小rna的一个亚类由蛋白质编码基因的外显子编码。

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Tyron Chang, Dustin C Hancks
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引用次数: 0

摘要

背景:小rna在整个生命之树的物种中调节基因表达。mirna影响多种细胞和生理过程,从发育和应激适应到宿主防御,是最具特征的小RNA类别之一。许多mirna是由宿主基因通过一系列RNA切割反应产生的较长非编码转录本产生的。小RNA在宿主基因中的位置可以决定成熟小RNA的加工过程。例如,一种来自宿主基因内含子序列的mirna,被称为miRtrons,是不依赖于drosha的,并且依赖于剪接来进行生物发生。与此相关,从蛋白质编码mRNA的外显子加工小RNA,原则上可能使其不稳定并损害宿主基因的翻译。在广泛的转录组分析之前,信息学分析确定了6个嵌入蛋白质编码基因外显子的人类mirna,实验研究还发现了其他轶事例子。尽管如此,考虑到现在公认的转录组的复杂性,编码小rna的蛋白质编码mrna是否代表了宿主基因的一个可观类别尚不清楚。结果:我们的分析发现201个小rna(118个人和83个小鼠)由蛋白编码基因(5'-UTR, CDS, 3'-UTR)的外显子编码。其中46例(29例人类和17例小鼠)也存在于MirGeneDB中,其中包括最新的miRNA分类。这些小rna中有96%的蛋白质编码宿主基因关系是以前不知道的。此外,在规范orf编码外显子内嵌入近50个人类和小鼠小rna的鉴定表明,重叠杂交基因可能比以前在高等生物中认识到的更为普遍。对这些小rna子集的表达分析表明,许多小rna在人体组织中表现出差异表达,其模式与候选蛋白编码宿主基因的表达显著相关。意义:总的来说,我们的分析表明,作为宿主基因的蛋白质编码转录物的数量比以前认识到的要多。我们的小RNA宿主基因分类可能为小RNA生物学、特定宿主基因和基因调控提供新的线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A subclass of small RNAs is encoded by exons of protein-coding genes.

Background: Small RNAs regulate gene expression in species across the tree of life. miRNAs, which impact a variety of cellular and physiological processes ranging from development and stress adaptation to host defense, are one of the best characterized classes of small RNA. Many miRNAs are produced from longer non-coding transcripts generated from host genes via a series of RNA cleavage reactions. The location of a small RNA within a host gene can shape the processing of the mature small RNA. For example, a type of miRNAs derived from host gene intronic sequence, referred to as miRtrons, are Drosha-independent and reliant on splicing for biogenesis. Relatedly, processing of a small RNA from an exon of a protein-coding mRNA, in principle, may destabilize it and compromise translation of the host gene. Prior to extensive transcriptome analysis, informatics analyses identified six human miRNAs embedded in exons of protein-coding genes and experimental studies have characterized additional anecdotal examples. Still, whether protein-coding mRNAs encoding small RNAs represent an appreciable class of host genes given the now recognized complexity of the transcriptome is unclear.

Results: Our analysis finds 201 small RNAs (118 human and 83 mouse) encoded by expressed exons of protein-coding genes (5'-UTR, CDS, 3'-UTR). Forty-six of these cases (29 human and 17 mouse) are also present in MirGeneDB which includes the most up-to-date miRNA classifications. Many of these small RNAs are poorly characterized with 96% of the protein-coding host gene relationships identified here not previously known. Furthermore, the identification of nearly fifty human and mouse small RNAs embedded within coding exons of canonical ORFs suggests that overlapping hybrid genes might be more common than previously appreciated in higher organisms. Expression analysis for a subset of these small RNAs indicates that many display differential expression across human tissues with the pattern correlating significantly with the expression of the candidate protein-coding host gene.

Significance: Overall, our analysis suggests that the number of protein-coding transcripts serving as host genes is greater than previously recognized. Our small RNA host gene classifications may serve as a resource to shed new light on small RNA biology, specific host genes, and gene regulation.

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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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