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Rrp1, Rrp2 and Uls1-Yeast SWI2/SNF2 DNA dependent translocases in genome stability maintenance
被引:3
|作者:
Kramarz, Karol
[1
]
Dziadkowiec, Dorota
[2
]
机构:
[1] Univ Wroclaw, Fac Biol Sci, Acad Excellence Hub Res Ctr DNA Repair & Replicat, Wroclaw, Poland
[2] Univ Wroclaw, Fac Biotechnol, Wroclaw, Poland
来源:
关键词:
Yeast;
Replication stress;
DNA repair;
Translocase;
Ubiquitin ligase;
SUMOylation;
REPLICATION FORK REVERSAL;
CELL NUCLEAR ANTIGEN;
HOMOLOGOUS RECOMBINATION;
POSTREPLICATION REPAIR;
FISSION YEAST;
RAD51;
RECOMBINASE;
PROTEIN ULS1;
UBIQUITIN;
SUMO;
CHROMATIN;
D O I:
10.1016/j.dnarep.2022.103356
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Multiple eukaryotic SWI2/SNF2 DNA translocases safeguard genome integrity, mostly by remodelling nucleosomes, but also by fine-tuning mechanisms of DNA repair, such as homologous recombination. Among this large family there is a unique class of Rad5/16-like enzymes, including Saccharomyces cerevisiae Uls1 and its Schizosaccharomyces pombe orthologues Rrp1 and Rrp2, that have both translocase and E3 ubiquitin ligase activities, and are often directed towards their substrates by SUMOylation. Here we summarize recent advances in understanding how different activities of these yeast proteins jointly contribute to their important roles in replication stress response particularly at centromeres and telomeres. This extends the possible range of functions performed by this class of SNF2 enzymes in human cells involving both their translocase and ubiquitin ligase activities and related to SUMOylation pathways within the nucleus.
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