BRCA1 downregulates the kinase activity of Polo-like kinase 1 in response to replication stress.
Ontology highlight
ABSTRACT: In response to DNA damage or replication stress, proliferating cells are arrested at different cell cycle stages for DNA repair by downregulating the activity of both the cyclin-dependent kinases (CDKs) and other important cell cycle kinases, including Polo-like kinase 1 (PLK1) . The signaling pathway to inhibit CDKs is relatively well understood, and breast cancer gene 1 (BRCA1) and other DNA damage response (DDR) factors play a key role in this process. However, the DNA damage-induced inhibition of PLK1 is still largely a mystery. Here we show that DNA damage and replication stress stimulate the association between BRCA1 and PLK1. Most importantly, we demonstrate that BRCA1 downregulates the kinase activity of PLK1 by modulating the dynamic interactions of Aurora A, hBora, and PLK1. Toge
SUBMITTER: Zou J
PROVIDER: S-EPMC3755076 | biostudies-literature | 2013 Jul
REPOSITORIES: biostudies-literature
ACCESS DATA