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miRNA 靶位在编码序列和 3'UTR 中的影响。

The impact of miRNA target sites in coding sequences and in 3'UTRs.

机构信息

Max Delbrück Centrum für Molekulare Medizin, Berlin, Germany.

出版信息

PLoS One. 2011 Mar 22;6(3):e18067. doi: 10.1371/journal.pone.0018067.

Abstract

Animal miRNAs are a large class of small regulatory RNAs that are known to directly and negatively regulate the expression of a large fraction of all protein encoding genes. The identification and characterization of miRNA targets is thus a fundamental problem in biology. miRNAs regulate target genes by binding to 3' untranslated regions (3'UTRs) of target mRNAs, and multiple binding sites for the same miRNA in 3'UTRs can strongly enhance the degree of regulation. Recent experiments have demonstrated that a large fraction of miRNA binding sites reside in coding sequences. Overall, miRNA binding sites in coding regions were shown to mediate smaller regulation than 3'UTR binding. However, possible interactions between target sites in coding sequences and 3'UTRs have not been studied. Using transcriptomics and proteomics data of ten miRNA mis-expression experiments as well as transcriptome-wide experimentally identified miRNA target sites, we found that mRNA and protein expression of genes containing target sites both in coding regions and 3'UTRs were in general mildly but significantly more regulated than those containing target sites in 3'UTRs only. These effects were stronger for conserved target sites of length 7-8 nt in coding regions compared to non-conserved sites. Combined with our other finding that miRNA target sites in coding regions are under negative selection, our results shed light on the functional importance of miRNA targeting in coding regions.

摘要

动物 miRNA 是一大类小的调控 RNA,已知其可以直接和负调控很大一部分编码蛋白的基因的表达。因此,miRNA 靶标的鉴定和描述是生物学中的一个基本问题。miRNA 通过与靶 mRNA 的 3'非翻译区(3'UTRs)结合来调控靶基因,并且在 3'UTRs 中相同 miRNA 的多个结合位点可以强烈增强调控程度。最近的实验表明,很大一部分 miRNA 结合位点位于编码序列中。总的来说,编码区的 miRNA 结合位点介导的调控程度小于 3'UTR 结合。然而,编码序列中靶位点与 3'UTR 之间的可能相互作用尚未被研究。我们使用十个 miRNA 表达异常实验的转录组学和蛋白质组学数据以及全转录组范围内实验鉴定的 miRNA 靶位点,发现包含编码区和 3'UTR 中靶位点的基因的 mRNA 和蛋白质表达通常比仅包含 3'UTR 中靶位点的基因的表达更受调节,尽管这种调节是轻微的,但具有统计学意义。对于长度为 7-8nt 的保守靶位点,这种效应在编码区比非保守靶位点更强。结合我们的另一个发现,即编码区的 miRNA 靶位点受到负选择,我们的结果揭示了 miRNA 在编码区靶向的功能重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84a9/3062573/05495f8b8bc7/pone.0018067.g001.jpg

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