Regulation of the localization of Dbf2 and Mob1 during cell division of Saccharomyces cerevisiae

Satoshi Yoshida, A. Toh-e

Research output: Contribution to journalArticle

43 Citations (Scopus)

Abstract

The mitotic exit network (MEN) governs Cdk inactivation. In budding yeast, MEN consists of the protein phosphatase Cdc14, the ras-like GTPase Tem1, protein kinases Cdc15, Cdc5, Dbf2 and Dbf2-binding protein Mob1. Tem1, Dbf2, Cdc5 and Cdc15 have been reported to be localized at the spindle pole body (SPB). Here we report changes of the localization of Dbf2 and Mob1 during cell division. Dbf2 and Mob1 localize to the SPBs in anaphase and then moves to the bud neck, just prior to actin ring assembly, consistent with their role in cytokinesis. The neck localization, but not SPB localization, of Dbf2 was inhibited by the Bub2 spindle checkpoint. Cdc14 is the downstream target of Dbf2 in Cdk inactivation, but we found that the neck localization of Dbf2 and Mob1 was dependent on the Cdc14 activity, suggesting that Dbf2 and Mob1 function in cytokinesis at the end of the mitotic signaling cascade.

Original languageEnglish
Pages (from-to)141-147
Number of pages7
JournalGenes and Genetic Systems
Volume76
Issue number2
DOIs
Publication statusPublished - 2001 Jun 13
Externally publishedYes

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Spindle Pole Bodies
Cytokinesis
Cell Division
Saccharomyces cerevisiae
Neck
ras Proteins
Anaphase
Saccharomycetales
Phosphoprotein Phosphatases
Protein Kinases
Actins
Carrier Proteins

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics

Cite this

Regulation of the localization of Dbf2 and Mob1 during cell division of Saccharomyces cerevisiae. / Yoshida, Satoshi; Toh-e, A.

In: Genes and Genetic Systems, Vol. 76, No. 2, 13.06.2001, p. 141-147.

Research output: Contribution to journalArticle

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