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Molecular and Cellular Biology
Article . 1997 . Peer-reviewed
License: ASM Journals Non-Commercial TDM
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Stimulation of Yeast Meiotic Gene Expression by the Glucose-Repressible Protein Kinase Rim15p

Authors: S, Vidan; A P, Mitchell;

Stimulation of Yeast Meiotic Gene Expression by the Glucose-Repressible Protein Kinase Rim15p

Abstract

The Saccharomyces cerevisiae RIM15 gene was identified previously through a mutation that caused reduced ability to undergo meiosis. We report here an analysis of the cloned RIM15 gene, which specifies a 1,770-residue polypeptide with homology to serine/threonine protein kinases. Rim15p is most closely related to Schizosaccharomyces pombe cek1+. Analysis of epitope-tagged derivatives indicates that Rim15p has autophosphorylation activity. Deletion of RIM15 causes reduced expression of several early meiotic genes (IME2, SPO13, and HOP1) and of IME1, which specifies an activator of early meiotic genes. However, overexpression of IME1 does not permit full expression of early meiotic genes in a rim15delta mutant. Ime1p activates early meiotic genes through its interaction with Ume6p, and analysis of Rim15p-dependent regulatory sites at the IME2 promoter indicates that activation through Ume6p is defective. Two-hybrid interaction assays suggest that Ime1p-Ume6p interaction is diminished in a rim15 mutant. Glucose inhibits Ime1p-Ume6p interaction, and we find that Rim15p accumulation is repressed in glucose-grown cells. Thus, glucose repression of Rim15p may be responsible for glucose inhibition of Ime1p-Ume6p interaction.

Related Organizations
Keywords

Mitogen-Activated Protein Kinase 3, Saccharomyces cerevisiae Proteins, Intracellular Signaling Peptides and Proteins, Nuclear Proteins, Cell Cycle Proteins, Saccharomyces cerevisiae, Protein Serine-Threonine Kinases, Protein-Tyrosine Kinases, Gene Expression Regulation, Enzymologic, DNA-Binding Proteins, Fungal Proteins, Repressor Proteins, Meiosis, Mutagenesis, Schizosaccharomyces, Mitogen-Activated Protein Kinases, Phosphorylation, Protein Kinases, Sequence Deletion, Transcription Factors

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    selected citations
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    109
    popularity
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    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
109
Top 10%
Top 10%
Top 10%
bronze