The SUMO-targeted ubiquitin ligase RNF4 localizes to etoposide-exposed mitotic chromosomes: implication for a novel DNA damage response during mitosis

Biochem Biophys Res Commun. 2014 Apr 25;447(1):83-8. doi: 10.1016/j.bbrc.2014.03.106. Epub 2014 Mar 30.

Abstract

RNF4, a SUMO-targeted ubiquitin ligase (STUbL), localizes to the nucleus and functions in the DNA damage response during interphase of the cell cycle. RNF4 also exists in cells undergoing mitosis, where its regulation and function remain poorly understood. Here we showed that administration of etoposide, an anticancer DNA topoisomerase II poison, to mitotic human cervical cancer HeLa cells induced SUMO-2/3-dependent localization of RNF4 to chromosomes. The FK2 antibody signals, indicative of poly/multi-ubiquitin assembly, were detected on etoposide-exposed mitotic chromosomes, whereas the signals were negligible in cells depleted for RNF4 by RNA interference. This suggests that RNF4 functions as a STUbL in the etoposide-induced damage response during mitosis. Indeed, RNF4-depletion sensitized mitotic HeLa cells to etoposide and increased cells with micronuclei. These results indicate the importance of the RNF4-mediated STUbL pathway during mitosis for the maintenance of chromosome integrity and further implicate RNF4 as a target for topo II poison-based therapy for cancer patients.

Keywords: Chromosome; DNA topoisomerase II; Etoposide (VP-16); Mitosis; Ring finger protein 4 (RNF4); Small ubiquitin-related modifier (SUMO)-targeted ubiquitin ligase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromosomes, Human / metabolism*
  • DNA Repair
  • DNA Topoisomerases, Type II
  • Etoposide / pharmacology*
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Mice
  • Micronuclei, Chromosome-Defective / chemically induced
  • Mitosis
  • Nuclear Proteins / drug effects
  • Nuclear Proteins / immunology
  • Nuclear Proteins / metabolism*
  • SUMO-1 Protein / immunology
  • Small Ubiquitin-Related Modifier Proteins / immunology
  • Transcription Factors / drug effects
  • Transcription Factors / immunology
  • Transcription Factors / metabolism*

Substances

  • Nuclear Proteins
  • RNF4 protein, human
  • SUMO-1 Protein
  • SUMO2 protein, human
  • Small Ubiquitin-Related Modifier Proteins
  • Transcription Factors
  • Etoposide
  • DNA Topoisomerases, Type II