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PMID: 15737064 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Shugoshin prevents dissociation of cohesin from centromeres during mitosis in vertebrate cells.

PLoS biology ·Vol. 3 ·No. 3 ·2005-03-00 ·Pages e86

McGuinness BE, Hirota T, Kudo NR, Peters JM, Nasmyth K

Abstract

Cohesion between sister chromatids is essential for their bi-orientation on mitotic spindles. It is mediated by a multisubunit complex called cohesin. In yeast, proteolytic cleavage of cohesin's alpha kleisin subunit at the onset of anaphase removes cohesin from both centromeres and chromosome arms and thus triggers sister chromatid separation. In animal cells, most cohesin is removed from chromosome arms during prophase via a separase-independent pathway involving phosphorylation of its Scc3-SA1/2 subunits. Cohesin at centromeres is refractory to this process and persists until metaphase, whereupon its alpha kleisin subunit is cleaved by separase, which is thought to trigger anaphase. What protects centromeric cohesin from the prophase pathway? Potential candidates are proteins, known as shugoshins, that are homologous to Drosophila MEI-S332 and yeast Sgo1 proteins, which prevent removal of meiotic cohesin complexes from centromeres at the first meiotic division. A vertebrate shugoshin-like protein associates with centromeres during prophase and disappears at the onset of anaphase. Its depletion by RNA interference causes HeLa cells to arrest in mitosis. Most chromosomes bi-orient on a metaphase plate, but precocious loss of centromeric cohesin from chromosomes is accompanied by loss of all sister chromatid cohesion, the departure of individual chromatids from the metaphase plate, and a permanent cell cycle arrest, presumably due to activation of the spindle checkpoint. Remarkably, expression of a version of Scc3-SA2 whose mitotic phosphorylation sites have been mutated to alanine alleviates the precocious loss of sister chromatid cohesion and the mitotic arrest of cells lacking shugoshin. These data suggest that shugoshin prevents phosphorylation of cohesin's Scc3-SA2 subunit at centromeres during mitosis. This ensures that cohesin persists at centromeres until activation of separase causes cleavage of its alpha kleisin subunit. Centromeric cohesion is one of the hallmarks of mitotic chromosomes. Our results imply that it is not an intrinsically stable property, because it can easily be destroyed by mitotic kinases, which are kept in check by shugoshin.

MeSH Terms
Amino Acid Sequence Anaphase/physiology Animals Base Sequence Cell Cycle Proteins/physiology Centromere/physiology Chromosomal Proteins, Non-Histone DNA Primers Fungal Proteins/physiology HeLa Cells Humans Mice Mitosis/physiology Molecular Sequence Data Nuclear Proteins/physiology Peptide Fragments/chemistry Proteins/chemistry,genetics RNA, Small Interfering/genetics Sister Chromatid Exchange
Chemicals
Cell Cycle Proteins Chromosomal Proteins, Non-Histone DNA Primers Fungal Proteins Nuclear Proteins Peptide Fragments Proteins RNA, Small Interfering SGO1 protein, human cohesins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
McGuinness Barry E
Research Institute of Molecular Pathology, Vienna, Austria.
Hirota Toru
Kudo Nobuaki R
Peters Jan-Michael
Nasmyth Kim
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Article Info
Journal
PLoS biology
Abbr.
PLoS Biol
ISSN
1545-7885
Published
2005-03-00
Epub
2005-00-01
Pages
e86
Language
English
Region
United States
NLM ID
101183755
PMCID
PMC1054882
Subset
IM
Databases
GENBANK
AB193056, AB193057, AB193058, AB193059, AB193060, AB193061, AB193062, AB193063, AB193064, AB193065, AB193066, AB193067, AB193068
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