Home LiteratureArticle Details
PMID: 3128739 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

The JUN oncoprotein, a vertebrate transcription factor, activates transcription in yeast.

Nature ·Vol. 332 ·No. 6165 ·1988-04-14 ·Pages 649-50

Struhl K

Abstract

Transcriptional activation of RNA polymerase II in eukaryotic organisms ranging from yeasts to mammals has many common features such as enhancer elements, TATA elements, and activator proteins that bind specifically to promoter DNA. The JUN oncoprotein, which causes sarcomas in chickens, shows significant homology to the DNA-binding domain of GCN4, a yeast protein that stimulates transcription of the amino acid biosynthetic genes. The GCN4 and JUN proteins bind the same DNA sequences, consensus ATGA(C/G)TCAT, even though the DNA-binding domains are only 45% identical in amino acid sequence. The JUN protein almost certainly represents the oncogenic version of the normal AP-1 transcription factor, suggesting an evolutionary relationship between yeast and vertebrate activator proteins. Here, I demonstrate that JUN efficiently activates transcription in yeast either through its own or a heterologous DNA-binding domain. As is the case for yeast activator proteins, transcriptional stimulation by JUN requires an acidic activation region distinct from the DNA-binding domain. The functional interchangeability between yeast and vertebrate transcription factors strongly suggests a basic similarity in the molecular mechanism of eukaryotic transcriptional activation.

MeSH Terms
Amino Acid Sequence Bacterial Proteins/genetics,metabolism Binding Sites DNA/metabolism DNA, Recombinant DNA-Binding Proteins Escherichia coli/genetics Fungal Proteins/genetics,metabolism Molecular Sequence Data Oncogene Protein p65(gag-jun) Plasmids Protein Kinases Recombinant Fusion Proteins Repressor Proteins Retroviridae Proteins/metabolism,pharmacology Saccharomyces cerevisiae/genetics Saccharomyces cerevisiae Proteins Serine Endopeptidases Transcription Factors/genetics,metabolism,pharmacology Transcription, Genetic/drug effects beta-Galactosidase/genetics,metabolism
Chemicals
Bacterial Proteins DNA, Recombinant DNA-Binding Proteins Fungal Proteins LexA protein, Bacteria Oncogene Protein p65(gag-jun) Recombinant Fusion Proteins Repressor Proteins Retroviridae Proteins Saccharomyces cerevisiae Proteins Transcription Factors DNA Protein Kinases beta-Galactosidase Serine Endopeptidases
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Struhl K
Department of Biological Chemistry, Harvard Medical School, Boston, Massachusetts 02115.
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1988-04-14
Pages
649-50
Language
English
Region
England
NLM ID
0410462
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com