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Restriction site-associated DNA sequencing for SNP discovery and high-density genetic map construction in southern catfish (Silurus meridionalis)

机译:限制性位点相关DNA测序用于南部cat鱼的SNP发现和高密度遗传图谱的构建

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摘要

Single-nucleotide polymorphism (SNP) markers and high-density genetic maps are important resources for marker-assisted selection, mapping of quantitative trait loci (QTLs) and genome structure analysis. Although linkage maps in certain catfish species have been obtained, high-density maps remain unavailable in the economically important southern catfish (Silurus meridionalis). Recently developed restriction site-associated DNA (RAD) markers have proved to be a promising tool for SNP detection and genetic map construction. The objective of the present study was to construct a high-density linkage map using SNPs generated by next-generation RAD sequencing in S. meridionalis for future genetic and genomic studies. An F1 population of 100 individuals was obtained by intraspecific crossing of two wild heterozygous individuals. In total, 77 634 putative high-quality bi-allelic SNPs between the parents were discovered by mapping the parents' paired-end RAD reads onto the reference contigs from both parents, of which 54.7% were transitions and 45.3% were transversions (transition/transversion ratio of 1.2). Finally, 26 714 high-quality RAD markers were grouped into 29 linkage groups by using de novo clustering methods (Stacks). Among these markers, 4514 were linked to the female genetic map, 23 718 to the male map and 6715 effective loci were linked to the integrated map spanning 5918.31 centimorgans (cM), with an average marker interval of 0.89 cM. High-resolution genetic maps are a useful tool for both marker-assisted breeding and various genome investigations in catfish, such as sequence assembly, gene localization, QTL detection and genome structure comparison. Hence, such a high-density linkage map will serve as a valuable resource for comparative genomics and fine-scale QTL mapping in catfish species.
机译:单核苷酸多态性(SNP)标记和高密度遗传图谱是标记辅助选择,定量性状位点(QTL)定位和基因组结构分析的重要资源。尽管已获得某些cat鱼物种的连锁图,但在经济上重要的南部cat鱼(Silurus meridionalis)中仍无法获得高密度图。最近开发的限制性酶切位点相关的DNA(RAD)标记已被证明是用于SNP检测和遗传图谱构建的有前途的工具。本研究的目的是利用子午链球菌中下一代RAD测序产生的SNPs构建高密度连锁图谱,以用于未来的遗传和基因组研究。通过两个野生杂合子个体的种内杂交获得了100个个体的F1种群。通过将父母的配对末端RAD读图映射到父母双方的参考重叠群中,共发现父母之间77 634个高质量的双等位基因SNP,其中54.7%是转化,45.3%是转化(转化/转换率为1.2)。最后,采用从头聚类方法(Stacks)将26×714个优质RAD标记物分为29个连锁群。在这些标记中,4514个与女性遗传图谱相关,23,718与男性图谱相关,6715个有效基因座与跨度5918.31厘摩(cM)的整合图谱相关,平均标记间隔为0.89 cM。高分辨率遗传图谱是marker鱼标记辅助育种和各种基因组研究(例如序列装配,基因定位,QTL检测和基因组结构比较)的有用工具。因此,这种高密度连锁图谱将成为for鱼物种比较基因组学和精细QTL定位的宝贵资源。

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