首页> 外文期刊>BMC Genomics >A ddRAD-based genetic map and its integration with the genome assembly of Japanese eel (Anguilla japonica) provides insights into genome evolution after the teleost-specific genome duplication
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A ddRAD-based genetic map and its integration with the genome assembly of Japanese eel (Anguilla japonica) provides insights into genome evolution after the teleost-specific genome duplication

机译:基于ddRAD的遗传图谱及其与日本鳗(Anguilla japonica)基因组装配的集成为硬骨鱼特异性基因组复制后的基因组进化提供了见解

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Background Recent advancements in next-generation sequencing technology have enabled cost-effective sequencing of whole or partial genomes, permitting the discovery and characterization of molecular polymorphisms. Double-digest restriction-site associated DNA sequencing (ddRAD-seq) is a powerful and inexpensive approach to developing numerous single nucleotide polymorphism (SNP) markers and constructing a high-density genetic map. To enrich genomic resources for Japanese eel (Anguilla japonica), we constructed a ddRAD-based genetic map using an Ion Torrent Personal Genome Machine and anchored scaffolds of the current genome assembly to 19 linkage groups of the Japanese eel. Furthermore, we compared the Japanese eel genome with genomes of model fishes to infer the history of genome evolution after the teleost-specific genome duplication. Results We generated the ddRAD-based linkage map of the Japanese eel, where the maps for female and male spanned 1748.8?cM and 1294.5?cM, respectively, and were arranged into 19 linkage groups. A total of 2,672 SNP markers and 115 Simple Sequence Repeat markers provide anchor points to 1,252 scaffolds covering 151?Mb (13%) of the current genome assembly of the Japanese eel. Comparisons among the Japanese eel, medaka, zebrafish and spotted gar genomes showed highly conserved synteny among teleosts and revealed part of the eight major chromosomal rearrangement events that occurred soon after the teleost-specific genome duplication. Conclusions The ddRAD-seq approach combined with the Ion Torrent Personal Genome Machine sequencing allowed us to conduct efficient and flexible SNP genotyping. The integration of the genetic map and the assembled sequence provides a valuable resource for fine mapping and positional cloning of quantitative trait loci associated with economically important traits and for investigating comparative genomics of the Japanese eel.
机译:背景技术下一代测序技术的最新进展已实现了对整个或部分基因组进行具有成本效益的测序,从而允许发现和表征分子多态性。双消化限制性位点相关的DNA测序(ddRAD-seq)是一种功能强大且便宜的方法,可用于开发众多单核苷酸多态性(SNP)标记并构建高密度遗传图谱。为了丰富日本鳗(Anguilla japonica)的基因组资源,我们使用离子洪流型个人基因组机和将当前基因组装配的支架锚定到日本鳗的19个连接基团上,构建了基于ddRAD的遗传图。此外,我们将日本鳗鱼基因组与模型鱼类的基因组进行了比较,以推断硬骨鱼特异性基因组复制后的基因组进化历史。结果我们生成了基于ddRAD的日本鳗鱼连锁图,其中雌性和雄性图分别跨越1748.8?cM和1294.5?cM,并被分为19个连锁组。总共2,672个SNP标记和115个简单序列重复标记为覆盖日本鳗鱼当前基因组的151?Mb(13%)的1,252个支架提供了锚定点。对日本鳗鱼,,斑马鱼和斑点基因组进行的比较显示,硬骨鱼之间的保守性很高,并揭示了硬骨鱼特异性基因组重复后不久发生的八种主要染色体重排事件的一部分。结论ddRAD-seq方法与离子激流个人基因组机测序相结合,使我们能够进行有效而灵活的SNP基因分型。遗传图谱和组装序列的整合,为与经济重要性状相关的数量性状基因座的精细定位和位置克隆以及调查日本鳗的比较基因组学提供了宝贵的资源。

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