Genome integrity is constantly challenged by various DNA lesions with DNA double-strand breaks (DSBs) as the most cytotoxic lesions. In order to faithfully repair DSBs, DNA damage response (DDR) signaling networks have evolved, which organize many multi-protein complexes to deal with the encountered DNA damage. Spatiotemporal dynamics of these protein complexes at DSBs are mainly modulated by post-translational modifications (PTMs). One of the most well-studied PTMs in DDR is ubiquitylation which can orchestrate cellular responses to DSBs, promote accurate DNA repair, and maintain genome integrity. Here, we summarize the recent advances of ubiquitin-dependent signaling in DDR and discuss how ubiquitylation crosstalks with other PTMs to control fundamental biological processes in DSB repair.
机构:
Columbia Univ, Inst Canc Genet, Med Ctr, New York, NY 10027 USA
Columbia Univ, Dept Genet & Dev, Med Ctr, New York, NY USAColumbia Univ, Inst Canc Genet, Med Ctr, New York, NY 10027 USA
Aparicio, Tomas
Baer, Richard
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Columbia Univ, Inst Canc Genet, Med Ctr, New York, NY 10027 USA
Columbia Univ, Dept Pathol & Cell Biol, Med Ctr, New York, NY USAColumbia Univ, Inst Canc Genet, Med Ctr, New York, NY 10027 USA
机构:
Capital Normal Univ, Beijing Key Lab DNA Damage Response & Coll Life S, Beijing 100048, Peoples R ChinaCapital Normal Univ, Beijing Key Lab DNA Damage Response & Coll Life S, Beijing 100048, Peoples R China
Li, Jing
Xu, Xingzhi
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Capital Normal Univ, Beijing Key Lab DNA Damage Response & Coll Life S, Beijing 100048, Peoples R ChinaCapital Normal Univ, Beijing Key Lab DNA Damage Response & Coll Life S, Beijing 100048, Peoples R China