DICER-dependent biogenesis of let-7 miRNAs affects human cell response to DNA damage via targeting p21/p27

Author:

Liu Bailong12,Liu Min12,Wang Jian2,Zhang Xiangming2,Wang Xiang2,Wang Ping2,Wang Hongyan2,Li Wei3,Wang Ya2

Affiliation:

1. Department of Radiation Oncology, The First Hospital of Jilin University, Changchun 130021, China

2. Department of Radiation Oncology, Emory University School of Medicine and Winship Cancer Institute, Atlanta, GA 30322, USA

3. Department of Cancer Center, The First Hospital of Jilin University, Changchun 130021, China

Abstract

Abstract Recently, it was reported that knockdown of DICER reduced the ATM-dependent DNA damage response and homologous recombination repair (HRR) via decreasing DICER-generated small RNAs at the damage sites. However, we found that knockdown of DICER dramatically increased cell resistance to camptothecin that induced damage required ATM to facilitate HRR. This phenotype is due to a prolonged G1/S transition via decreasing DICER-dependent biogenesis of miRNA let-7, which increased the p21Waf1/Cip1/p27Kip1 levels and resulted in decreasing the HRR efficiency. These results uncover a novel function of DICER in regulating the cell cycle through miRNA biogenesis, thus affecting cell response to DNA damage.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Genetics

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