HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Regulation of transcription of the human MRP7 gene. Characteristics of the basal promoter and identification of tumor-derived transcripts encoding additional 5' end heterogeneity.

Abstract
Studies focusing on the transcriptional regulation of MRP7 (multidrug resistance associated protein 7) gene expression in human tumor cells are described. As shown by real-time RT-PCR, expression of the MRP7 gene compared to the expression of the MRP1, 2 and 3 genes was less variable among the different cell types. MRP1, 2, 3 and 7 gene expression was highest in HepG2 cells compared to expression in CWR22Rv1 and TSU-PR1 cells. MRP7 gene expression was less than expression of the MRP1 and 2 genes in HepG2 cells but similar to MRP3 gene expression in this cell type and similar to or greater than expression of the MRP1, 2 and 3 genes in CWR22Rv1 and TSU-PR1 cells. Functional deletion analysis, in situ mutagenesis and electromobility shift assays (EMSA) showed that basal MRP7 promoter activity relied upon a proximal segment of the 5' flanking region 169 to 257 nt in length bearing an E2F site acting cooperatively with two closely positioned Sp1 sites. Two additional Sp1 sites further downstream were of secondary importance. The sequence of the E2F site was noncanonical and its interaction with E2F protein was confirmed by a competitive EMSA using a consensus E2F oligonucleotide probe and by demonstrating a supershift with the antibody against the E2F4 and E2F5 pocket protein, p107. 5' RACE carried out with CWR22Rv1 and HepG2 cells detected a single transcription start site (tsp) distal to the basal promoter and identified two new MRP7 transcripts with very short 5' UTR sequences compared to transcripts found by others in nontumorous human tissue. This 5' end heterogeneity infers a more complex intron-exon composition than hitherto shown.
AuthorsMagdalena Dabrowska, Francis M Sirotnak
JournalGene (Gene) Vol. 341 Pg. 129-39 (Oct 27 2004) ISSN: 0378-1119 [Print] Netherlands
PMID15474296 (Publication Type: Journal Article)
Chemical References
  • 5' Untranslated Regions
  • ABCC10 protein, human
  • Abcc10 protein, mouse
  • Multidrug Resistance-Associated Proteins
  • Nuclear Proteins
  • Oligonucleotide Probes
  • Protein Isoforms
  • RNA, Messenger
  • Recombinant Fusion Proteins
  • Transcription Factors
  • Luciferases
  • multidrug resistance-associated protein 1
Topics
  • 5' Flanking Region (genetics)
  • 5' Untranslated Regions (genetics)
  • Animals
  • Base Sequence
  • Binding Sites (genetics)
  • Cell Line, Tumor
  • Electrophoretic Mobility Shift Assay
  • Gene Expression Regulation
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Luciferases (genetics, metabolism)
  • Mice
  • Molecular Sequence Data
  • Multidrug Resistance-Associated Proteins (genetics)
  • Mutation
  • NIH 3T3 Cells
  • Nuclear Proteins (metabolism)
  • Oligonucleotide Probes (genetics, metabolism)
  • Promoter Regions, Genetic (genetics)
  • Protein Binding
  • Protein Isoforms (genetics)
  • RNA, Messenger (genetics, metabolism)
  • Recombinant Fusion Proteins (genetics, metabolism)
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Deletion
  • Transcription Factors (metabolism)
  • Transcription Initiation Site
  • Transcription, Genetic (genetics)
  • Transfection

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: