The BAH domain of BAF180 is required for PCNA ubiquitination

Atsuko Niimi, Suzanna R. Hopkins, Jessica A. Downs, Chikahide Masutani

研究成果: Article査読

13 被引用数 (Scopus)

抄録

Monoubiquitination of proliferating cell nuclear antigen (PCNA) is a critical regulator of post replication repair (PRR). The depletion of BAF180, a unique subunit of the PBAF chromatin remodeling complex in human cells results in reduced PCNA ubiquitination leading to less efficient fork progression following DNA damage, but little is known about the mechanism. Here, we report that the expression of exogenous BAF180 in cells promotes PCNA ubiquitination during S-phase after UV irradiation and it persists for many hours. No correlation was observed between the protein level of ubiquitin-specific protease 1 (USP1) and ubiquitinated PCNA in BAF180 expressing cells. Analysis of cells expressing BAF180 deletion mutants showed that the bromo-adjacent homology (BAH) domains are responsible for this effect. Surprisingly, a deletion construct encoding only the BAH domain region is able to increase the level of ubiquitinated PCNA, even though it is unable to be assembled into the PBAF complex. These results suggest that the ATPase-dependent chromatin remodeling activity of PBAF is not necessary, but instead the BAH domains are sufficient to promote PCNA ubiquitination.

本文言語English
ページ(範囲)16-23
ページ数8
ジャーナルMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
779
DOI
出版ステータスPublished - 01-09-2015
外部発表はい

All Science Journal Classification (ASJC) codes

  • 分子生物学
  • 遺伝学
  • 健康、毒物学および変異誘発

フィンガープリント

「The BAH domain of BAF180 is required for PCNA ubiquitination」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル