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多个预编辑的 mRNA 中的 G-四链体结构表明 RNA 编辑在原生动物中的进化驱动力。

Multiple G-quartet structures in pre-edited mRNAs suggest evolutionary driving force for RNA editing in trypanosomes.

机构信息

Molecular Genetics, Darmstadt University of Technology, Schnittspahnstraße 10, 64287 Darmstadt, Germany.

出版信息

Sci Rep. 2016 Jul 20;6:29810. doi: 10.1038/srep29810.

Abstract

Mitochondrial transcript maturation in African trypanosomes requires a U-nucleotide specific RNA editing reaction. In its most extreme form hundreds of U's are inserted into and deleted from primary transcripts to generate functional mRNAs. Unfortunately, both origin and biological role of the process have remained enigmatic. Here we report a so far unrecognized structural feature of pre-edited mRNAs. We demonstrate that the cryptic pre-mRNAs contain numerous clustered G-nt, which fold into G-quadruplex (GQ) structures. We identified 27 GQ's in the different pre-mRNAs and demonstrate a positive correlation between the steady state abundance of guide (g)RNAs and the sequence position of GQ-elements. We postulate that the driving force for selecting G-rich sequences lies in the formation of DNA/RNA hybrid G-quadruplex (HQ) structures between the pre-edited transcripts and the non-template strands of mitochondrial DNA. HQ's are transcription termination/replication initiation sites and thus guarantee an unperturbed replication of the mt-genome. This is of special importance in the insect-stage of the parasite. In the transcription-on state, the identified GQ's require editing as a GQ-resolving activity indicating a link between replication, transcription and RNA editing. We propose that the different processes have coevolved and suggest the parasite life-cycle and the single mitochondrion as evolutionary driving forces.

摘要

线粒体转录成熟在非洲锥虫需要一个 U-核苷酸特异性 RNA 编辑反应。在其最极端的形式,数百个 U 被插入和删除从初级转录物生成功能的 mRNAs。不幸的是,过程的起源和生物学作用仍然是神秘的。在这里,我们报告了一个迄今为止未被识别的前编辑 mRNAs 的结构特征。我们证明了隐藏的前 mRNA 包含大量簇状的 G-nt,这些 G-nt 折叠成 G-四链体 (GQ) 结构。我们在不同的前 mRNA 中鉴定了 27 个 GQ,并证明了指导 (g)RNAs 的稳态丰度与 GQ 元件的序列位置之间存在正相关。我们假设选择富含 G 的序列的驱动力在于在编辑前转录物和线粒体 DNA 的非模板链之间形成 DNA/RNA 杂交 G-四链体 (HQ) 结构。HQ 是转录终止/复制起始位点,因此保证了 mt 基因组的无干扰复制。这在寄生虫的昆虫阶段尤为重要。在转录开启状态下,鉴定出的 GQ 需要编辑作为 GQ 解析活性,表明复制、转录和 RNA 编辑之间存在联系。我们提出,不同的过程是共同进化的,并建议寄生虫的生命周期和单个线粒体是进化的驱动力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d523/4951716/de1d94d7456b/srep29810-f1.jpg

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