miR-16 family induces cell cycle arrest by regulating multiple cell cycle genes

被引:394
作者
Liu, Qin [1 ]
Fu, Hanjiang [1 ]
Sun, Fang [1 ]
Zhang, Haoming [1 ]
Tie, Yi [1 ]
Zhu, Jie [1 ]
Xing, Ruiyun [1 ]
Sun, Zhixian [1 ]
Zheng, Xiaofei [1 ]
机构
[1] Beijing Inst Radiat Med, Beijing 100850, Peoples R China
基金
北京市自然科学基金;
关键词
D O I
10.1093/nar/gkn522
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
MicroRNAs (miRNAs) are a class of small regulatory RNAs that are thought to be involved in diverse biological processes by regulating gene expression. Numerous miRNAs have been identified in various species, and many more miRNAs remain to be detected. Generally, hundreds of mRNAs have been predicted to be potential targets of one miRNA, so it is a great challenge to identify the genuine miRNA targets. Here, we generated the cell lines depleted of Drosha protein and screened dozens of transcripts (including Cyclin D1) regulated potentially by miRNA-mediated RNA silencing pathway. On the basis of miRNA expressing library, we established a miRNA targets reverse screening method by using luciferase reporter assay. By this method, we found that the expression of Cyclin D1 (CCND1) was regulated by miR-16 family directly, and miR-16 induced G1 arrest in A549 cells partially by CCND1. Furthermore, several other cell cycle genes were revealed to be regulated by miR-16 family, including Cyclin D3 (CCND3), Cyclin E1 (CCNE1) and CDK6. Taken together, our data suggests that miR-16 family triggers an accumulation of cells in G0/G1 by silencing multiple cell cycle genes simultaneously, rather than the individual target.
引用
收藏
页码:5391 / 5404
页数:14
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