小有效规模种群中数量性状核苷酸的 SNP 图谱及其对制图和基因组预测的影响。

IF 3.3 3区 生物学 Q2 GENETICS & HEREDITY
Genetics Pub Date : 2024-08-07 DOI:10.1093/genetics/iyae103
Ivan Pocrnic, Daniela Lourenco, Ignacy Misztal
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引用次数: 0

摘要

通过纳入序列信息来增加 SNP 密度只能在一定程度上提高家畜育种值的预测准确性。为了找出原因,我们利用统计模型和模拟研究了有效种群规模(Ne)较小的种群中数量性状核苷酸(QTN)周围估计 SNP 效应的分布形状(轮廓)。通过平均每个 QTN 周围的 SNP 效应创建的 QTN 剖面与基于 Ne 和 SNP 之间遗传距离的预期配对连锁不平衡(PLD)的形状相似,QTN 有一个明显的峰值。Ne 较小的人群显示出较低但较宽的 QTN 曲线。然而,增加更多具有表型的基因分型个体会使剖面更接近 QTN。与 Ne 较小的人群相比,Ne 较大的人群的 QTN 曲线更高、更窄。假设 QTN 曲线为 PLD 曲线,则每个 QTN 所解释的加性遗传变异的 80% 都包含在 QTN 周围的 ± 1/Ne Morgan 区间内,在牛中相当于 2 Mb,在猪和鸡中相当于 5 Mb。由于区间如此之大,即使所有 QTN 都在数据中,而且假定的遗传结构非常简单,也很难识别 QTN。QTN 检测的其他复杂性来自 QTN 图谱与关系信号的混杂、与间隔较近的 QTN 重叠的图谱以及虚假信号。不过,即使没有 QTN 识别,小 Ne 也能通过大数据进行准确预测,因为如果 SNP 密度足以使片段饱和,QTN 剖面就能解释 QTN。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Single nucleotide polymorphism profile for quantitative trait nucleotide in populations with small effective size and its impact on mapping and genomic predictions.

Increasing SNP density by incorporating sequence information only marginally increases prediction accuracies of breeding values in livestock. To find out why, we used statistical models and simulations to investigate the shape of distribution of estimated SNP effects (a profile) around quantitative trait nucleotides (QTNs) in populations with a small effective population size (Ne). A QTN profile created by averaging SNP effects around each QTN was similar to the shape of expected pairwise linkage disequilibrium (PLD) based on Ne and genetic distance between SNP, with a distinct peak for the QTN. Populations with smaller Ne showed lower but wider QTN profiles. However, adding more genotyped individuals with phenotypes dragged the profile closer to the QTN. The QTN profile was higher and narrower for populations with larger compared to smaller Ne. Assuming the PLD curve for the QTN profile, 80% of the additive genetic variance explained by each QTN was contained in ± 1/Ne Morgan interval around the QTN, corresponding to 2 Mb in cattle and 5 Mb in pigs and chickens. With such large intervals, identifying QTN is difficult even if all of them are in the data and the assumed genetic architecture is simplistic. Additional complexity in QTN detection arises from confounding of QTN profiles with signals due to relationships, overlapping profiles with closely spaced QTN, and spurious signals. However, small Ne allows for accurate predictions with large data even without QTN identification because QTNs are accounted for by QTN profiles if SNP density is sufficient to saturate the segments.

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来源期刊
Genetics
Genetics GENETICS & HEREDITY-
CiteScore
6.90
自引率
6.10%
发文量
177
审稿时长
1.5 months
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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