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PMID: 2780550 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

A CACGTG motif of the Antirrhinum majus chalcone synthase promoter is recognized by an evolutionarily conserved nuclear protein.

Staiger D, Kaulen H, Schell J

Abstract

In the chalcone synthase gene of Antirrhinum majus (snapdragon), 150 base pairs of the 5' flanking region contain cis-acting signals for UV light-induced expression. A nuclear factor, designated CG-1, specifically recognizes a hexameric motif with internal dyad symmetry, CACGTG, located within this light-responsive sequence. Binding of CG-1 is influenced by C-methylation of the CpG dinucleotide in the recognition sequence. CG-1 is a factor found in a variety of dicotyledonous plant species including Nicotiana tabacum, A. majus, Petunia hybrida, Arabidopsis thaliana, and Glycine max. CACGTG motifs contained within trans-acting factor recognition sites in various other plant promoters can interact with CG-1. In addition, the binding site of the human adenovirus major late transcription factor USF can compete for CG-1 binding to the chalcone synthase promoter. This suggests an evolutionary conservation of trans-acting factor recognition sites involved in divergent mechanisms of gene control.

MeSH Terms
Acyltransferases/genetics Base Sequence Biological Evolution Genes Molecular Sequence Data Nuclear Proteins/genetics,metabolism Oligonucleotide Probes Plants/enzymology,genetics Plants, Toxic Promoter Regions, Genetic Protein Binding Tobacco/metabolism
Chemicals
Nuclear Proteins Oligonucleotide Probes Acyltransferases flavanone synthetase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Staiger D
Max-Planck-Institut für Züchtungsforschung, Cologne, Federal Republic of Germany.
Kaulen H
Schell J
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24 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
1989-09-00
Pages
6930-4
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC297964
Subset
IM
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