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Transcriptional Activation of the Human Rod cGMP-Phosphodiesterase -Subunit Gene Is Mediated by an Upstream AP-1 Element
Author(s) -
Adriana Di Polo,
L.E. Lerner,
Debora B. Farber
Publication year - 1997
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/25.19.3863
Subject(s) - biology , microbiology and biotechnology , phosphodiesterase , gene , reporter gene , transcription (linguistics) , gene expression , protein subunit , regulation of gene expression , promoter , transcriptional regulation , signal transduction , genetics , biochemistry , enzyme , linguistics , philosophy
During photoactivation retinal cGMP-phosphodiesterase (PDE) mediates signal transduction in the photoreceptor outer segments. Mutations in the beta-subunit gene of rod-specific PDE (beta-PDE) have been associated with inherited retinal degeneration in a number of species, including human. Here we have investigated the proximal upstream sequences that participate in transcriptional activation of this gene. Transient transfections demonstrated that the sequence from -72 to +53 bp contained sufficient information to direct high levels of gene expression in cells of retinal origin. Deletion or mutagenesis of an AP-1 motif present in this region caused 90-95% reduction in reporter gene expression. By gel mobility shift assay we demonstrated specific interactions between putative nuclear transcription factors and this AP-1 element. These findings indicate that the proximal AP-1 site in the human beta-PDE promoter is functionally relevant and necessary for transcriptional activation of this gene.

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