DNA Damage Triggers the Nuclear Accumulation of RASSF6 Tumor Suppressor Protein via CDK9 and BAF53 To Regulate p53 Target Gene Transcription

RASSF6, a member of the tumor suppressor Ras-association domain family (RASSF) proteins, regulates cell cycle arrest and apoptosis via p53 and plays a tumor suppressor role. We previously reported that RASSF6 blocks MDM2-mediated p53 degradation and enhances p53 expression. In this study, we demonst...

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Published inMolecular and cellular biology Vol. 42; no. 2; p. e0031021
Main Authors Kuleape, Joshua Agbemefa, Hossain, Shakhawoat, Sinclear, Caleb Kwame, Shimizu, Takanobu, Iwasa, Hiroaki, Maruyama, Junichi, Arimoto-Matsuzaki, Kyoko, Nishina, Hiroshi, Hata, Yutaka
Format Journal Article
LanguageEnglish
Published United States Taylor & Francis 01.02.2022
American Society for Microbiology
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Summary:RASSF6, a member of the tumor suppressor Ras-association domain family (RASSF) proteins, regulates cell cycle arrest and apoptosis via p53 and plays a tumor suppressor role. We previously reported that RASSF6 blocks MDM2-mediated p53 degradation and enhances p53 expression. In this study, we demonstrated that RASSF6 has nuclear localization and nuclear export signals and that DNA damage triggers the nuclear accumulation of RASSF6. We found that RASSF6 directly binds to BAF53, the component of SWI/SNF complex. DNA damage induces CDK9-mediated phosphorylation of BAF53, which enhances the interaction with RASSF6 and increases the amount of RASSF6 in the nucleus. Subsequently, RASSF6 augments the interaction between BAF53 and BAF60a, another component of the SWI/SNF complex, and further promotes the interaction of BAF53 and BAF60a with p53. BAF53 silencing or BAF60a silencing attenuates RASSF6-mediated p53 target gene transcription and apoptosis. Thus, RASSF6 is involved in the regulation of DNA damage-induced complex formation, including BAF53, BAF60a, and p53.
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The authors declare no conflict of interest.
ISSN:0270-7306
1098-5549
1098-5549
DOI:10.1128/mcb.00310-21