生物
基因组不稳定性
DNA修复
核酸外切酶
端粒
核酸酶
细胞生物学
DNA复制
DNA损伤
遗传学
核苷酸切除修复
DNA
复制蛋白A
DNA错配修复
计算生物学
DNA结合蛋白
基因
DNA聚合酶
转录因子
作者
Sarah Sertic,Roberto Quadri,Federico Lazzaro,Marco Muzi-Falconi
出处
期刊:DNA Repair
[Elsevier]
日期:2020-09-01
卷期号:93: 102929-102929
被引量:34
标识
DOI:10.1016/j.dnarep.2020.102929
摘要
Exonuclease 1 (EXO1) is an evolutionarily well conserved exonuclease. Its ability to resect DNA in the 5′-3′ direction has been extensively characterized and shown to be implicated in several genomic DNA metabolic processes such as replication stress response, double strand break repair, mismatch repair, nucleotide excision repair and telomere maintenance. While the processing of DNA is critical for its repair, an excessive nucleolytic activity can lead to secondary lesions, increased genome instability and alterations in cellular functions. It is thus clear that different regulatory layers must be in effect to keep DNA degradation under control. Regulatory events that modulate EXO1 activity have been reported to act at different levels. Here we summarize the different post-translational modifications (PTMs) that affect EXO1 and discuss the implications of PTMs for EXO1 activities and how this regulation may be associated to cancer development.
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