cDNA cloning, chromosomal mapping, and expression analysis of human VE-Cadherin-2

被引:11
|
作者
Ludwig, D
Lorenz, J
Dejana, E
Bohlen, P
Hicklin, DJ
Witte, L
Pytowski, B
机构
[1] ImClone Syst Inc, New York, NY 10014 USA
[2] Mario Negri Inst Pharmacol Res, Dept Human Immunol & Cell Biol, Milan, Italy
关键词
D O I
10.1007/s003350010186
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Murine vascular endothelial cadherin-2 (VE-cad-2) is a cellular adhesion molecule that is distinct from vascular endothelial cadherin 1 (VE-cad-1) in that it does not interact with catenins and does not appear to affect cell migration or growth. In this study, we have cloned a full-length cDNA of the human homolog of VE-cad-2 and used it to map the chromosomal locus of the VE-cad-2 gene. Human VE-cad-2 maps to Chromosome (Chr) 5q31. The cDNA of human VE-cad-2 is highly homologous to mouse VE-cad-2, except for a C-terminal tail. The genomic structure of VE-cad-2 is strikingly similar to that reported for a large family of neuronal protocadherin genes mapped to Chr 5q, yet the amino acid sequences between VE-cad-2 and the protocadherins are substantially divergent. The promoter of human VE-cad-2 contains two TATA boxes and transcription initiates from a single site 3' to these elements. Similar to mouse VE-cad-2, the human gene is expressed primarily in highly vascularized tissues.
引用
收藏
页码:1030 / 1033
页数:4
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