Cell cycle control of spindle pole body duplication and splitting by Sfi1 and Cdc31 in fission yeast

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 Schizosacchar...

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Veröffentlicht in:Journal of cell science 2015-04, Vol.128 (8), p.1481-1493
Hauptverfasser: Bouhlel, Imène B, Ohta, Midori, Mayeux, Adeline, Bordes, Nicole, Dingli, Florent, Boulanger, Jérôme, Velve Casquillas, Guilhem, Loew, Damarys, Tran, Phong T, Sato, Masamitsu, Paoletti, Anne
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Sprache:eng
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Zusammenfassung: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.
ISSN:0021-9533
1477-9137
DOI:10.1242/jcs.159657