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假基因通过ceRNA网络调控亲本基因表达。

Pseudogenes regulate parental gene expression via ceRNA network.

作者信息

An Yang, Furber Kendra L, Ji Shaoping

机构信息

Department of Biochemistry and Molecular Biology, Medical School, Henan University, Henan Province, China.

College of Pharmacy and Nutrition, University of Saskatchewan, Saskatchewan, SK, Canada.

出版信息

J Cell Mol Med. 2017 Jan;21(1):185-192. doi: 10.1111/jcmm.12952. Epub 2016 Aug 25.

Abstract

The concept of competitive endogenous RNA (ceRNA) was first proposed by Salmena and colleagues. Evidence suggests that pseudogene RNAs can act as a 'sponge' through competitive binding of common miRNA, releasing or attenuating repression through sequestering miRNAs away from parental mRNA. In theory, ceRNAs refer to all transcripts such as mRNA, tRNA, rRNA, long non-coding RNA, pseudogene RNA and circular RNA, because all of them may become the targets of miRNA depending on spatiotemporal situation. As binding of miRNA to the target RNA is not 100% complementary, it is possible that one miRNA can bind to multiple target RNAs and vice versa. All RNAs crosstalk through competitively binding to miRNAvia miRNA response elements (MREs) contained within the RNA sequences, thus forming a complex regulatory network. The ratio of a subset of miRNAs to the corresponding number of MREs determines repression strength on a given mRNA translation or stability. An increase in pseudogene RNA level can sequester miRNA and release repression on the parental gene, leading to an increase in parental gene expression. A massive number of transcripts constitute a complicated network that regulates each other through this proposed mechanism, though some regulatory significance may be mild or even undetectable. It is possible that the regulation of gene and pseudogene expression occurring in this manor involves all RNAs bearing common MREs. In this review, we will primarily discuss how pseudogene transcripts regulate expression of parental genes via ceRNA network and biological significance of regulation.

摘要

竞争性内源RNA(ceRNA)的概念最早由萨尔梅纳及其同事提出。有证据表明,假基因RNA可通过竞争性结合常见的微小RNA(miRNA)发挥“海绵”作用,通过将miRNA从亲本mRNA上隔离来释放或减弱抑制作用。理论上,ceRNA指所有转录本,如mRNA、tRNA、rRNA、长链非编码RNA、假基因RNA和环状RNA,因为它们都可能根据时空情况成为miRNA的靶标。由于miRNA与靶标RNA的结合并非100%互补,所以一个miRNA有可能结合多个靶标RNA,反之亦然。所有RNA通过RNA序列中包含的miRNA反应元件(MRE)竞争性结合miRNA进行相互作用,从而形成一个复杂的调控网络。miRNA子集与相应MRE数量的比例决定了对给定mRNA翻译或稳定性的抑制强度。假基因RNA水平的增加可隔离miRNA并解除对亲本基因的抑制,导致亲本基因表达增加。大量转录本构成了一个复杂的网络,通过这种机制相互调节,尽管一些调节意义可能很微弱甚至无法检测到。以这种方式发生的基因和假基因表达调控可能涉及所有带有共同MRE的RNA。在本综述中,我们将主要讨论假基因转录本如何通过ceRNA网络调控亲本基因的表达以及调控的生物学意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5585/5192809/a0d663ee8a76/JCMM-21-185-g001.jpg

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