Cell cycle control of spindle pole body duplication and splitting by Sfi1 and Cdc31 in fission yeast
Author(s) -
Imène Bouhlel,
Midori Ohta,
Adeline Mayeux,
Nicole Bordes,
Florent Dingli,
Jérôme Boulanger,
Guilhem Velvé Casquillas,
Damarys Loew,
Phong T. Tran,
Masamitsu Sato,
Anne Paoletti
Publication year - 2015
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.159657
Subject(s) - spindle pole body , biology , schizosaccharomyces pombe , microbiology and biotechnology , mitosis , anaphase , schizosaccharomyces , spindle apparatus , cyclin dependent kinase 1 , telophase , genetics , cell cycle , yeast , cell division , saccharomyces cerevisiae , cell
Spindle pole biogenesis and segregation are tightly coordinated to produce a bipolar mitotic spindle. In yeasts, the spindle pole body (SPB) half-bridge composed of Sfi1 and Cdc31 duplicates to promote the biogenesis of a second SPB. Sfi1 accumulates at the half-bridge in two phases in Schizosaccharomyces pombe, from anaphase to early septation and throughout G2 phase. We found that the function of Sfi1-Cdc31 in SPB duplication is accomplished before septation ends and G2 accumulation starts. Thus, Sfi1 early accumulation at mitotic exit might correspond to half-bridge duplication. We further show that Cdc31 phosphorylation on serine 15 in a Cdk1 (encoded by cdc2) consensus site is required for the dissociation of a significant pool of Sfi1 from the bridge and timely segregation of SPBs at mitotic onset. This suggests that the Cdc31 N-terminus modulates the stability of Sfi1-Cdc31 arrays in fission yeast, and impacts on the timing of establishment of spindle bipolarity.
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