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ALU 介导的 A-to-I RNA 编辑:数以百万计的位点和众多悬而未决的问题。

ALU A-to-I RNA Editing: Millions of Sites and Many Open Questions.

机构信息

Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat Gan, Israel.

出版信息

Methods Mol Biol. 2021;2181:149-162. doi: 10.1007/978-1-0716-0787-9_9.

Abstract

Alu elements are repetitive short interspersed elements prevalent in the primate genome. These repeats account for over 10% of the genome with more than a million highly similar copies. A direct outcome of this is an enrichment in long structures of stable dsRNA, which are the target of adenosine deaminases acting on RNAs (ADARs), the enzymes catalyzing A-to-I RNA editing. Indeed, A-to-I editing by ADARs is extremely abundant in primates: over a hundred million editing sites exist in their genomes. However, despite the radical increase in ADAR targets brought on by the introduction of Alu elements, the few evolutionary conserved editing sites manage to retain their editing levels. Here, we review and discuss the cost of having an unusual amount of dsRNA and editing in the transcriptome, as well as the opportunities it presents, which possibly contributed to accelerating primate evolution.

摘要

Alu 元件是普遍存在于灵长类基因组中的重复短散在元件。这些重复序列占基因组的 10%以上,有超过 100 万个高度相似的拷贝。其直接结果是富含稳定的双链 RNA(long structures of stable dsRNA),双链 RNA 是腺苷脱氨酶作用于 RNA 的靶点(adenosine deaminases acting on RNAs, ADARs),ADARs 是催化 A 到 I RNA 编辑的酶。事实上,ADARs 的 A 到 I 编辑在灵长类动物中非常丰富:它们的基因组中存在超过一亿个编辑位点。然而,尽管 Alu 元件的引入使 ADAR 的靶标数量急剧增加,但少数进化保守的编辑位点设法保持其编辑水平。在这里,我们回顾和讨论了在转录组中存在大量双链 RNA 和编辑的代价,以及它所带来的机会,这可能有助于加速灵长类动物的进化。

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