尽管存在杂交、多样化和生态位转移,但在Galápagos鳞虫适应性辐射中没有转座因子爆发的证据。

IF 4.7 2区 生物学 Q1 GENETICS & HEREDITY
José Cerca, Patricia Jaramillo Díaz, Clément Goubert, Heidi Yang, Vanessa C Bieker, Mario Fernández-Mazuecos, Pablo Vargas, Rowan Schley, Siyu Li, Juan Ernesto Guevara-Andino, Bent Petersen, Gitte Petersen, Neelima R Sinha, Lene R Nielsen, James H Leebens-Mack, Gonzalo Rivas-Torres, Loren H Rieseberg, Michael D Martin
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引用次数: 0

摘要

转座因子(te)被认为通过促进新表型的出现和物种间差异的积累,在推动多样化方面发挥着关键作用。杂交和适应新的生态位已经被提出破坏限制TE增殖的机制,潜在地诱导“TE爆发”,促进TE在基因组上的积累。适应性辐射的快速物种形成和生态多样化特征为研究TE积累与物种形成、多样化、杂交和适应之间的联系提供了独特的机会。本文以Galápagos群岛特有的鳞片属(Asteraceae)的所有15种为研究对象,研究了多样化、杂交或生态位的变化是否与基因组中TE积累的变化有关。我们的分析表明,在鳞鱼物种及其杂交群体中,TE积累几乎没有变化。与气候变化相关的生态位的变化并没有导致TE积累的明显变化,这是一个令人惊讶的发现,因为干旱带来了预期的选择压力,而干旱通常与基因组大小减少有关。我们发现TEs的时间积累没有明显的模式,在类或超家族水平上没有影响。我们的研究结果表明,虽然te在基因座水平上可能在进化中发挥关键作用,但它们与多样化或物种形成的宏观进化关联似乎很弱。与其积极推动进化多样化,TEs可能只是“随波逐流”。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
No evidence of transposable element bursts in the Galápagos Scalesia adaptive radiation despite hybridization, diversification and ecological niche shifts.

Transposable elements (TEs) have been hypothesized to play a pivotal role in driving diversification by facilitating the emergence of novel phenotypes and the accumulation of divergence between species. Hybridization and adaptation to novel niches have been proposed to destabilize mechanisms constraining TE proliferation, potentially inducing a 'TE burst' that promotes TE accumulation on the genome. The rapid speciation and ecological diversification characteristic of adaptive radiations offer a unique opportunity to examine the link between TE accumulation and speciation, diversification, hybridization and adaptation. Here, focusing on all 15 species of the genus Scalesia (Asteraceae), a radiation endemic to the Galápagos Islands, we test whether diversification, hybridization, or shifts in ecological niche are associated with changes in TE accumulation in genomes. Our analyses reveal little to no variation in TE accumulation among Scalesia species nor its hybrid populations. Shifts in ecological niches, linked to climatic variation, did not result in discernible changes in TE accumulation, a surprising finding given the anticipated selective pressure imposed by aridity, a factor often linked to genome size reduction. We found no distinct patterns in the temporal accumulation of TEs, and no effects at the class or superfamily level. Our findings suggest that while TEs may play a key role in evolution at the locus level, their macroevolutionary association with diversification or speciation appears weak. Rather than actively driving evolutionary diversification, TEs may simply be'along for the ride.

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来源期刊
Mobile DNA
Mobile DNA GENETICS & HEREDITY-
CiteScore
8.20
自引率
6.10%
发文量
26
审稿时长
11 weeks
期刊介绍: Mobile DNA is an online, peer-reviewed, open access journal that publishes articles providing novel insights into DNA rearrangements in all organisms, ranging from transposition and other types of recombination mechanisms to patterns and processes of mobile element and host genome evolution. In addition, the journal will consider articles on the utility of mobile genetic elements in biotechnological methods and protocols.
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