基于高密度snp的短头Luciobarbus生长相关性状全基因组重测序图谱构建及QTL分析

IF 2.8 3区 生物学 Q2 GENETICS & HEREDITY
Frontiers in Genetics Pub Date : 2025-08-18 eCollection Date: 2025-01-01 DOI:10.3389/fgene.2025.1644874
Xuanpeng Wang, Dandan Gao, Gaowei Zhang, Yongchun Ge, Xinhai Wang
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引用次数: 0

摘要

简介:短头Luciobarbus brachycephalus(俗称咸鱼)是中国一种具有商业价值的鱼类,对区域水产养殖经济做出了重大贡献。高密度遗传连锁定位与数量性状位点(QTL)分析相结合已成为阐明水生物种复杂性状遗传机制的有力手段。方法:本研究旨在通过全基因组重测序策略,构建基于snp的高密度连锁图谱,利用父本、母本和165个F1全同胞后代,对6个经济上重要的生长相关性状进行全面的QTL定位,以确定短头l生长调控的候选基因。结果:Pearson相关分析显示,6个生长相关性状之间存在较强的相关性(r < 0.05, P < 0.001),表明可能通过共享遗传因子进行多效性调控。brachycephalus的高密度连锁图谱包含164,435个高质量snp,分布在50个连锁群中,实现了6,425.95 cM的全基因组覆盖。异常的标记密度(平均标记间距离= 0.10 cM)使其成为迄今为止报道的该物种最精确的遗传图谱,从而实现准确的候选基因定位和增强的标记辅助选择。通过QTL定位分析,基于全基因组优势值的峰值对数,确定了几个与生长相关性状显著相关的基因组区域。具体来说,身高的一个主要QTL位于连锁群(LG27)上,体重的两个不同QTL位于l20和LG26上。值得注意的是,在LG27上发现4个纵向生长性状(全长、体长、叉长和肛前体长)在相同的显著QTL区间内共定位。这些QTL区间所鉴定的表型方差占各性状表型方差的6.27 ~ 39.36%。此外,通过对这些显著QTL区间的综合分析,确定了可能调控每个目标性状的候选基因。讨论:这种综合方法为标记辅助选择提供了基础,并增强了对这一重要物种生长相关遗传机制的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High-density SNP-based linkage map construction and QTL analysis for growth-related traits in <i>Luciobarbus brachycephalus</i> using whole-genome resequencing data.

High-density SNP-based linkage map construction and QTL analysis for growth-related traits in <i>Luciobarbus brachycephalus</i> using whole-genome resequencing data.

High-density SNP-based linkage map construction and QTL analysis for growth-related traits in <i>Luciobarbus brachycephalus</i> using whole-genome resequencing data.

High-density SNP-based linkage map construction and QTL analysis for growth-related traits in Luciobarbus brachycephalus using whole-genome resequencing data.

Introduction: Luciobarbus brachycephalus (commonly known as the Aral barbel) represents a commercially valuable fish species in China, contributing significantly to regional aquaculture economies. High-density genetic linkage mapping coupled with quantitative trait locus (QTL) analysis has emerged as a powerful approach for elucidating the genetic mechanism of complex traits in aquatic species.

Method: The present study aimed to construct a SNP-based high-density linkage map using male parent, female parent, and 165 F1 full-sib progenies through whole-genome resequencing strategy, and subsequently perform comprehensive QTL mapping of six economically important growth-related traits, in order to identify candidate genes underlying growth regulation in L. brachycephalus.

Results: Pearson correlation analysis demonstrated strong associations among all six growth-related traits (r > 0.8, P < 0.001), indicating likely pleiotropic regulation through shared genetic factors. The high-density linkage map for L. brachycephalus incorporated 164,435 high-quality SNPs distributed across 50 linkage groups, achieving complete genome coverage of 6,425.95 cM. The exceptional marker density (average inter-marker distance = 0.10 cM) establishes this as the most precise genetic map reported for this species to date, enabling the accurate candidate gene localization and enhanced marker-assisted selection. Through QTL mapping analysis, several genomic regions significantly associated with growth-related traits were identified based on genome-wide peak logarithm of odds scores. Specifically, one major QTL for body height was located on linkage group (LG27), and two distinct QTL for body weight were positioned on LG20 and LG26. Notably, four longitudinal growth traits (total length, body length, fork length, and preanal body length) were found to co-localize within the same significant QTL interval on LG27. These QTL intervals identified 6.27-39.36% of the phenotypic variance explained for the respective traits. Furthermore, putative candidate genes potentially regulating each target trait were identified through comprehensive analysis of these significant QTL intervals.

Discussion: This integrated approach provides a foundation for marker-assisted selection and enhances the understanding of growth-related genetic mechanisms in this important species.

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来源期刊
Frontiers in Genetics
Frontiers in Genetics Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
5.50
自引率
8.10%
发文量
3491
审稿时长
14 weeks
期刊介绍: Frontiers in Genetics publishes rigorously peer-reviewed research on genes and genomes relating to all the domains of life, from humans to plants to livestock and other model organisms. Led by an outstanding Editorial Board of the world’s leading experts, this multidisciplinary, open-access journal is at the forefront of communicating cutting-edge research to researchers, academics, clinicians, policy makers and the public. The study of inheritance and the impact of the genome on various biological processes is well documented. However, the majority of discoveries are still to come. A new era is seeing major developments in the function and variability of the genome, the use of genetic and genomic tools and the analysis of the genetic basis of various biological phenomena.
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