MOUSE HOMOLOG OF C33-ANTIGEN (CD82), A MEMBER OF THE TRANSMEMBRANE-4 SUPERFAMILY - COMPLEMENTARY-DNA, GENOMIC STRUCTURE, AND EXPRESSION

Citation
M. Nagira et al., MOUSE HOMOLOG OF C33-ANTIGEN (CD82), A MEMBER OF THE TRANSMEMBRANE-4 SUPERFAMILY - COMPLEMENTARY-DNA, GENOMIC STRUCTURE, AND EXPRESSION, Cellular immunology, 157(1), 1994, pp. 144-157
Citations number
41
Categorie Soggetti
Cytology & Histology",Immunology
Journal title
ISSN journal
00088749
Volume
157
Issue
1
Year of publication
1994
Pages
144 - 157
Database
ISI
SICI code
0008-8749(1994)157:1<144:MHOC(A>2.0.ZU;2-C
Abstract
C33 Ag (CD82) is a member of the transmembrane 4 superfamily (TM4SF) a nd an activation Ag of T-cells. Recent studies have shown that CD82 as sociates with CD4 or CD8 and delivers costimulatory signals for the TC R/CD3 pathway. We have isolated cDNA and genomic clones of mouse CD82. Mouse CD82 has 266 amino acid residues with 76% identity to human CD8 2. The mouse CD82 gene consists of nine exons and spans more than 20 k b of genomic DNA. The genomic organization of CD82 is quite similar to that of three other TM4SF members whose genomic structures were descr ibed, i.e., Tapa-1 (CD81), CD53, and CD63. By mapping the 5' end of CD 82 transcripts, we found a single major transcription initiation site 144 bp upstream of the ATG initiation codon. We also determined the se quence of the 5' flanking region of CD82 gene for about 2 kb. The 5' n anking sequence has a housekeeping promoter with potential binding mot ifs for various transcriptional factors. Northern blot analysis showed quite variable expression of the CD82 gene among different organs. Th e highest expression was seen in the spleen and the kidney. The expres sion was low in skeletal muscle and hardly detectable in the heart. No rthern blot analysis was also carried out for CD81, CD53, and CD63. Th e expression of the CD81 gene was ubiquitous and similar among differe nt organs, while that of CD53 was seen only in the spleen. The express ion of the CD63 gene was ubiquitous, with the highest expression in th e kidney. These results together with the comparison of the structures of 5' flanking sequences of these genes indicate distinct regulations of gene expression for these four members of TM4SF. (C) 1994 Academic Press, Inc.