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

被引:23
作者
Bouhlel, Imene B. [1 ,2 ]
Ohta, Midori [3 ]
Mayeux, Adeline [1 ,2 ]
Bordes, Nicole [1 ,2 ]
Dingli, Florent [1 ]
Boulanger, Jerome [1 ,2 ]
Casquillas, Guilhem Velve [1 ,2 ]
Loew, Damarys [1 ]
Tran, Phong T. [1 ,2 ]
Sato, Masamitsu [3 ]
Paoletti, Anne [1 ,2 ]
机构
[1] Ctr Rech, Inst Curie, F-75248 Paris, France
[2] CNRS, UMR144, F-75248 Paris, France
[3] Waseda Univ, Tokyo 1698050, Japan
关键词
Cell Cycle; Centrosome; Mitotic spindle; SPB; SACCHAROMYCES-CEREVISIAE; CENTROSOME AMPLIFICATION; SCHIZOSACCHAROMYCES-POMBE; CENTRIOLE SEPARATION; NUCLEAR-ENVELOPE; HALF-BRIDGE; BASAL BODY; KINASE; GENE; PROTEINS;
D O I
10.1242/jcs.159657
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:1481 / 1493
页数:13
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