CLONING AND TRANSCRIPTIONAL ANALYSIS OF THE PROMOTER OF THE HUMAN TYPE-2 DESMOCOLLIN GENE (DSC2)

Citation
Md. Marsden et al., CLONING AND TRANSCRIPTIONAL ANALYSIS OF THE PROMOTER OF THE HUMAN TYPE-2 DESMOCOLLIN GENE (DSC2), Gene, 186(2), 1997, pp. 237-247
Citations number
42
Categorie Soggetti
Genetics & Heredity
Journal title
GeneACNP
ISSN journal
03781119
Volume
186
Issue
2
Year of publication
1997
Pages
237 - 247
Database
ISI
SICI code
0378-1119(1997)186:2<237:CATAOT>2.0.ZU;2-R
Abstract
The desmocollins, together with the desmogleins, are members of the ca dherin family and constitute the adhesive proteins of the desmosome ty pe of cell-cell junction. Here we describe a study of the promoter of the human form of the DSC2 gene which is the equivalent of the first i soform expressed in the developing mouse embryo and that has the most widespread tissue distribution in epithelia and also in desmosome-bear ing non-epithelial tissues. Analysis of the 5' upstream region by DNA sequencing and Southern blotting suggested that it contained a CpG isl and, and a major site of transcription initiation 201 bp upstream of t he translation start site was found by RNase protection and primer ext ension. There were no obvious CCAAT or TATA boxes present. Analysis of 1.9 kb upstream of the translation start site revealed consensus bind ing sites for transcription factors including Ap-2 and Sp-1, and motif s common to the promoters of other epithelially expressed genes such a s keratin 14 and the desmoglein genes DSG1 and DSG3. Deletion derivati ves defined a promoter of 525 bp which was active in epithelial cells and in mouse blastocysts with an intact epithelium. This promoter show ed reduced expression in non-epithelial cells.