HJURP involvement in de novo CenH3(CENP-A) and CENP-C recruitment

Cell Rep. 2015 Apr 7;11(1):22-32. doi: 10.1016/j.celrep.2015.03.013. Epub 2015 Apr 2.

Abstract

Although our understanding of centromere maintenance, marked by the histone H3 variant CenH3(CENP-A) in most eukaryotes, has progressed, the mechanism underlying the de novo formation of centromeres remains unclear. We used a synthetic system to dissect how CenH3(CENP-A) contributes to the accumulation of CENP-C and CENP-T, two key components that are necessary for the formation of functional kinetochores. We find that de novo CENP-T accumulation depends on CENP-C and that recruitment of these factors requires two domains in CenH3(CENP-A): the HJURP-binding region (CATD) and the CENP-C-binding region (CAC). Notably, HJURP interacts directly with CENP-C and is critical for de novo accumulation of CENP-C at synthetic centromeres. On the basis of our findings, we propose that HJURP serves a dual chaperone function in coordinating CenH3(CENP-A) and CENP-C recruitment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autoantigens / genetics*
  • Autoantigens / metabolism
  • Centromere / genetics
  • Centromere Protein A
  • Chromosomal Proteins, Non-Histone / genetics*
  • Chromosomal Proteins, Non-Histone / metabolism
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Histones / genetics
  • Humans
  • Kinetochores / metabolism
  • Molecular Chaperones / genetics
  • Nucleosomes / genetics
  • Protein Binding / genetics

Substances

  • Autoantigens
  • CENPA protein, human
  • CENPT protein, human
  • Centromere Protein A
  • Chromosomal Proteins, Non-Histone
  • DNA-Binding Proteins
  • HJURP protein, human
  • Histones
  • Molecular Chaperones
  • Nucleosomes
  • centromere protein C