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PMID: 6341997 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Identification of AAS genes and their regulatory role in general control of amino acid biosynthesis in yeast.

Penn MD, Galgoci B, Greer H

Abstract

In yeast, most amino acid biosynthetic pathways are coregulated: starvation for a single amino acid results in derepression of enzyme activities for many different biosynthetic pathways. This phenomenon is referred to as "general control of amino acid biosynthesis." In this paper we describe the isolation and characterization of 43 amino acid analog-sensitive (aas-) mutants that are perturbed in this general regulatory system. These 43 mutations define four unlinked complementation groups, AAS101, AAS102, AAS103, and AAS104, two of which identify previously unreported genes involved in general control. These aas mutants are unable to derepress a number of amino acid biosynthetic genes, resulting in increased sensitivity to amino acid analogs, reduced growth rates, and reduced enzyme activity levels under amino acid starvation conditions. Thus, the AAS+ gene products function as positive regulatory elements for this system. We show that the AAS genes mediate these effects by regulating the mRNA levels of genes under their control.

MeSH Terms
Alcohol Oxidoreductases/metabolism Amino Acids/biosynthesis Amitrole/pharmacology Canavanine/pharmacology Ethionine/pharmacology Genes, Regulator Genetic Linkage Mutation RNA, Messenger/metabolism Saccharomyces cerevisiae/drug effects,genetics Tryptophan/analogs & derivatives,pharmacology
Chemicals
Amino Acids RNA, Messenger 5-methyltryptophan Canavanine Tryptophan Alcohol Oxidoreductases histidinol dehydrogenase Ethionine Amitrole
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Penn M D
Galgoci B
Greer H
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27 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1983-05-00
Pages
2704-8
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC393896
Subset
IM
Grants
NIGMS NIH HHS · GM25207 · United States
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