{"title":"MicroRNA 433 regulates nonsense-mediated mRNA decay by targeting SMG5 mRNA","authors":"Yi Jin, Fang Zhang, Zhenfa Ma, Zhuqing Ren","doi":"10.1186/s12867-016-0070-z","DOIUrl":null,"url":null,"abstract":"<p>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.</p><p>The present study demonstrated that miR-433 was involved in NMD pathway via negatively regulating <i>SMG5</i>. We provided evidence that (1) overexpression of miR-433 significantly suppressed the expression of <i>SMG5</i> (P?<?0.05); (2) Both mRNA and protein expression levels of <i>TBL2</i> and <i>GADD45B</i>, substrates of NMD, were increased when <i>SMG5</i> was suppressed by siRNA; (3) Expression of <i>SMG5</i>, <i>TBL2</i> and <i>GADD45B</i> were significantly increased by miR-433 inhibitor (P?<?0.05). These results together illustrated that miR-433 regulated NMD by targeting <i>SMG5</i> mRNA.</p><p>Our study highlights that miR-433 represses nonsense mediated mRNA decay. The miR-433 targets 3’-UTR of <i>SMG5</i> and represses the expression of <i>SMG5</i>, whereas NMD activity is decreased when SMG5 is decreased. This discovery provides evidence for microRNA/NMD regulatory mechanism.</p>","PeriodicalId":497,"journal":{"name":"BMC Molecular Biology","volume":"17 1","pages":""},"PeriodicalIF":2.9460,"publicationDate":"2016-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12867-016-0070-z","citationCount":"9","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Molecular Biology","FirstCategoryId":"1085","ListUrlMain":"https://link.springer.com/article/10.1186/s12867-016-0070-z","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
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.
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.