深海喷口嗜热蠕虫属物种形成早期和晚期分化的基因组模式。

Camille Thomas-Bulle, Denis Bertrand, Niranjan Nagarajan, Richard R Copley, Erwan Corre, Stéphane Hourdez, Éric Bonnivard, Adam Claridge-Chang, Didier Jollivet
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引用次数: 3

摘要

背景:海脊俯冲、板块碰撞和新裂谷形成的深海热液环境的短暂性和破碎性,目前正在分离喷口种群,促进局部适应,并促进物种形成和物种特化的爆发。管栖蠕虫Alvinella pompejana称为庞贝蠕虫和它的姊妹物种A. caudata在东太平洋隆起的深海热液烟囱的最热部分整体生活。它们暴露在极端的温度和化学梯度下,这些梯度在空间和时间上变化很大,因此是了解喷口动物进化机制的理想候选者。结果:我们利用转录组组装和基因组初稿探索了这些代表性蠕虫物种形成早期和晚期的基因组分化模式,以更好地了解地理隔离和栖息地偏好在其基因组进化中的相对作用。对庞培阿尔维尼亚(Alvinella pompejana)(分离早期)和庞培阿尔维尼亚(Alvinella caudata)(种形成后期)之间的异域居群进行了分析。我们首先确定了不同的基因组区域和选择目标,以及它们在基因组中同源基因集合中的位置,然后通过记录分离过程中最不同和/或积极选择的基因的注释来描述物种形成动力学。基因作图清楚地表明,与物种形成早期相关的分化基因虽然占基因总数的近30%,但在基因组中高度分散,不存在分化岛,不参与配子识别和核分裂不相容。相比之下,庞培蒿和尾蒿的基因组明显分离,几乎所有基因(96%)都表现出高度分化。然而,这种凝结效应似乎与栖息地专业化有关,并且仍然允许对参与配子识别的基因进行积极选择,作为物种强化的可能的长期过程。结论:我们的分析强调了自然选择在深海热液烟囱壁上生活的标志性嗜热蠕虫物种形成的早期和晚期阶段的不可忽视的作用。它们揭示了在很长一段时间内物种形成和物种特化过程中基因分化的进化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Genomic patterns of divergence in the early and late steps of speciation of the deep-sea vent thermophilic worms of the genus Alvinella.

Genomic patterns of divergence in the early and late steps of speciation of the deep-sea vent thermophilic worms of the genus Alvinella.

Genomic patterns of divergence in the early and late steps of speciation of the deep-sea vent thermophilic worms of the genus Alvinella.

Genomic patterns of divergence in the early and late steps of speciation of the deep-sea vent thermophilic worms of the genus Alvinella.

Background: The transient and fragmented nature of the deep-sea hydrothermal environment made of ridge subduction, plate collision and the emergence of new rifts is currently acting to separate of vent populations, promoting local adaptation and contributing to bursts of speciation and species specialization. The tube-dwelling worms Alvinella pompejana called the Pompeii worm and its sister species A. caudata live syntopically on the hottest part of deep-sea hydrothermal chimneys along the East Pacific Rise. They are exposed to extreme thermal and chemical gradients, which vary greatly in space and time, and thus represent ideal candidates for understanding the evolutionary mechanisms at play in the vent fauna evolution.

Results: We explored genomic patterns of divergence in the early and late stages of speciation of these emblematic worms using transcriptome assemblies and the first draft genome to better understand the relative role of geographic isolation and habitat preference in their genome evolution. Analyses were conducted on allopatric populations of Alvinella pompejana (early stage of separation) and between A. pompejana and its syntopic species Alvinella caudata (late stage of speciation). We first identified divergent genomic regions and targets of selection as well as their position in the genome over collections of orthologous genes and, then, described the speciation dynamics by documenting the annotation of the most divergent and/or positively selected genes involved in the isolation process. Gene mapping clearly indicated that divergent genes associated with the early stage of speciation, although accounting for nearly 30% of genes, are highly scattered in the genome without any island of divergence and not involved in gamete recognition or mito-nuclear incompatibilities. By contrast, genomes of A. pompejana and A. caudata are clearly separated with nearly all genes (96%) exhibiting high divergence. This congealing effect however seems to be linked to habitat specialization and still allows positive selection on genes involved in gamete recognition, as a possible long-duration process of species reinforcement.

Conclusion: Our analyses highlight the non-negligible role of natural selection on both the early and late stages of speciation in the iconic thermophilic worms living on the walls of deep-sea hydrothermal chimneys. They shed light on the evolution of gene divergence during the process of speciation and species specialization over a very long period of time.

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