Cloning and transcriptional analysis of the promoter of the human type 2 desmocollin gene (DSC2)

被引:25
作者
Marsden, MD
Collins, JE
Greenwood, MD
Adams, MJ
Fleming, TP
Magee, AI
Buxton, RS
机构
[1] NATL INST MED RES, DIV MEMBRANE BIOL, LONDON NW7 1AA, ENGLAND
[2] UNIV SOUTHAMPTON, SCH BIOL SCI, DEPT BIOL, SOUTHAMPTON SO16 7PX, HANTS, ENGLAND
基金
英国医学研究理事会;
关键词
cell junction; desmosome; cadherin; genomic clone; reporter gene; mouse embryo;
D O I
10.1016/S0378-1119(96)00715-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The desmocollins, together with the desmogleins, are members of the cadherin family and constitute the adhesive proteins of the desmosome type 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 isoform expressed in the developing mouse embryo and that has the most widespread tissue distribution in epithelia and also in desmosome-bearing non-epithelial tissues. Analysis of the 5' upstream region by DNA sequencing and Southern blotting suggested that it contained a CpG island, and a major site of transcription initiation 201 bp upstream of the translation start site was found by RNase protection and primer extension. There were no obvious CCAAT or TATA boxes present. Analysis of 1.9 kb upstream of the translation start site revealed consensus binding sites for transcription factors including Ap-2 and Sp-1, and motifs common to the promoters of other epithelially expressed genes such as keratin 14 and the desmoglein genes DSG1 and DSG3. Deletion derivatives defined a promoter of 525 bp which was active in epithelial cells and in mouse blastocysts with an intact epithelium. This promoter showed reduced expression in non-epithelial cells.
引用
收藏
页码:237 / 247
页数:11
相关论文
共 42 条
[1]   EXTRACELLULAR DOMAIN OF PEMPHIGUS-VULGARIS ANTIGEN (DESMOGLEIN-3) MEDIATES WEAK HEMOPHILIC ADHESION [J].
AMAGAI, M ;
KARPATI, S ;
KLAUSKOVTUN, V ;
UDEY, MC ;
STANLEY, JR .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1994, 102 (04) :402-408
[2]   CHARACTERIZATION OF HUMAN CARDIAC DESMOSOMAL CADHERINS [J].
ANGST, BD ;
BUXTON, RS ;
MAGEE, AI .
CARDIAC GROWTH AND REGENERATION, 1995, 752 :101-104
[3]  
ARNEMANN J, 1993, J CELL SCI, V104, P741
[4]  
AUFFRAY C, 1980, EUR J BIOCHEM, V107, P303
[5]   THE E-CADHERIN PROMOTER - FUNCTIONAL-ANALYSIS OF A G.C-RICH REGION AND AN EPITHELIAL CELL-SPECIFIC PALINDROMIC REGULATORY ELEMENT [J].
BEHRENS, J ;
LOWRICK, O ;
KLEINHITPASS, L ;
BIRCHMEIER, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (24) :11495-11499
[6]   CPG-RICH ISLANDS AND THE FUNCTION OF DNA METHYLATION [J].
BIRD, AP .
NATURE, 1986, 321 (6067) :209-213
[7]   DIFFERENTIALLY EXPRESSED BOVINE CYTOKERATIN GENES - ANALYSIS OF GENE LINKAGE AND EVOLUTIONARY CONSERVATION OF 5'-UPSTREAM SEQUENCES [J].
BLESSING, M ;
ZENTGRAF, H ;
JORCANO, JL .
EMBO JOURNAL, 1987, 6 (03) :567-575
[8]  
Blumenberg Miroslav, 1993, P1
[9]   TRANSCRIPTIONAL REGULATION OF THE HUMAN E-CADHERIN GENE IN HUMAN PROSTATE-CANCER CELL-LINES - CHARACTERIZATION OF THE HUMAN E-CADHERIN GENE PROMOTER [J].
BUSSEMAKERS, MJG ;
GIROLDI, LA ;
VANBOKHOVEN, A ;
SCHALKEN, JA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 203 (02) :1284-1290
[10]  
Buxton R S, 1992, Semin Cell Biol, V3, P157