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反义转录本如何进化为编码新蛋白。

How antisense transcripts can evolve to encode novel proteins.

机构信息

Institute for Evolution and Biodiversity, University of Münster, Hüfferstrasse 1, Münster, Germany.

Aix-Marseille Université, INSERM, TAGC, Marseille, France.

出版信息

Nat Commun. 2024 Jul 23;15(1):6187. doi: 10.1038/s41467-024-50550-3.

Abstract

Protein coding features can emerge de novo in non coding transcripts, resulting in emergence of new protein coding genes. Studies across many species show that a large fraction of evolutionarily novel non-coding RNAs have an antisense overlap with protein coding genes. The open reading frames (ORFs) in these antisense RNAs could also overlap with existing ORFs. In this study, we investigate how the evolution an ORF could be constrained by its overlap with an existing ORF in three different reading frames. Using a combination of mathematical modeling and genome/transcriptome data analysis in two different model organisms, we show that antisense overlap can increase the likelihood of ORF emergence and reduce the likelihood of ORF loss, especially in one of the three reading frames. In addition to rationalising the repeatedly reported prevalence of de novo emerged genes in antisense transcripts, our work also provides a generic modeling and an analytical framework that can be used to understand evolution of antisense genes.

摘要

蛋白质编码特征可以从头出现在非编码转录本中,从而产生新的蛋白质编码基因。许多物种的研究表明,很大一部分进化上新颖的非编码 RNA 与蛋白质编码基因具有反义重叠。这些反义 RNA 中的开放阅读框(ORF)也可能与现有的 ORF 重叠。在这项研究中,我们研究了 ORF 的进化如何受到其与现有 ORF 在三个不同阅读框中的重叠的限制。我们使用两种不同模式生物的数学建模和基因组/转录组数据分析的组合,表明反义重叠可以增加 ORF 出现的可能性,并降低 ORF 丢失的可能性,尤其是在三个阅读框中的一个中。除了合理化反义转录本中反复报道的新出现基因的普遍性之外,我们的工作还提供了一个通用的建模和分析框架,可用于理解反义基因的进化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3eb2/11266595/07bec700ac5d/41467_2024_50550_Fig1_HTML.jpg

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