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Pellino1 regulates reversible ATM activation via NBS1 ubiquitination at DNA double-strand breaks.


ABSTRACT: DNA double-strand break (DSB) signaling and repair are critical for genome integrity. They rely on highly coordinated processes including posttranslational modifications of proteins. Here we show that Pellino1 (Peli1) is a DSB-responsive ubiquitin ligase required for the accumulation of DNA damage response proteins and efficient homologous recombination (HR) repair. Peli1 is activated by ATM-mediated phosphorylation. It is recruited to DSB sites in ATM- and γH2AX-dependent manners. Interaction of Peli1 with phosphorylated histone H2AX enables it to bind to and mediate the formation of K63-linked ubiquitination of NBS1, which subsequently results in feedback activation of ATM and promotes HR repair. Collectively, these results provide a DSB-responsive factor underlying the connection between ATM kinase and DSB-induced ubiquitination.

SUBMITTER: Ha GH 

PROVIDER: S-EPMC6450972 | biostudies-literature | 2019 Apr

REPOSITORIES: biostudies-literature

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Pellino1 regulates reversible ATM activation via NBS1 ubiquitination at DNA double-strand breaks.

Ha Geun-Hyoung GH   Ji Jae-Hoon JH   Chae Sunyoung S   Park Jihyun J   Kim Suhyeon S   Lee Jin-Kwan JK   Kim Yonghyeon Y   Min Sunwoo S   Park Jeong-Min JM   Kang Tae-Hong TH   Lee Ho H   Cho Hyeseong H   Lee Chang-Woo CW  

Nature communications 20190405 1


DNA double-strand break (DSB) signaling and repair are critical for genome integrity. They rely on highly coordinated processes including posttranslational modifications of proteins. Here we show that Pellino1 (Peli1) is a DSB-responsive ubiquitin ligase required for the accumulation of DNA damage response proteins and efficient homologous recombination (HR) repair. Peli1 is activated by ATM-mediated phosphorylation. It is recruited to DSB sites in ATM- and γH2AX-dependent manners. Interaction o  ...[more]

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