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Loss of RPA1 induces Chk2 phosphorylation through a caffeine-sensitive pathway.

Araya R, Hirai I, Meyerkord CL, Wang HG

Drug Discovery Program, H. Lee Moffitt Cancer Center and Research Institute 12902 Magnolia Drive, Tampa, FL 33612, USA.

RPA is an important component of DNA replication, repair and recombination, but its involvement in the signaling of cell-cycle checkpoints is not well understood. In this study, we show that knockdown of RPA1 by siRNA duplexes induces ATM (Ser1981) and Chk2 (Thr68), but not Chk1 (Ser345) phosphorylation and results in p21 upregulation in HeLa cells. However, the induction of Chk2 (Thr68) phosphorylation and p21 expression by RPA1 siRNA transfection can be completely blocked by the ATM inhibitor caffeine. Moreover, transfection of siRNAs targeting ATM dramatically reduces Chk2 (Thr68) phosphorylation in RPA1 knockdown cells. Taken together, these results suggest that loss of RPA1 activates the Chk2 signaling pathway in an ATM-dependent manner.

Published 28 December 2004 in FEBS Lett, 579(1): 157-61.
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