IDENTIFICATION OF POTENTIAL REGULATORY ELEMENTS IN THE FAR-UPSTREAM REGION OF THE ARABIDOPSIS-THALIANA PLASTOCYANIN PROMOTER

Citation
U. Fisscher et al., IDENTIFICATION OF POTENTIAL REGULATORY ELEMENTS IN THE FAR-UPSTREAM REGION OF THE ARABIDOPSIS-THALIANA PLASTOCYANIN PROMOTER, Plant molecular biology, 26(3), 1994, pp. 873-886
Citations number
47
Categorie Soggetti
Plant Sciences",Biology
Journal title
ISSN journal
01674412
Volume
26
Issue
3
Year of publication
1994
Pages
873 - 886
Database
ISI
SICI code
0167-4412(1994)26:3<873:IOPREI>2.0.ZU;2-O
Abstract
The far-upstream region of the Arabidopsis thaliana plastocyanin (Pc) promoter acts positively on transcription. This -1580 to -710 region ( relative to the translation start site) has enhancer-like properties s ince it is also functional when situated downstream of the gene. Using tobacco nuclear extracts, this region was tested for protein-binding sites. Two short binding sequences were identified. The AT-rich sequen ce separating these binding sites shows extensive homology to the sequ ences separating the paired GT-1-binding sites of the pea rbcS-3A prom oter. The requirements for complex formation strongly suggest that a G T-1-like protein binds to the two identified boxes in the Pc promoter. Sequence comparisons revealed that both boxes fit within the moderate consensus sequence needed for GT-1 binding. This GT-1-like DNA-bindin g activity is present in light-grown as well as in dark-adapted plants . Therefore, the possible role for GT-1 in light regulation of transcr iption does not depend upon its de novo synthesis. In some of the gel mobility shift assays, an additional DNA-protein complex was formed. T he formation of this complex was only observed if the heteropolymer po ly(dAdT).poly(dAdT) was used as a non-specific competitor and was depe ndent on the CpG density of the probe used.