Nucleolin is a histone chaperone with FACT-like activity and assists remodeling of nucleosomes

EMBO J. 2006 Apr 19;25(8):1669-79. doi: 10.1038/sj.emboj.7601046. Epub 2006 Apr 6.

Abstract

Remodeling machines play an essential role in the control of gene expression, but how their activity is regulated is not known. Here we report that the nuclear protein nucleolin possesses a histone chaperone activity and that this factor greatly enhances the activity of the chromatin remodeling machineries SWI/SNF and ACF. Interestingly, nucleolin is able to induce the remodeling by SWI/SNF of macroH2A, but not of H2ABbd nucleosomes, which are otherwise resistant to remodeling. This new histone chaperone promotes the destabilization of the histone octamer, helping the dissociation of a H2A-H2B dimer, and stimulates the SWI/SNF-mediated transfer of H2A-H2B dimers. Furthermore, nucleolin facilitates transcription through the nucleosome, which is reminiscent of the activity of the FACT complex. This work defines new functions for histone chaperones in chromatin remodeling and regulation of transcription and explains how nucleolin could act on transcription.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Chromatin Assembly and Disassembly*
  • Chromosomal Proteins, Non-Histone / metabolism
  • DNA-Binding Proteins / physiology*
  • Dimerization
  • High Mobility Group Proteins / physiology*
  • Histones / metabolism*
  • Humans
  • Nucleolin
  • Nucleosomes / metabolism
  • Nucleosomes / physiology*
  • Phosphoproteins / physiology*
  • Protein Transport
  • RNA Polymerase II / metabolism
  • RNA-Binding Proteins / physiology*
  • Transcription Factors / metabolism
  • Transcriptional Activation
  • Transcriptional Elongation Factors / physiology*
  • Xenopus laevis

Substances

  • Chromosomal Proteins, Non-Histone
  • DNA-Binding Proteins
  • High Mobility Group Proteins
  • Histones
  • Nucleosomes
  • Phosphoproteins
  • RNA-Binding Proteins
  • SSRP1 protein, human
  • SWI-SNF-B chromatin-remodeling complex
  • Transcription Factors
  • Transcriptional Elongation Factors
  • RNA Polymerase II