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基于RNA的转座子表达调控。

RNA-based regulation of transposon expression.

作者信息

Gebert Daniel, Rosenkranz David

机构信息

Institute of Anthropology, Johannes Gutenberg University, Mainz, Germany.

出版信息

Wiley Interdiscip Rev RNA. 2015 Nov-Dec;6(6):687-708. doi: 10.1002/wrna.1310. Epub 2015 Oct 6.

Abstract

Throughout the domains of life, transposon activity represents a serious threat to genome integrity and evolution has realized different molecular mechanisms that aim to inhibit the transposition of mobile DNA. Small noncoding RNAs that function as guides for Argonaute effector proteins represent a key feature of so-called RNA interference (RNAi) pathways and specialized RNAi pathways exist to repress transposon activity on the transcriptional and posttranscriptional level. Transposon transcription can be diminished by targeted DNA methylation or chromatin remodeling via repressive Histone modifications. Posttranscriptional transposon silencing bases on degradation of transposon transcripts to prevent either reverse transcription followed by genomic reintegration or translation into proteins that mediate the transposition process. In plants, Argonaute-like proteins guided by short interfering RNAs (siRNAs) are essential for transposon repression on the epigenetic and posttranscriptional level. In the germline of animals, these tasks are often assumed by a second subclass of Argonaute proteins referred to as Piwi-like proteins, which bind a distinct class of small noncoding RNAs named piwi-interacting RNAs (piRNAs). Though the principals of RNAi pathways are essentially the same in all eukaryotic organisms, remarkable differences can be observed even in closely related species reflecting the astonishing plasticity and diversity of these pathways.

摘要

在整个生命领域中,转座子活性对基因组完整性构成严重威胁,进化过程中产生了不同的分子机制来抑制移动DNA的转座。作为AGO效应蛋白向导的小非编码RNA是所谓RNA干扰(RNAi)途径的关键特征,并且存在专门的RNAi途径在转录和转录后水平抑制转座子活性。转座子转录可通过靶向DNA甲基化或经由抑制性组蛋白修饰的染色质重塑而减弱。转录后转座子沉默基于转座子转录本的降解,以防止逆转录随后的基因组重新整合或翻译为介导转座过程的蛋白质。在植物中,由短干扰RNA(siRNA)引导的AGO样蛋白对于表观遗传和转录后水平的转座子抑制至关重要。在动物的生殖系中,这些任务通常由AGO蛋白的第二个亚类承担,即PIWI样蛋白,其结合一类独特的小非编码RNA,称为PIWI相互作用RNA(piRNA)。尽管RNAi途径的原理在所有真核生物中基本相同,但即使在密切相关的物种中也能观察到显著差异,这反映了这些途径惊人的可塑性和多样性。

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