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PMID: 8816449 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Prenylated isoforms of yeast casein kinase I, including the novel Yck3p, suppress the gcs1 blockage of cell proliferation from stationary phase.

Molecular and cellular biology ·Vol. 16 ·No. 10 ·1996-10-00 ·Pages 5375-85

Wang X, Hoekstra MF, DeMaggio AJ, Dhillon N, Vancura A, Kuret J, Johnston GC, Singer RA

Abstract

The GCS1 gene of the budding yeast Saccharomyces cerevisiae mediate the resumption of cell proliferation from the starved, stationary-phase state. Here we identify yeast genes that, in increased dosages, overcome the growth defect of gcs1 delta mutant cells. Among these are YCK1 (CK12) and YCK2 (CKI1), encoding membrane-associated casein kinase I, and YCK3, encoding a novel casein kinase I isoform. Some Yck3p gene product was found associated with the plasma membrane, like Yck1p and Yck2p, but most confractionated with the nucleus, like another yeast casein kinase I isoform, Hrr25p. Genetic studies showed that YCK3 and HRR25 constitute an essential gene family and that Yck3p can weakly substitute for Yck1p-Yck2p. For gcs1 delta suppression, both a protein kinase domain and a C-terminal prenylation motif were shown to be necessary. An impairment in endocytosis was found for gcs1 delta mutant cells, which was alleviated by an increased YCK2 gene dosage. The ability of an increased casein kinase I gene dosage to suppress the effects caused by the absence of Gcs1p suggests that Gcs1p and Yck1p-Yck2p affect parallel pathways.

MeSH Terms
Amino Acid Sequence Animals Casein Kinase I Casein Kinases Cattle Cell Cycle Cell Division Genes, Fungal Genotype Isoenzymes/biosynthesis,chemistry,metabolism Models, Structural Molecular Sequence Data Mutagenesis Protein Kinase C/metabolism Protein Kinases/biosynthesis,chemistry,metabolism Protein Prenylation Protein Structure, Secondary Restriction Mapping Saccharomyces cerevisiae/cytology,growth & development,physiology Saccharomyces cerevisiae Proteins Sequence Homology, Amino Acid Suppression, Genetic
Chemicals
Isoenzymes Saccharomyces cerevisiae Proteins Protein Kinases Casein Kinase I Casein Kinases YCK1 protein, S cerevisiae YCK2 protein, S cerevisiae Protein Kinase C
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Wang X
Department of Biochemistry, Dalhousie University, Halifax, Nova Scotia, Canada.
Hoekstra M F
DeMaggio A J
Dhillon N
Vancura A
Kuret J
Johnston G C
Singer R A
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1996-10-00
Pages
5375-85
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC231536
Subset
IM
Grants
NIGMS NIH HHS · GM 48216 · United States
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