Rad21 is required for centrosome integrity in human cells independently of its role in chromosome cohesion

Cell Cycle. 2010 May;9(9):1774-80. doi: 10.4161/cc.9.9.11524. Epub 2010 May 15.

Abstract

Classically, chromosomal functions in DNA repair and sister chromatid association have been assigned to the cohesin proteins. More recent studies have provided evidence that cohesins also localize to the centrosomes, which organize the bipolar spindle during mitosis. Depletion of cohesin proteins is associated with multi-polar mitosis in which spindle pole integrity is compromised. However, the spindle pole defects after cohesin depletion could be an indirect consequence of a chromosomal cohesion defect which might impact centrosome integrity via alterations to the spindle microtubule network. Here we show that the cohesin Rad21 is required for centrosome integrity independently of its role as a chromosomal cohesin. Thus, Rad21 may promote accurate chromosome transmission not only by virtue of its function as a chromosomal cohesin, but also because it is required for centrosome function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Cycle Proteins / metabolism
  • Centrosome / metabolism*
  • Chromosomal Proteins, Non-Histone / metabolism
  • Chromosome Segregation
  • Cohesins
  • DNA-Binding Proteins
  • HeLa Cells
  • Humans
  • Interphase
  • Mitosis
  • Nuclear Proteins / metabolism*
  • Nuclear Proteins / physiology
  • Phosphoproteins / metabolism*
  • Phosphoproteins / physiology
  • Polo-Like Kinase 1
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins / metabolism
  • RNA Interference
  • RNA, Small Interfering / metabolism

Substances

  • Cell Cycle Proteins
  • Chromosomal Proteins, Non-Histone
  • DNA-Binding Proteins
  • Nuclear Proteins
  • Phosphoproteins
  • Proto-Oncogene Proteins
  • RAD21 protein, human
  • RNA, Small Interfering
  • Protein Serine-Threonine Kinases