Systems-wide analysis of ubiquitylation dynamics reveals a key role for PAF15 ubiquitylation in DNA-damage bypass
Research output: Contribution to journal › Journal article › Research › peer-review
Protein ubiquitylation has emerged as a key regulatory mechanism in DNA-damage signalling and repair pathways. We report a proteome-wide, site-specific survey of ubiquitylation changes after ultraviolet irradiation, identifying numerous upregulated and downregulated ubiquitylation sites on known components of DNA-damage signalling, as well as on proteins not previously implicated in this process. Our results uncover a critical role for PCNA-associated factor PAF15 (p15(PAF)/KIAA0101) ubiquitylation during DNA replication. During unperturbed S phase, chromatin-associated PAF15 is modified by double mono-ubiquitylation of Lys 15 and 24 templated through PCNA binding. Replication blocks trigger rapid, proteasome-dependent removal of Lys 15/24-ubiquitylated PAF15 from PCNA, facilitating bypass of replication-fork-blocking lesions by allowing recruitment of translesion DNA synthesis polymerase polη to mono-ubiquitylated PCNA at stalled replisomes. Our findings demonstrate widespread involvement of ubiquitin signalling in genotoxic-stress responses and identify a critical function for dynamic PAF15 ubiquitylation in safeguarding genome integrity when DNA replication is challenged.
Original language | English |
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Journal | Nature Cell Biology |
Volume | 14 |
Issue number | 10 |
Pages (from-to) | 1089-98 |
Number of pages | 10 |
ISSN | 1465-7392 |
DOIs | |
Publication status | Published - Oct 2012 |
- Carrier Proteins, Cell Line, DNA Damage, DNA Repair, DNA Replication, DNA-Directed DNA Polymerase, Humans, Lysine, Proteasome Endopeptidase Complex, S Phase, Signal Transduction, Ubiquitination, Ultraviolet Rays
Research areas
ID: 46282763