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

被引:7
|
作者
Jin, Yi [1 ,2 ,3 ]
Zhang, Fang [1 ,2 ]
Ma, Zhenfa [1 ,2 ]
Ren, Zhuqing [1 ,2 ,3 ]
机构
[1] Huazhong Agr Univ, Minist Agr, Key Lab Swine Genet & Breeding, Coll Anim Sci, Wuhan 430070, Hubei, Peoples R China
[2] Huazhong Agr Univ, Coll Anim Sci, Key Lab Agr Anim Genet Breeding & Reprod, Minist Educ, Wuhan 430070, Hubei, Peoples R China
[3] Huazhong Agr Univ, Cooperat Innovat Ctr Sustainable Pig Prod, Wuhan 430070, Hubei, Peoples R China
来源
BMC MOLECULAR BIOLOGY | 2016年 / 17卷
关键词
miR-433; SMG5; NMD; PREMATURE TRANSLATIONAL TERMINATION; SMG5-SMG7; HETERODIMER; EMBRYONIC-DEVELOPMENT; GENE-EXPRESSION; STEM-CELL; UPF1; NMD; PROTEIN; SURVEILLANCE; DEGRADATION;
D O I
10.1186/s12867-016-0070-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: 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. Results: 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. Conclusions: 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.
引用
收藏
页数:8
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