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PMID: 8246964 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Properties of initiator-associated transcription mediated by GAL4-VP16.

Molecular and cellular biology ·Vol. 13 ·No. 12 ·1993-12-00 ·Pages 7469-75

Chang C, Gralla JD

Abstract

Transcription associated with a terminal deoxynucleotide transferase gene initiator element is shown to respond to the transcription factor GAL4-VP16 both in vivo and in vitro. High-level transcription requires both an intact initiator element and bound activator. Transcription from this initiator-directed promoter is synergistic in vivo in that five GAL4 DNA binding sites yield 36 times the expression of a single site. Promoters dominated by initiator and TATA elements respond similarly to several GAL4-based activators, including GAL4-Sp1, GAL4-CTF, GAL4(1-147), GAL4-p53, GAL4-C/EBP, and GAL4-ER(EF), as well as GAL4-VP16 and Sp1. These and other similarities suggest that primary activation of TATA- and initiator-dominated promoters occurs at common steps. Since the initial assembly steps do not appear to be common for the two promoter types, the results place interesting constraints on models for how activation occurs.

Related Genes
TdT
MeSH Terms
Animals Base Sequence Cell Line DNA Nucleotidylexotransferase/genetics DNA, Fungal/genetics Fungal Proteins/genetics Gene Expression Regulation, Fungal Genes, Fungal Molecular Sequence Data Promoter Regions, Genetic Saccharomyces cerevisiae/genetics Trans-Activators/genetics Transcription, Genetic
Chemicals
DNA, Fungal Fungal Proteins Gal-VP16 Trans-Activators DNA Nucleotidylexotransferase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Chang C
Department of Chemistry and Biochemistry, University of California, Los Angeles 90024-1569.
Gralla J D
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40 references, click to expand
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Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1993-12-00
Pages
7469-75
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC364818
Subset
IM
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