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PMID: 2574633 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

An essential G1 function for cyclin-like proteins in yeast.

Cell ·Vol. 59 ·No. 6 ·1989-12-22 ·Pages 1127-33

Richardson HE, Wittenberg C, Cross F, Reed SI

Abstract

Cyclins were discovered in marine invertebrates based on their dramatic cell cycle periodicity. Recently, the products of three genes associated with cell cycle progression in S. cerevisiae were found to share limited homology with cyclins. Mutational elimination of the CLN1, CLN2, and DAF1/WHI1 products leads to cell cycle arrest independent of cell type, while expression of any one of the genes allows cell proliferation. Using strains where CLN1 was expressed conditionally, the essential function of Cln proteins was found to be limited to the G1 phase. Furthermore, the ability of the Cln proteins to carry out this function was found to decay rapidly upon cessation of Cln biosynthesis. The data are consistent with the hypothesis that Cln proteins activate the Cdc28 protein kinase, shown to be essential for the G1 to S phase transition in S. cerevisiae. Because of the apparent functional redundancy of these genes, DAF1/WHI1 has been renamed CLN3.

MeSH Terms
Alleles Cell Cycle Chromosome Deletion DNA, Recombinant/metabolism Fungal Proteins/genetics,metabolism Genes, Fungal Interphase Kinetics Mutation Nuclear Proteins/genetics,metabolism Plasmids Proliferating Cell Nuclear Antigen Saccharomyces cerevisiae/cytology,genetics,growth & development Species Specificity Transformation, Genetic
Chemicals
DNA, Recombinant Fungal Proteins Nuclear Proteins Proliferating Cell Nuclear Antigen
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Richardson H E
Department of Molecular Biology, Research Institute of Scripps Clinic, La Jolla, California 92037.
Wittenberg C
Cross F
Reed S I
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1989-12-22
Pages
1127-33
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NIGMS NIH HHS · GM26176 · United States
NIGMS NIH HHS · GM38328 · United States
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