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

机译:Let-7 miRNA的DICER依赖性生物发生通过靶向p21 / p27影响人类细胞对DNA损伤的反应

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摘要

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 p21(Waf1/Cip1)/p27(Kip1) 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.
机译:最近,有报道说,DICER的敲低通过减少损伤部位DICER产生的小RNA减少了ATM依赖性DNA损伤反应和同源重组修复(HRR)。但是,我们发现敲除DICER可以显着增加细胞对喜树碱的耐药性,而喜树碱诱导的损伤需要ATM才能促进HRR。此表型是由于通过减少miRNA let-7的DICER依赖性生物发生而延长了G1 / S过渡,从而增加了p21(Waf1 / Cip1)/ p27(Kip1)的水平,并导致HRR效率降低。这些结果揭示了DICER在通过miRNA生物发生调节细胞周期中的新功能,从而影响细胞对DNA损伤的反应。

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