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线粒体 RNA 成熟。

Mitochondrial RNA maturation.

机构信息

Wellcome Centre for Mitochondrial Research, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.

出版信息

RNA Biol. 2024 Jan;21(1):28-39. doi: 10.1080/15476286.2024.2414157. Epub 2024 Oct 10.

Abstract

The vast majority of oxygen-utilizing eukaryotes need to express their own mitochondrial genome, mtDNA, to survive. In comparison to size of their nuclear genome, mtDNA is minimal, even in the most exceptional examples. Having evolved from bacteria in an endosymbiotic event, it might be expected that the process of mtDNA expression would be relatively simple. The aim of this short review is to illustrate just how wrong this assumption is. The production of functional mitochondrial RNA across species evolved in many directions. Organelles use a dizzying array of RNA processing, modifying, editing, splicing and maturation events that largely require the import of nuclear-encoded proteins from the cytosol. These processes are sometimes driven by the unusual behaviour of the mitochondrial genome from which the RNA is originally transcribed, but in many examples the complex processes that are essential for the production of functional RNA in the organelle, are fascinating and bewildering.

摘要

绝大多数需氧真核生物需要表达自己的线粒体基因组 mtDNA 才能存活。与核基因组的大小相比,mtDNA 非常小,即使是在最特殊的例子中也是如此。它是从内共生事件中的细菌进化而来的,因此可以预期 mtDNA 表达的过程相对简单。本文的目的是说明这种假设是多么错误。跨物种的功能性线粒体 RNA 的产生在许多方向上进化。细胞器使用令人眼花缭乱的 RNA 加工、修饰、编辑、剪接和成熟事件,这些事件在很大程度上需要从细胞质中导入核编码蛋白。这些过程有时是由最初转录 RNA 的线粒体基因组的异常行为驱动的,但在许多例子中,对于细胞器中功能性 RNA 的产生至关重要的复杂过程既迷人又令人困惑。

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