DNA double-strand break repair: Putting zinc fingers on the sore spot

被引:30
|
作者
Singh, Jenny Kaur [1 ]
van Attikum, Haico [1 ]
机构
[1] Leiden Univ, Dept Human Genet, Med Ctr, Einthovenweg 20, NL-2333 ZC Leiden, Netherlands
基金
欧洲研究理事会; 荷兰研究理事会;
关键词
Zinc-finger (ZnF) proteins; DNA double-strand break (DSB); DSB repair; Non-homologous end joining (NHEJ); Homologous recombination (HR); Genome stability; HOMOLOGOUS-RECOMBINATION; DAMAGE RESPONSE; GENOME INTEGRITY; HISTONE DEMETHYLASE; UBIQUITIN-BINDING; CHROMATIN; PROTEIN; PROMOTES; RECRUITMENT; DOMAINS;
D O I
10.1016/j.semcdb.2020.09.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Zinc-Finger (ZnF) proteins represent one of the most abundant group of proteins in the human genome. At first characterized as DNA binding proteins, it has become increasingly clear that ZnF-proteins have the ability to bind a large variety of substrates such as RNAs, proteins and post-translational modifications, suggesting potential roles in a variety of biological processes. Indeed, several studies have implicated ZnF-proteins for instance in transcription regulation, signal transduction and cell migration. Intriguingly, more recently these proteins have emerged as important protectors of the genome, particularly by orchestrating the repair of highly deleterious DNA double-strand breaks. Here we provide a comprehensive summary of the roles of ZnF domain-containing proteins in DNA double-strand break repair and discuss how their dysfunction impacts genome stability and human disease.
引用
收藏
页码:65 / 74
页数:10
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