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端粒 TART 元件在果蝇中靶向 piRNA 机制。

Telomeric TART elements target the piRNA machinery in Drosophila.

机构信息

Department of Genetics, Human Genetics Institute of New Jersey, Rutgers, The State University of New Jersey, Piscataway, New Jersey, United States of America.

出版信息

PLoS Biol. 2020 Dec 21;18(12):e3000689. doi: 10.1371/journal.pbio.3000689. eCollection 2020 Dec.

Abstract

Coevolution between transposable elements (TEs) and their hosts can be antagonistic, where TEs evolve to avoid silencing and the host responds by reestablishing TE suppression, or mutualistic, where TEs are co-opted to benefit their host. The TART-A TE functions as an important component of Drosophila telomeres but has also reportedly inserted into the Drosophila melanogaster nuclear export factor gene nxf2. We find that, rather than inserting into nxf2, TART-A has actually captured a portion of nxf2 sequence. We show that TART-A produces abundant Piwi-interacting small RNAs (piRNAs), some of which are antisense to the nxf2 transcript, and that the TART-like region of nxf2 is evolving rapidly. Furthermore, in D. melanogaster, TART-A is present at higher copy numbers, and nxf2 shows reduced expression, compared to the closely related species Drosophila simulans. We propose that capturing nxf2 sequence allowed TART-A to target the nxf2 gene for piRNA-mediated repression and that these 2 elements are engaged in antagonistic coevolution despite the fact that TART-A is serving a critical role for its host genome.

摘要

转座元件 (TEs) 与其宿主之间的共同进化可能是对抗性的,TEs 进化以避免沉默,而宿主则通过重新建立 TE 抑制来做出反应,或者是互利的,TEs 被共同利用以造福其宿主。TART-A TE 作为果蝇端粒的重要组成部分,但也有报道称其插入到果蝇核输出因子基因 nxf2 中。我们发现,TART-A 并没有插入 nxf2 基因,而是实际上捕获了 nxf2 序列的一部分。我们表明,TART-A 产生大量 Piwi 相互作用的小 RNA (piRNAs),其中一些与 nxf2 转录本反义,并且 nxf2 的 TART 样区域正在快速进化。此外,与亲缘关系密切的物种果蝇 simulans 相比,在 D. melanogaster 中,TART-A 的拷贝数更高,nxf2 的表达水平降低。我们提出,捕获 nxf2 序列使 TART-A 能够针对 nxf2 基因进行 piRNA 介导的抑制,尽管 TART-A 对其宿主基因组起着至关重要的作用,但这 2 个元件仍处于对抗性的共同进化中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4682/7785250/837d8dd0c6a1/pbio.3000689.g001.jpg

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