Identification and characterization of a novel promoter of the mouse mu opioid receptor gene (Oprm) that generates eight splice variants Journal Article


Author: Pan, Y. X.
Article Title: Identification and characterization of a novel promoter of the mouse mu opioid receptor gene (Oprm) that generates eight splice variants
Abstract: Our previous studies isolated and characterized eight splicing variants containing exon 11 as the first coding exon. The location of exon 11 about 10 kb upstream from exon 1 dual promoters implied another promoter to drive expression of the exon 11 variants. I now identify the second promoter in the 5′-flanking region of exon 11. One major transcriptional start point was determined. Sequence analysis indicated that the 5′-flanking region of the exon 11 contained a putative TATA box, several CAAT boxes and a number of cis-acting elements. Functional analysis suggested that exon 11 promoter activity was most evident in neuronal-like cells. A basal core region containing the TATA box, a negative region and a positive region were identified. Electrophoretic mobility shift assays with the nuclear extracts from NIE-115 cells revealed several protein complexes that likely contained TATA box-associated factors, NF-1-like and cMyc-Max-like proteins, respectively. It also showed that a TATA-binding protein specifically bound to the TATA box fragment. Mutation analysis suggested that the TATA box in the basal core region played a fundamental role in the exon 11 promoter, whereas the NF-1 site acted as a positive element. © 2002 Elsevier Science B.V. All rights reserved.
Keywords: controlled study; human cell; promoter region; sequence analysis; exon; mutation; exons; sequence deletion; nonhuman; animal cell; mouse; animals; mice; animal tissue; protein; protein binding; tumor cells, cultured; mutational analysis; nuclear proteins; dna; transcription regulation; molecular sequence data; gene identification; alternative splicing; base sequence; plasmids; dna flanking region; dna sequence; binding sites; gel mobility shift assay; electrophoretic mobility shift assay; protein variant; mu opiate receptor; receptors, opioid, mu; cis acting element; gene activity; transcription initiation site; sequence analysis, dna; cho cells; cricetinae; cell extract; tata box; nuclear factor; promoter regions (genetics); 5' flanking region; tata binding protein; tata-box binding protein; humans; human; priority journal; article; cmyc-max; nf-1
Journal Title: Gene
Volume: 295
Issue: 1
ISSN: 0378-1119
Publisher: Elsevier Science, Inc.  
Date Published: 2002-07-24
Start Page: 97
End Page: 108
Language: English
DOI: 10.1016/s0378-1119(02)00825-9
PUBMED: 12242016
PROVIDER: scopus
DOI/URL:
Notes: Export Date: 14 November 2014 -- Source: Scopus
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  1. Yingxian Pan
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