基因组证据揭示了 Heliconius 蝴蝶的三种 W 自体融合。

IF 4 2区 生物学 Q1 GENETICS & HEREDITY
PLoS Genetics Pub Date : 2024-07-18 eCollection Date: 2024-07-01 DOI:10.1371/journal.pgen.1011318
Nicol Rueda-M, Carolina Pardo-Diaz, Gabriela Montejo-Kovacevich, W Owen McMillan, Krzysztof M Kozak, Carlos F Arias, Jonathan Ready, Shane McCarthy, Richard Durbin, Chris D Jiggins, Joana I Meier, Camilo Salazar
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引用次数: 0

摘要

在许多动物中,性染色体在进化过程中是易变的,有时会与常染色体融合,形成所谓的新性染色体。性染色体与常染色体的融合被认为可以减少性冲突,促进物种间的适应和生殖隔离。最近,基因组学的进步推动了生命树中此类融合的发现。在这里,我们发现了在经典适应性辐射蝶类(Heliconius butterflies)的蝶亚支系(sapho subclade)中导致新性染色体的多种融合。Heliconius 蝴蝶一般有 21 条染色体,具有很高的同源染色体突变性。然而,鞘蝶亚支系中的五个蝶种的染色体数目差异很大,从21条到60条不等。我们发现,所有这些物种的 W 染色体都与 4 号染色体融合。有两对姐妹种的 W 染色体分别与 9 号或 14 号染色体融合。常染色体和性染色体之间的这些融合使赫利孔乌斯蝴蝶成为研究新性染色体在适应性辐射中的作用以及性染色体随时间退化的理想系统。我们的研究结果表明,即使在性染色体没有明确组装的情况下,短读数重测序也能检测到性染色体与常染色体融合事件的基因组特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genomic evidence reveals three W-autosome fusions in Heliconius butterflies.

Sex chromosomes are evolutionarily labile in many animals and sometimes fuse with autosomes, creating so-called neo-sex chromosomes. Fusions between sex chromosomes and autosomes have been proposed to reduce sexual conflict and to promote adaptation and reproductive isolation among species. Recently, advances in genomics have fuelled the discovery of such fusions across the tree of life. Here, we discovered multiple fusions leading to neo-sex chromosomes in the sapho subclade of the classical adaptive radiation of Heliconius butterflies. Heliconius butterflies generally have 21 chromosomes with very high synteny. However, the five Heliconius species in the sapho subclade show large variation in chromosome number ranging from 21 to 60. We find that the W chromosome is fused with chromosome 4 in all of them. Two sister species pairs show subsequent fusions between the W and chromosomes 9 or 14, respectively. These fusions between autosomes and sex chromosomes make Heliconius butterflies an ideal system for studying the role of neo-sex chromosomes in adaptive radiations and the degeneration of sex chromosomes over time. Our findings emphasize the capability of short-read resequencing to detect genomic signatures of fusion events between sex chromosomes and autosomes even when sex chromosomes are not explicitly assembled.

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来源期刊
PLoS Genetics
PLoS Genetics GENETICS & HEREDITY-
自引率
2.20%
发文量
438
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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