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Pif1 解旋酶和转座子 Helitrons 的原核起源证据。

Pif1 Helicases and the Evidence for a Prokaryotic Origin of Helitrons.

机构信息

Departamento de Genética, Ecologia e Evolução, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

出版信息

Mol Biol Evol. 2022 Jan 7;39(1). doi: 10.1093/molbev/msab334.

DOI:10.1093/molbev/msab334
PMID:34850089
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8788227/
Abstract

Helitrons are the only group of rolling-circle transposons that encode a transposase with a helicase domain (Hel), which belongs to the Pif1 family. Because Pif1 helicases are important components of eukaryotic genomes, it has been suggested that Hel domains probably originated after a host eukaryotic Pif1 gene was captured by a Helitron ancestor. However, the few analyses exploring the evolution of Helitron transposases (RepHel) have focused on its Rep domain, which is also present in other mobile genetic elements. Here, we used phylogenetic and nonmetric multidimensional scaling analyses to investigate the relationship between Hel domains and Pif1-like helicases from a variety of organisms. Our results reveal that Hel domains are only distantly related to genomic helicases from eukaryotes and prokaryotes, and thus are unlikely to have originated from a captured Pif1 gene. Based on this evidence, and on recent studies indicating that Rep domains are more closely related to rolling-circle plasmids and phages, we suggest that Helitrons are descendants of a RepHel-encoding prokaryotic plasmid element that invaded eukaryotic genomes before the radiation of its major groups. We discuss how a Pif1-like helicase domain might have favored the transposition of Helitrons in eukaryotes beyond simply unwinding DNA intermediates. Finally, we demonstrate that some examples in the literature describing genomic helicases from eukaryotes actually consist of Hel domains from Helitrons, a finding that underscores how transposons can hamper the analysis of eukaryotic genes. This investigation also revealed that two groups of land plants appear to have lost genomic Pif1 helicases independently.

摘要

转座子是唯一编码具有解旋酶结构域(Hel)的转座酶的滚环转座子,属于 Pif1 家族。由于 Pif1 解旋酶是真核基因组的重要组成部分,因此有人认为 Hel 结构域可能起源于宿主真核 Pif1 基因被 Helitron 祖先捕获之后。然而,少数探索 Helitron 转座酶(RepHel)进化的分析主要集中在其 Rep 结构域上,该结构域也存在于其他移动遗传元件中。在这里,我们使用系统发育和非度量多维标度分析来研究各种生物体的 Hel 结构域和 Pif1 样解旋酶之间的关系。我们的结果表明,Hel 结构域与真核生物和原核生物的基因组解旋酶仅有远亲关系,因此不太可能起源于捕获的 Pif1 基因。基于这一证据,以及最近的研究表明 Rep 结构域与滚环质粒和噬菌体更为密切相关,我们认为 Helitrons 是编码 RepHel 的原核质粒元件的后代,该元件在其主要类群辐射之前入侵了真核生物基因组。我们讨论了 Pif1 样解旋酶结构域如何在真核生物中转录 Helitrons,而不仅仅是解开 DNA 中间体。最后,我们证明文献中描述的一些真核生物基因组解旋酶实际上是由 Helitrons 的 Hel 结构域组成的,这一发现强调了转座子如何阻碍真核基因的分析。这项研究还表明,两组陆地植物似乎独立地失去了基因组 Pif1 解旋酶。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3385/8788227/7b8a5743a176/msab334f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3385/8788227/e53846b158ed/msab334f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3385/8788227/cbd1c9aabc67/msab334f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3385/8788227/c0bc7f95951d/msab334f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3385/8788227/4e503e6d27f4/msab334f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3385/8788227/992c3ced6e8d/msab334f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3385/8788227/7b8a5743a176/msab334f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3385/8788227/e53846b158ed/msab334f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3385/8788227/cbd1c9aabc67/msab334f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3385/8788227/c0bc7f95951d/msab334f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3385/8788227/4e503e6d27f4/msab334f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3385/8788227/992c3ced6e8d/msab334f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3385/8788227/7b8a5743a176/msab334f6.jpg

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本文引用的文献

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