通过全基因组重测序分析揭示伊朗马种的种群遗传结构。

IF 2.7 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mammalian Genome Pub Date : 2024-06-01 Epub Date: 2024-03-23 DOI:10.1007/s00335-024-10035-6
Babak Arefnejad, Mehrshad Zeinalabedini, Reza Talebi, Mohsen Mardi, Mohammad Reza Ghaffari, Mohammad Farhad Vahidi, Mojtaba Khayam Nekouei, Tomasz Szmatoła, Ghasem Hosseini Salekdeh
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引用次数: 0

摘要

保护遗传多样性对于加强遗传改良和促进对选择的适应性反应至关重要。本研究的重点是识别关键的遗传变异,包括单核苷酸多态性(SNPs)、插入/缺失多态性(INDELs)和拷贝数变异(CNVs),同时探索代表五个本土品种的七匹伊朗马的基因组进化关联性:里海马、土库曼马、达雷舒里马、库尔德马和阿西尔马。通过全基因组重测序,我们获得了 2.7 Gb 的序列数据,原始读数从里海马的 1.2 Gb 到土库曼马的 0.38 Gb 不等。经过过滤后,剩下大约 1.9 Gb 的读数,其中大约 1.5 Gb 成功映射到马参考基因组(EquCab3.0),映射率在 76.4% (里海马)和 98.35% (土库曼马)之间。我们在里海马中发现了 2,909,816 个 SNPs,约占基因组的 0.1%。值得注意的是,这些 SNPs 中的 71% 位于基因间区,8.5% 和 6.8% 分别位于上游和下游。对伊朗马种和非伊朗马种之间 SNPs 的比较分析表明,里海马与土库曼马共享的 SNPs 数量最少。相反,里海马与DareShuri、Quarter、阿拉伯马、标准种马和阿西尔马的遗传关系更为密切。分层聚类突出显示了里海马是一个独特的群组,凸显了其与众不同的基因组特征。里海马表现出独特的遗传特征,其特点是神经系统基因的私人突变丰富,影响感官知觉和意识。这种独特的基因构成形成了交配偏好,标志着一种独立的进化轨迹。此外,生殖基因中的重要非同义单核苷酸多态性(nsSNPs)为管理里海马提供了干预机会。这些发现揭示了伊朗马品种的种群遗传结构,有助于提高马科学在保护、性能特征、气候适应、繁殖和抗病等领域的知识水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unveiling the population genetic structure of Iranian horses breeds by whole-genome resequencing analysis.

Preserving genetic diversity is pivotal for enhancing genetic improvement and facilitating adaptive responses to selection. This study focuses on identifying key genetic variants, including single nucleotide polymorphisms (SNPs), insertion/deletion polymorphisms (INDELs), and copy number variants (CNVs), while exploring the genomic evolutionary connectedness among seven Iranian horses representing five indigenous breeds: Caspian, Turkemen, DareShuri, Kurdish, and Asil. Using whole-genome resequencing, we generated 2.7 Gb of sequence data, with raw reads ranging from 1.2 Gb for Caspian horses to 0.38 Gb for Turkoman horses. Post-filtering, approximately 1.9 Gb of reads remained, with ~ 1.5 Gb successfully mapped to the horse reference genome (EquCab3.0), achieving mapping rates between 76.4% (Caspian) and 98.35% (Turkoman). We identified 2,909,816 SNPs in Caspian horses, constituting around 0.1% of the genome. Notably, 71% of these SNPs were situated in intergenic regions, while 8.5 and 6.8% were located upstream and downstream, respectively. A comparative analysis of SNPs between Iranian and non-Iranian horse breeds showed that Caspian horses had the lowest number of shared SNPs with Turkoman horses. Instead, they showed a closer genetic relationship with DareShuri, Quarter, Arabian, Standardbred, and Asil breeds. Hierarchical clustering highlighted Caspian horses as a distinct cluster, underscoring their distinctive genomic signature. Caspian horses exhibit a unique genetic profile marked by an enrichment of private mutations in neurological genes, influencing sensory perception and awareness. This distinct genetic makeup shapes mating preferences and signifies a separate evolutionary trajectory. Additionally, significant non-synonymous single nucleotide polymorphisms (nsSNPs) in reproductive genes offer intervention opportunities for managing Caspian horses. These findings reveal the population genetic structure of Iranian horse breeds, contributing to the advancement of knowledge in areas such as conservation, performance traits, climate adaptation, reproduction, and resistance to diseases in equine science.

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来源期刊
Mammalian Genome
Mammalian Genome 生物-生化与分子生物学
CiteScore
4.00
自引率
0.00%
发文量
33
审稿时长
6-12 weeks
期刊介绍: Mammalian Genome focuses on the experimental, theoretical and technical aspects of genetics, genomics, epigenetics and systems biology in mouse, human and other mammalian species, with an emphasis on the relationship between genotype and phenotype, elucidation of biological and disease pathways as well as experimental aspects of interventions, therapeutics, and precision medicine. The journal aims to publish high quality original papers that present novel findings in all areas of mammalian genetic research as well as review articles on areas of topical interest. The journal will also feature commentaries and editorials to inform readers of breakthrough discoveries as well as issues of research standards, policies and ethics.
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