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Investigation of genetic diversity in the loach Misgurnus anguillicaudatus revealed by whole-genome resequencing

文献类型： 外文期刊

作者： Cui, Xiaojuan 1 ; Deng, Jimin 1 ; Zhang, Yifei 1 ; Han, Ying 1 ; Ou, Mi 2 ; Sun, Yuandong 1 ;

作者机构： 1.Hunan Univ Sci & Technol, Sch Life & Hlth Sci, Xiangtan 411201, Peoples R China

2.Chinese Acad Fishery Sci, Pearl River Fisheries Res Inst, Guangzhou 510380, Peoples R China

关键词： Misgurnus anguillicaudatus; SNP; WGRS; Genetic diversity; DNA fingerprint

期刊名称：BMC GENOMICS （ 影响因子：3.7； 五年影响因子：4.2 ）

ISSN： 1471-2164

年卷期： 2024 年 25 卷 1 期

页码：

收录情况： SCI

摘要： BackgroundThe loach (Misgurnus anguillicaudatus) is a significant freshwater economic fish in China, renowned for its tender meat, delicious taste, and high nutritional value. It is widely distributed across the country, except for the western plateau. However, the loach is currently at risk of population decline and degradation of wildlife resources. Research on genetic diversity provides a crucial foundation for the conservation and development of these fish resources. To enhance the protection and utilization of wild loach germplasm resources, we analyzed the genetic structure and diversity of 60 wild loach populations from Xiangtan City (XT), Shaoyang City (SY), and Yueyang City (XY) in Hunan, Guilin City (GL) and Guiping City (GP) in Guangxi, and Wuhan City (WH) in Hubei. Additionally, we mapped the DNA fingerprints of these 60 wild loaches using 12 high-quality SNP sites.ResultsWhole genome resequencing (WGRS) was conducted on 60 loaches from six regions, yielding a total of 1047.17 Gb of raw data and 1046.98 Gb of clean data. From this 2,812,906 high-quality single nucleotide polymorphisms (SNPs) were identified, of which 10,022 core SNPs were selected to analyze the population genetic structure, and 12 core SNPs were used to assess the genetic diversity and DNA fingerprint. The analysis revealed that the 60 loach samples could be grouped into three clusters: Cluster A comprised the XT, SY, and XY groups; Cluster B included the WH group; and Cluster C consisted of the GL and GP groups. The mean nucleic acid diversity (Pi), heterozygosity (Ho), and expected heterozygosity (He) of SNP markers were 0.130, 0.140, and 0.123, respectively. The average inbreeding coefficient was 0.552, indicating high levels of inbreeding.ConclusionsWhole genome resequencing is an effective high-throughput approach for identifying SNP information in loach germplasm and describing genetic relationships within this genus. DNA fingerprinting based on SNP marker technology can accurately assess the genetic structure and variation within natural loach populations, making it a valuable tool for strain and variation identification. Our findings provide a scientific basis for the conservation, development, and optimal breeding of native loach germplasm resources and contribute to expanding the genetic diversity database of wild loach populations.

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