Literature DB >> 15296722

Cdc28/Cdk1 regulates spindle pole body duplication through phosphorylation of Spc42 and Mps1.

Sue L Jaspersen1, Brenda J Huneycutt, Thomas H Giddings, Katheryn A Resing, Natalie G Ahn, Mark Winey.   

Abstract

Duplication of the Saccharomyces cerevisiae spindle pole body (SPB) once per cell cycle is essential for bipolar spindle formation and accurate chromosome segregation during mitosis. We have investigated the role that the major yeast cyclin-dependent kinase Cdc28/Cdk1 plays in assembly of a core SPB component, Spc42, to better understand how SPB duplication is coordinated with cell cycle progression. Cdc28 is required for SPB duplication and Spc42 assembly, and we found that Cdc28 directly phosphorylates Spc42 to promote its assembly into the SPB. The Mps1 kinase, previously shown to regulate Spc42 phosphorylation and assembly, is also a Cdc28 substrate, and Cdc28 phosphorylation of Mps1 is needed to maintain wild-type levels of Mps1 in cells. Analysis of nonphosphorylatable mutants in SPC42 and MPS1 indicates that direct Spc42 phosphorylation and indirect regulation of Spc42 through Mps1 are two overlapping pathways by which Cdc28 regulates Spc42 assembly and SPB duplication during the cell cycle.

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Year:  2004        PMID: 15296722     DOI: 10.1016/j.devcel.2004.07.006

Source DB:  PubMed          Journal:  Dev Cell        ISSN: 1534-5807            Impact factor:   12.270


  34 in total

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Journal:  Mol Biol Cell       Date:  2006-06-14       Impact factor: 4.138

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10.  Preventing the degradation of mps1 at centrosomes is sufficient to cause centrosome reduplication in human cells.

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