| Literature DB >> 32962915 |
Jenny Kaur Singh1, Haico van Attikum2.
Abstract
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.Entities:
Keywords: DNA double-strand break (DSB); DSB repair; Genome stability; Homologous recombination (HR); Non-homologous end joining (NHEJ); Zinc-finger (ZnF) proteins
Mesh:
Year: 2020 PMID: 32962915 DOI: 10.1016/j.semcdb.2020.09.003
Source DB: PubMed Journal: Semin Cell Dev Biol ISSN: 1084-9521 Impact factor: 7.727