真核生物基因组中转座因子的进化动力学。

Genome dynamics Pub Date : 2012-01-01 Epub Date: 2012-06-25 DOI:10.1159/000337126
M Tollis, S Boissinot
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引用次数: 41

摘要

转座因子(te)是真核生物基因组中普遍存在的成分。它们在很大程度上影响了它们的大小、结构和功能。大量真核生物基因组的测序揭示了真核生物之间te的丰度和多样性的一些显著差异。原生生物、植物、昆虫和脊椎动物中既有te数量多的物种,也有te数量少的物种,也有te数量多样的物种和te多样性有限的物种。生物体的复杂性与其TE特征之间没有明显的关系。TE的多样性和丰度是转位率、对新插入物的选择强度、种群的人口统计学历史和DNA损失率之间相互作用的结果。最近的群体遗传学研究表明,对新插入物的选择(主要是由te介导异位重组事件的能力引起的)限制了te的固定,但群体瓶颈或近亲繁殖导致的有效群体规模的减少显著降低了选择的效力。这些结果强调了漂移在形成基因组结构中的重要性。
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The evolutionary dynamics of transposable elements in eukaryote genomes.

Transposable elements (TEs) are ubiquitous components of eukaryotic genomes. They have considerably affected their size, structure and function. The sequencing of a multitude of eukaryote genomes has revealed some striking differences in the abundance and diversity of TEs among eukaryotes. Protists, plants, insects and vertebrates contain species with large numbers of TEs and species with small numbers, as well as species with diverse repertoires of TEs and species with a limited diversity of TEs. There is no apparent relationship between the complexity of organisms and their TE profile. The profile of TE diversity and abundance results from the interaction between the rate of transposition, the intensity of selection against new inserts, the demographic history of populations and the rate of DNA loss. Recent population genetics studies suggest that selection against new insertions, mostly caused by the ability of TEs to mediate ectopic recombination events, is limiting the fixation of TEs, but that reduction in effective population size, caused by population bottlenecks or inbreeding, significantly reduces the efficacy of selection. These results emphasize the importance of drift in shaping genomic architecture.

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The evolutionary dynamics of transposable elements in eukaryote genomes. SINEs as driving forces in genome evolution. Unstable microsatellite repeats facilitate rapid evolution of coding and regulatory sequences. Satellite DNA evolution. Satellite DNA-mediated effects on genome regulation.
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