The chromatin remodeler RSF1 coordinates epigenetic marks for transcriptional repression and DSB repair

Sunwoo Min, Ho Soo Lee, Jae Hoon Ji, Yungyeong Heo, Yonghyeon Kim, Sunyoung Chae, Yong Won Choi, Ho Chul Kang, Makoto Nakanishi, Hyeseong Cho

Resultado de la investigación: Articlerevisión exhaustiva

2 Citas (Scopus)

Resumen

DNA lesions impact on local transcription and the damage-induced transcriptional repression facilitates efficient DNA repair. However, how chromatin dynamics cooperates with these two events remained largely unknown. We here show that histone H2A acetylation at K118 is enriched in transcriptionally active regions. Under DNA damage, the RSF1 chromatin remodeling factor recruits HDAC1 to DSB sites. The RSF1-HDAC1 complex induces the deacetylation of H2A(X)-K118 and its deacetylation is indispensable for the ubiquitination of histone H2A at K119. Accordingly, the acetylation mimetic H2A-K118Q suppressed the H2A-K119ub level, perturbing the transcriptional repression at DNA lesions. Intriguingly, deacetylation of H2AX at K118 also licenses the propagation of γH2AX and recruitment of MDC1. Consequently, the H2AX-K118Q limits DNA repair. Together, the RSF1-HDAC1 complex controls the traffic of the DNA damage response and transcription simultaneously in transcriptionally active chromatins. The interplay between chromatin remodelers and histone modifiers highlights the importance of chromatin versatility in the maintenance of genome integrity.

Idioma originalEnglish (US)
Páginas (desde-hasta)12268-12283
Número de páginas16
PublicaciónNucleic acids research
Volumen49
N.º21
DOI
EstadoPublished - dic. 2 2021

ASJC Scopus subject areas

  • Genetics

Huella

Profundice en los temas de investigación de 'The chromatin remodeler RSF1 coordinates epigenetic marks for transcriptional repression and DSB repair'. En conjunto forman una huella única.

Citar esto