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Transcriptional regulation of the major zinc uptake protein hZip1 in prostate cancer cells.
- Source :
-
Gene [Gene] 2009 Feb 15; Vol. 431 (1-2), pp. 39-46. Date of Electronic Publication: 2008 Nov 05. - Publication Year :
- 2009
-
Abstract
- hZip1 has been characterized as the major zinc uptake transporter regulating the accumulation of zinc in prostate cells. The mechanisms regulating expression of hZip1 have not been described. To explore the mechanisms of transcriptional regulation of the hZip1 gene, we determined the putative promoter sequence for hZip1 and identified the potential transcription start site within the predicted hZip1 promoter region. To further characterize the promoter region for basal hZip1 transcription, 3' and 5' deletion constructs and constructs with mutated binding sites for putative transcription factors were generated by PCR amplification and assessed for transcriptional activity with a luciferase reporter assay in PC-3 prostate cancer cells. The ability of the specific transcription factors to bind the hZip1 core promoter was confirmed by EMSA, GelSupershift and ChIP assays. Our experiments identified the core promoter region responsible for constitutive expression of hZip1 and demonstrated critical roles for SP1 and CREB1 in transcriptional regulation of the hZip1 gene in prostate cancer cells.
- Subjects :
- Animals
Base Sequence
Cell Line, Tumor
Computational Biology
Cyclic AMP Response Element-Binding Protein metabolism
Humans
Male
Mice
Molecular Sequence Data
Promoter Regions, Genetic genetics
Protein Binding
RNA, Small Interfering metabolism
Sequence Alignment
Sp1 Transcription Factor metabolism
Transcription Initiation Site
Transfection
Cation Transport Proteins genetics
Gene Expression Regulation, Neoplastic
Prostatic Neoplasms genetics
Transcription, Genetic
Zinc metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0038
- Volume :
- 431
- Issue :
- 1-2
- Database :
- MEDLINE
- Journal :
- Gene
- Publication Type :
- Academic Journal
- Accession number :
- 19026724
- Full Text :
- https://doi.org/10.1016/j.gene.2008.10.015