CDK2-dependent activation of PARP-1 is required for hormonal gene regulation in breast cancer cells.

ABSTRACT: Eukaryotic gene regulation implies that transcription factors gain access to genomic information via poorly understood processes involving activation and targeting of kinases, histone-modifying enzymes, and chromatin remodelers to chromatin. Here we report that progestin gene regulation in breast cancer cells requires a rapid and transient increase in poly-(ADP)-ribose (PAR), accompanied by a dramatic decrease of cellular NAD that could have broad implications in cell physiology. This rapid increase in nuclear PARylation is mediated by activation of PAR polymerase PARP-1 as a result of phosphorylation by cyclin-dependent kinase CDK2. Hormone-dependent phosphorylation of PARP-1 by CDK2, within the catalytic domain, enhances its enzymatic capabilities. Activated PARP-1 contributes to the dis

ORGANISM(S): Homo sapiens

SUBMITTER: Miguel Beato 

PROVIDER: E-GEOD-53855 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress