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PMID: 3031464 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Ty1 sequence with enhancer and mating-type-dependent regulatory activities.

Molecular and cellular biology ·Vol. 7 ·No. 1 ·1987-01-00 ·Pages 258-65

Errede B, Company M, Hutchison CA

Abstract

Some insertion mutations in Saccharomyces cerevisiae activate the expression of adjacent structural genes. The CYC7-H2 mutation is a Ty1 insertion 5' to the iso-2-cytochrome c coding region of CYC7. The Ty1 insertion causes a 20-fold increase in CYC7 expression in a and alpha haploid cell types of S. cerevisiae. This activation is repressed in the a/alpha diploid cell type. Previous computer analysis of the CYC7-H2 Ty1 activator region identified two related sequences with homology both to mammalian enhancers and to a yeast a/alpha control site. A 112-base-pair (bp) DNA fragment encompassing one of these blocks of homology functioned as one component of the Ty1 activator. A 28-bp synthetic oligonucleotide with the wild-type homology block sequence was also functional. A single base pair mutation within the enhancer core of the synthetic 28-bp regulatory element reduced its activation ability to near background amounts. In addition, the 112-bp Ty1 fragment by itself functioned as a target for repression of adjacent gene expression in a/alpha diploid cells.

MeSH Terms
Amino Acid Sequence Base Sequence Cytochrome c Group/genetics Cytochromes c DNA Transposable Elements Diploidy Enhancer Elements, Genetic Genes Genes, Fungal Genes, Mating Type, Fungal Genes, Regulator Mutation Nucleic Acid Hybridization Plasmids Saccharomyces cerevisiae/genetics Transcription, Genetic
Chemicals
Cytochrome c Group DNA Transposable Elements iso-2-cytochrome C Cytochromes c
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Errede B
Company M
Hutchison C A
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1987-01-00
Pages
258-65
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC365065
Subset
IM
Grants
NIAID NIH HHS · AI-08998 · United States
NIGMS NIH HHS · GM-30619 · United States
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