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PMID: 3302675 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The ras-like yeast YPT1 gene is itself essential for growth, sporulation, and starvation response.

Molecular and cellular biology ·Vol. 7 ·No. 7 ·1987-07-00 ·Pages 2367-77

Segev N, Botstein D

Abstract

The Saccharomyces cerevisiae gene YPT1 encodes a protein that exhibits significant homology to the mammalian ras proteins. Using gene disruption techniques, we have shown that the intact YPT1 gene is required for spore viability. Lethality caused by loss of YPT1 function, unlike that caused by loss of the yeast ras homologs RAS1 and RAS2 function, is not suppressed by the bcy1 mutation, suggesting that YPT1 does not act through the adenylate cyclase regulatory system. A cold-sensitive allele, ypt1-1, was constructed. At the nonpermissive temperature, mutants died, exhibiting aberrant nuclear morphology, as well as abnormal distribution of actin and tubulin. The mutant cells died without exhibiting classical cell-cycle-specific arrest; nevertheless, examination of cellular DNA content suggests that the YPT1 function is required, particularly after S phase. Cells carrying the ypt1-1 mutation died upon nitrogen starvation even at a temperature permissive for growth; diploid cells homozygous for ypt1-1 did not sporulate. The YPT1 gene is thus involved in nutritional regulation of the cell cycle as well as in normal progression through the mitotic cell cycle.

MeSH Terms
Adenylyl Cyclases/genetics Cell Cycle Fungal Proteins/genetics Genes, Fungal Mutation Nitrogen/metabolism Oncogenes Phenotype Plasmids Saccharomyces cerevisiae/genetics,growth & development,physiology Spores, Fungal/genetics Transformation, Genetic
Chemicals
Fungal Proteins Adenylyl Cyclases Nitrogen
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Segev N
Botstein D
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46 references, click to expand
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1987-07-00
Pages
2367-77
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC365368
Subset
IM
Grants
NIGMS NIH HHS · GM 18973 · United States
NIGMS NIH HHS · GM 21253 · United States
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