MicroRNA 433 regulates nonsense-mediated mRNA decay by targeting SMG5 mRNA

IF 2.946 Q3 Biochemistry, Genetics and Molecular Biology BMC Molecular Biology Pub Date : 2016-07-29 DOI:10.1186/s12867-016-0070-z
Yi Jin, Fang Zhang, Zhenfa Ma, Zhuqing Ren
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引用次数: 9

Abstract

Nonsense-mediated mRNA decay (NMD) is a RNA quality surveillance system for eukaryotes. It prevents cells from generating deleterious truncated proteins by degrading abnormal mRNAs that harbor premature termination codon (PTC). However, little is known about the molecular regulation mechanism underlying the inhibition of NMD by microRNAs.

The present study demonstrated that miR-433 was involved in NMD pathway via negatively regulating SMG5. We provided evidence that (1) overexpression of miR-433 significantly suppressed the expression of SMG5 (P?<?0.05); (2) Both mRNA and protein expression levels of TBL2 and GADD45B, substrates of NMD, were increased when SMG5 was suppressed by siRNA; (3) Expression of SMG5, TBL2 and GADD45B were significantly increased by miR-433 inhibitor (P?<?0.05). These results together illustrated that miR-433 regulated NMD by targeting SMG5 mRNA.

Our study highlights that miR-433 represses nonsense mediated mRNA decay. The miR-433 targets 3’-UTR of SMG5 and represses the expression of SMG5, whereas NMD activity is decreased when SMG5 is decreased. This discovery provides evidence for microRNA/NMD regulatory mechanism.

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MicroRNA 433通过靶向SMG5 mRNA调控无义介导的mRNA衰变
无义介导的mRNA衰变(NMD)是一种真核生物的RNA质量监测系统。它通过降解含有过早终止密码子(PTC)的异常mrna来防止细胞产生有害的截断蛋白。然而,对microrna抑制NMD的分子调控机制知之甚少。本研究表明,miR-433通过负调控SMG5参与NMD通路。我们提供的证据表明:(1)过表达miR-433显著抑制SMG5的表达(P <?0.05);(2)当siRNA抑制SMG5时,NMD底物TBL2和GADD45B的mRNA和蛋白表达水平均升高;(3) miR-433抑制剂显著提高SMG5、TBL2和GADD45B的表达(P <?0.05)。这些结果共同说明miR-433通过靶向SMG5 mRNA调控NMD。我们的研究强调miR-433抑制无义介导的mRNA衰变。miR-433靶向SMG5的3 ' -UTR,抑制SMG5的表达,而NMD活性随着SMG5的降低而降低。这一发现为microRNA/NMD调控机制提供了证据。
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来源期刊
BMC Molecular Biology
BMC Molecular Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: BMC Molecular Biology is an open access journal publishing original peer-reviewed research articles in all aspects of DNA and RNA in a cellular context, encompassing investigations of chromatin, replication, recombination, mutation, repair, transcription, translation and RNA processing and function.
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