CS proteins and ubiquitination: orchestrating DNA repair with transcription and cell division.

Trends Cell Biol

Faculty of Biomedical Sciences, Institute of Oncology Research, USI, Bellinzona 6500, Switzerland; Department of Functional Genomics and Cancer, IGBMC, CNRS/INSERM/University of Strasbourg, Illkirch-Graffenstaden 67400, Strasbourg, France; College of Medicine, Centre for Genomics and Precision Medicine, National Taiwan University, Taipei City, Taiwan.

Published: October 2024

AI Article Synopsis

  • Eukaryotic cells have developed sophisticated mechanisms to manage genotoxic stress, which is damage to DNA.
  • Cockayne syndrome (CS) is a rare disease caused by mutations in the CSA and CSB genes, initially thought to be solely responsible for DNA repair.
  • Recent findings reveal that CSA and CSB are crucial regulators that coordinate DNA repair, transcription, and cell division by ubiquitinating target proteins, highlighting the role of these proteins in the complex nature of CS.

Article Abstract

To face genotoxic stress, eukaryotic cells evolved extremely refined mechanisms. Defects in counteracting the threat imposed by DNA damage underlie the rare disease Cockayne syndrome (CS), which arises from mutations in the CSA and CSB genes. Although initially defined as DNA repair proteins, recent work shows that CSA and CSB act instead as master regulators of the integrated response to genomic stress by coordinating DNA repair with transcription and cell division. CSA and CSB exert this function through the ubiquitination of target proteins, which are effectors/regulators of these processes. This review describes how the ubiquitination of target substrates is a common denominator by which CSA and CSB participate in different aspects of cellular life and how their mutation gives rise to the complex disease CS.

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http://dx.doi.org/10.1016/j.tcb.2024.06.002DOI Listing

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