Plo1 kinase recruitment to the spindle pole body and its role in cell division in Schizosaccharomyces pombe

Mol Biol Cell. 1999 Aug;10(8):2771-85. doi: 10.1091/mbc.10.8.2771.

Abstract

Polo kinases execute multiple roles during cell division. The fission yeast polo related kinase Plo1 is required to assemble the mitotic spindle, the prophase actin ring that predicts the site for cytokinesis and for septation after the completion of mitosis (Ohkura et al., 1995; Bahler et al., 1998). We show that Plo1 associates with the mitotic but not interphase spindle pole body (SPB). SPB association of Plo1 is the earliest fission yeast mitotic event recorded to date. SPB association is strong from mitotic commitment to early anaphase B, after which the Plo1 signal becomes very weak and finally disappears upon spindle breakdown. SPB association of Plo1 requires mitosis-promoting factor (MPF) activity, whereas its disassociation requires the activity of the anaphase-promoting complex. The stf1.1 mutation bypasses the usual requirement for the MPF activator Cdc25 (Hudson et al., 1990). Significantly, Plo1 associates inappropriately with the interphase SPB of stf1.1 cells. These data are consistent with the emerging theme from many systems that polo kinases participate in the regulation of MPF to determine the timing of commitment to mitosis and may indicate that pole association is a key aspect of Plo1 function. Plo1 does not associate with the SPB when septation is inappropriately driven by deregulation of the Spg1 pathway and remains SPB associated if septation occurs in the presence of a spindle. Thus, neither Plo1 recruitment to nor its departure from the SPB are required for septation; however, overexpression of plo1+ activates the Spg1 pathway and causes transient Cdc7 recruitment to the SPB and multiple rounds of septation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anaphase-Promoting Complex-Cyclosome
  • Basic-Leucine Zipper Transcription Factors
  • CDC2 Protein Kinase / metabolism
  • Cell Cycle Proteins / metabolism
  • Cell Division / physiology
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Drosophila Proteins*
  • GTP Phosphohydrolases / metabolism
  • Interphase / physiology
  • Ligases / metabolism
  • Maturation-Promoting Factor / metabolism
  • Mitosis / physiology
  • Phosphoprotein Phosphatases / metabolism
  • Protein Serine-Threonine Kinases / metabolism*
  • Schizosaccharomyces / cytology
  • Schizosaccharomyces / metabolism*
  • Soybean Proteins*
  • Spindle Apparatus / metabolism*
  • Ubiquitin-Protein Ligase Complexes*
  • Ubiquitin-Protein Ligases
  • cdc25 Phosphatases

Substances

  • Basic-Leucine Zipper Transcription Factors
  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • Drosophila Proteins
  • STF1 protein, Glycine max
  • Soybean Proteins
  • Ubiquitin-Protein Ligase Complexes
  • Anaphase-Promoting Complex-Cyclosome
  • Ubiquitin-Protein Ligases
  • Protein Serine-Threonine Kinases
  • CDC2 Protein Kinase
  • Maturation-Promoting Factor
  • Phosphoprotein Phosphatases
  • cdc25 Phosphatases
  • GTP Phosphohydrolases
  • Ligases