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PMID: 2832951 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Yeast HAP2 and HAP3: transcriptional activators in a heteromeric complex.

Science (New York, N.Y.) ·Vol. 240 ·No. 4850 ·1988-04-15 ·Pages 317-21

Hahn S, Guarente L

Abstract

Transcription of the yeast C upsilon C1 gene (iso-1-cytochrome c) is regulated in part by the upstream activation site UAS2. Activity of UAS2 requires both the HAP2 and HAP3 activators, which bind to UAS2 in an interdependent manner. To distinguish whether these factors bound to UAS2 cooperatively or formed a complex in the absence of DNA, HAP2 and HAP3 were tagged by gene fusion to LexA and beta-galactosidase, respectively, and purified through four chromatographic steps. The copurification of LexA-HAP2, HAP3 beta-galactosidase, and UAS2 binding activity shows that HAP2 and HAP3 associate in the absence of DNA to form a multisubunit activation complex.

MeSH Terms
Bacterial Proteins/genetics Cloning, Molecular Cytochrome c Group/genetics Cytochromes c Galactosidases/genetics Genes Genes, Fungal Genes, Regulator Saccharomyces cerevisiae Proteins Serine Endopeptidases Transcription, Genetic beta-Galactosidase/genetics
Chemicals
Bacterial Proteins CYC1 protein, S cerevisiae Cytochrome c Group LexA protein, Bacteria Saccharomyces cerevisiae Proteins Cytochromes c Galactosidases beta-Galactosidase Serine Endopeptidases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Hahn S
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
Guarente L
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1988-04-15
Pages
317-21
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIGMS NIH HHS · 5RO1 GM3044-05 · United States
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