Nucleic Acids Research Advance Access originally published online on August 13, 2008
Nucleic Acids Research 2008 36(16):5391-5404; doi:10.1093/nar/gkn522
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Nucleic Acids Research, 2008, Vol. 36, No. 16 5391-5404
© 2008 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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miR-16 family induces cell cycle arrest by regulating multiple cell cycle genes
Beijing Institute of Radiation Medicine, 27 Taiping Road, Beijing 100850, People's Republic of China
*To whom correspondence should be addressed. Fax: +86 10 68214653; Email: xfzheng100{at}126.com
Received March 25, 2008. Revised June 13, 2008. Accepted July 31, 2008.
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.
The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint First Authors.
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