期刊
DNA REPAIR
卷 10, 期 12, 页码 1243-1251出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.dnarep.2011.09.013
关键词
Smt3; Ubiquitin; Protein modification; Protein degradation
资金
- National Science Foundation [MCB-0820228]
- NIH [GM081601]
- MRC [G0301154, G0400113] Funding Source: UKRI
- Cancer Research UK [12340] Funding Source: researchfish
- Medical Research Council [G0400113, G0301154] Funding Source: researchfish
- Div Of Molecular and Cellular Bioscience
- Direct For Biological Sciences [0820228] Funding Source: National Science Foundation
The two Siz/PIAS SUMO E3 ligases Siz1 and Siz2 are responsible for the vast majority of sumoylation in Saccharomyces cerevisiae. We found that siz1 Delta siz2 Delta mutants are sensitive to ultra-violet (UV) light. Epistasis analysis showed that the SIZ genes act in the nucleotide excision repair (NER) pathway, and suggested that they participate both in global genome repair (GGR) and in the Rpb9-dependent subpathway of transcription-coupled repair (TCR), but have minimal role in Rad26-dependent TCR. Quantitative analysis of NER at the single-nucleotide level showed that siz1 Delta siz2 Delta is deficient in repair of both the transcribed and non-transcribed strands of the DNA. These experiments confirmed that the SIZ genes participate in GGR. Their role in TCR remains unclear. It has been reported previously that mutants deficient for the SUMO conjugating enzyme Ubc9 contain reduced levels of Rad4, the yeast homolog of human XPC. However, our experiments do not support the conclusion that SUMO conjugation affects Rad4 levels. We found that several factors that participate in NER are sumoylated, including Rad4, Rad16, Rad7, Rad1, Rad10, Ssl2, Rad3, and Rpb4. Although Rad16 was heavily sumoylated, elimination of the major SUMO attachment sites in Rad16 had no detectable effect on UV resistance or removal of DNA lesions. SUMO attachment to most of these NER factors was significantly increased by DNA damage. Furthermore, SUMO-modified Rad4 accumulated in NER mutants that block the pathway downstream of Rad4, suggesting that SUMO becomes attached to Rad4 at a specific point during its functional cycle. Collectively, these results suggest that SIZ-dependent sumoylation may modulate the activity of multiple proteins to promote efficient NER. (C) 2011 Elsevier B.V. All rights reserved.
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