The kinetochore protein Ndc10p is required for spindle stability and cytokinesis in yeast

Proc Natl Acad Sci U S A. 2005 Apr 12;102(15):5408-13. doi: 10.1073/pnas.0405925102. Epub 2005 Apr 4.

Abstract

The budding yeast kinetochore is comprised of >60 proteins and associates with 120 bp of centromeric (CEN) DNA. Kinetochore proteins are highly dynamic and exhibit programmed cell cycle changes in localization. The CEN-specific histone, Cse4p, is one of a few stable kinetochore components and remains associated with CEN DNA throughout mitosis. In contrast, several other kinetochore proteins have been observed along interpolar microtubules and at the midzone during anaphase. The inner kinetochore protein, Ndc10p, is enriched at the spindle midzone in late anaphase. We show that Ndc10p is transported to the plus-ends of interpolar microtubules at the midzone during anaphase, a process that requires survivin (Bir1p), a member of the aurora kinase (Ipl1p) complex, and Cdc14p phosphatase. In addition, Ndc10p is required for essential non-kinetochore processes during mitosis. Cells lacking functional Ndc10p show defects in spindle stability during anaphase and failure to split the septin ring during cytokinesis. This latter phenotype leads to a cell separation defect in ndc10-1 cells. We propose that Ndc10p plays a direct role in maintaining spindle stability during anaphase and coordinates the completion of cell division after chromosome segregation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Anaphase
  • Cell Cycle
  • Cell Cycle Proteins / metabolism
  • Cytokinesis*
  • DNA-Binding Proteins / metabolism*
  • Fungal Proteins / metabolism
  • Kinetochores / chemistry*
  • Kinetochores / metabolism
  • Microtubules / chemistry
  • Microtubules / metabolism
  • Protein Transport
  • Protein Tyrosine Phosphatases / metabolism
  • Saccharomyces cerevisiae / cytology*
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Spindle Apparatus / chemistry*
  • Spindle Apparatus / metabolism*

Substances

  • CBF2 protein, S cerevisiae
  • CDC14 protein, S cerevisiae
  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • Fungal Proteins
  • Saccharomyces cerevisiae Proteins
  • Protein Tyrosine Phosphatases