Role of Cockayne Syndrome Group B Protein in Replication Stress: Implications for Cancer Therapy.

Abstract

A variety of endogenous and exogenous insults are capable of impeding replication fork progression, leading to replication stress. Several SNF2 fork remodelers have been shown to play critical roles in resolving this replication stress, utilizing different pathways dependent upon the nature of the DNA lesion, location on the DNA, and the stage of the cell cycle, to complete DNA replication in a manner preserving genetic integrity. Under certain conditions, however, the attempted repair may lead to additional genetic instability. Cockayne syndrome group B (CSB) protein, a SNF2 chromatin remodeler best known for its role in transcription-coupled nucleotide excision repair, has recently been shown to catalyze fork reversal, a pathway that can provide stability of stalled forks and allow resumption of DNA synthesis without chromosome breakage. Prolonged stalling of replication forks may collapse to give rise to DNA double-strand breaks, which are preferentially repaired by homology-directed recombination. CSB plays a role in repairing collapsed forks by promoting break-induced replication in S phase and early mitosis. In this review, we discuss roles of CSB in regulating the sources of replication stress, replication stress response, as well as the implications of CSB for cancer therapy.

• Authors: John R Walker, Xu-Dong Zhu
• Journal: International journal of molecular sciences (Int J Mol Sci) Vol. 23 Issue 18 (Sep 06 2022) ISSN: 1422-0067 [Electronic] Switzerland
• PMID: 36142121 (Publication Type: Journal Article, Review)

Chemical References

• Chromatin
• DNA-Binding Proteins
• DNA

Topics

• Chromatin
• Cockayne Syndrome (genetics)
• DNA (metabolism)
• DNA Repair
• DNA Replication
• DNA-Binding Proteins (metabolism)
• Humans
• Neoplasms (genetics, therapy)