估计等位基因频率的特定规模和局部空间模式。

IF 3.3 3区 生物学 Q2 GENETICS & HEREDITY
Genetics Pub Date : 2024-07-08 DOI:10.1093/genetics/iyae082
Jesse R Lasky, Margarita Takou, Diana Gamba, Timothy H Keitt
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引用次数: 0

摘要

描述等位基因频率的空间模式是进化生物学的基础,因为这些模式包含了潜在过程的证据。然而,基因流动、选择变化和漂移作用的空间尺度往往是未知的。这些过程中的许多过程在整个空间的运作可能不一致,从而导致非稳态模式。我们提出了一种小波方法来描述等位基因频率的空间模式,有助于解决这些问题。我们展示了我们的方法如何在多个空间尺度上描述亲缘关系的空间模式,即多焦点小波遗传相似性。我们还开发了等位基因频率和数量性状位点(QTL)空间分异的小波检验。通过模拟,我们说明了这些方法在不同情况下的应用。我们还将我们的方法应用于拟南芥的自然种群,以描述种群结构并识别跨尺度的局部适应基因座。例如,我们发现拟南芥开花时间 QTL 在 300 至 1300 千米尺度上显示出显著的遗传分化。等位基因频率的小波变换为揭示地理模式和潜在的进化过程提供了一种灵活的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Estimating scale-specific and localized spatial patterns in allele frequency.

Characterizing spatial patterns in allele frequencies is fundamental to evolutionary biology because these patterns contain evidence of underlying processes. However, the spatial scales at which gene flow, changing selection, and drift act are often unknown. Many of these processes can operate inconsistently across space, causing nonstationary patterns. We present a wavelet approach to characterize spatial pattern in allele frequency that helps solve these problems. We show how our approach can characterize spatial patterns in relatedness at multiple spatial scales, i.e. a multilocus wavelet genetic dissimilarity. We also develop wavelet tests of spatial differentiation in allele frequency and quantitative trait loci (QTL). With simulation, we illustrate these methods under different scenarios. We also apply our approach to natural populations of Arabidopsis thaliana to characterize population structure and identify locally adapted loci across scales. We find, for example, that Arabidopsis flowering time QTL show significantly elevated genetic differentiation at 300-1,300 km scales. Wavelet transforms of allele frequencies offer a flexible way to reveal geographic patterns and underlying evolutionary processes.

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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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