RBMX: a regulator for maintenance and centromeric protection of sister chromatid cohesion

Cell Rep. 2012 Apr 19;1(4):299-308. doi: 10.1016/j.celrep.2012.02.005. Epub 2012 Mar 22.

Abstract

Cohesion is essential for the identification of sister chromatids and for the biorientation of chromosomes until their segregation. Here, we have demonstrated that an RNA-binding motif protein encoded on the X chromosome (RBMX) plays an essential role in chromosome morphogenesis through its association with chromatin, but not with RNA. Depletion of RBMX by RNA interference (RNAi) causes the loss of cohesin from the centromeric regions before anaphase, resulting in premature chromatid separation accompanied by delocalization of the shugoshin complex and outer kinetochore proteins. Cohesion defects caused by RBMX depletion can be detected as early as the G2 phase. Moreover, RBMX associates with the cohesin subunits, Scc1 and Smc3, and with the cohesion regulator, Wapl. RBMX is required for cohesion only in the presence of Wapl, suggesting that RBMX is an inhibitor of Wapl. We propose that RBMX is a cohesion regulator that maintains the proper cohesion of sister chromatids.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carrier Proteins / metabolism
  • Carrier Proteins / physiology
  • Cell Cycle Proteins / metabolism
  • Cell Cycle Proteins / physiology
  • Centromere / metabolism
  • Chondroitin Sulfate Proteoglycans / metabolism
  • Chondroitin Sulfate Proteoglycans / physiology
  • Chromatids / metabolism
  • Chromatids / physiology*
  • Chromosomal Proteins, Non-Histone / metabolism
  • Chromosomal Proteins, Non-Histone / physiology
  • DNA-Binding Proteins
  • G2 Phase
  • HeLa Cells
  • Heterogeneous-Nuclear Ribonucleoproteins / genetics
  • Heterogeneous-Nuclear Ribonucleoproteins / metabolism
  • Heterogeneous-Nuclear Ribonucleoproteins / physiology*
  • Humans
  • Nuclear Proteins / metabolism
  • Nuclear Proteins / physiology
  • Phosphoproteins / metabolism
  • Phosphoproteins / physiology
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins / physiology
  • RNA Interference

Substances

  • Carrier Proteins
  • Cell Cycle Proteins
  • Chondroitin Sulfate Proteoglycans
  • Chromosomal Proteins, Non-Histone
  • DNA-Binding Proteins
  • Heterogeneous-Nuclear Ribonucleoproteins
  • Nuclear Proteins
  • Phosphoproteins
  • Proto-Oncogene Proteins
  • RAD21 protein, human
  • RBMX protein, human
  • SMC3 protein, human
  • WAPL protein, human