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真核生物中的巨型转座子:更大是否更好?

Giant Transposons in Eukaryotes: Is Bigger Better?

机构信息

Josephine Bay Paul Center for Comparative Molecular Biology and Evolution, Marine Biological Laboratory, Woods Hole, Massachusetts.

出版信息

Genome Biol Evol. 2019 Mar 1;11(3):906-918. doi: 10.1093/gbe/evz041.

Abstract

Transposable elements (TEs) are ubiquitous in both prokaryotes and eukaryotes, and the dynamic character of their interaction with host genomes brings about numerous evolutionary innovations and shapes genome structure and function in a multitude of ways. In traditional classification systems, TEs are often being depicted in simplistic ways, based primarily on the key enzymes required for transposition, such as transposases/recombinases and reverse transcriptases. Recent progress in whole-genome sequencing and long-read assembly, combined with expansion of the familiar range of model organisms, resulted in identification of unprecedentedly long transposable units spanning dozens or even hundreds of kilobases, initially in prokaryotic and more recently in eukaryotic systems. Here, we focus on such oversized eukaryotic TEs, including retrotransposons and DNA transposons, outline their complex and often combinatorial nature and closely intertwined relationship with viruses, and discuss their potential for participating in transfer of long stretches of DNA in eukaryotes.

摘要

转座元件 (TEs) 在原核生物和真核生物中普遍存在,其与宿主基因组相互作用的动态特征带来了许多进化创新,并以多种方式塑造了基因组的结构和功能。在传统的分类系统中,TEs 通常是以简单的方式来描述的,主要基于转座所需的关键酶,如转座酶/重组酶和逆转录酶。全基因组测序和长读长组装的最新进展,加上常见模式生物范围的扩大,导致了以前所未有的数十甚至数百个千碱基长的转座单元的识别,最初在原核生物中,最近在真核生物系统中也是如此。在这里,我们专注于这种超大的真核 TEs,包括逆转录转座子和 DNA 转座子,概述它们的复杂且通常是组合性质,以及与病毒的紧密交织关系,并讨论它们在真核生物中参与长片段 DNA 转移的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4520/6431247/85e0015936e8/evz041f1.jpg

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