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

Authors:
Nicole A Beauchene Laura A Díaz-Martínez Katherine Furniss Wei-Shan Hsu Hung-Ji Tsai Chris Chamberlain Pedro Esponda Juan F Giménez-Abián Duncan J Clarke

Cell Cycle 2010 May 15;9(9):1774-80. Epub 2010 May 15.

Department of Genetics, Cell Biology & Development, University of Minnesota Medical School, Minneapolis, MN, USA.

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.

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http://dx.doi.org/10.4161/cc.9.9.11524DOI Listing
May 2010

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