes affected by strain-specific non-synonymous SNPs. Validation of selected SNPs revealed that 48% percent of SNPs (12 of 25) were tested to be true SNPs. Conclusions: Transcriptome analysis of common carp using RNA-Seq is a cost-effective way of generating numerous reads for SNP discovery. After validation of identified SNPs, these data will provide a solid base for SNP array designing and genome-wide association studies.

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