Isolation, tissue distribution, and chromosomal localization of a novel testis-specific human four-transmembrane gene related to CD20 and Fc epsilon RI-beta
Md. Hulett et al., Isolation, tissue distribution, and chromosomal localization of a novel testis-specific human four-transmembrane gene related to CD20 and Fc epsilon RI-beta, BIOC BIOP R, 280(1), 2001, pp. 374-379
Citations number
12
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
CD20 and the beta subunit of the high affinity receptor for IgE (Fc epsilon
RI beta) are related four-transmembrane molecules that are expressed on th
e surface of hematopoietic cells and play crucial roles in signal transduct
ion. Herein, we report the identification and characterization of a human g
ene, TETM4 that encodes a novel four-transmembrane protein related to CD20
and Fc epsilon RI beta. The predicted TETM4 protein is 200 amino acids and
contains four putative transmembrane regions, N- and C-terminal cytoplasmic
domains, and three inter-transmembrane loop regions. TETM4 shows 31.0 and
23.2% overall identity with CD20 and Fc epsilon RI beta respectively, with
the highest identity in the transmembrane regions, whereas the N- and C-ter
mini and inter-transmembrane loops are more divergent. Northern blot and RT
-PCR analysis suggest that TETM4 mRNA has a highly restricted tissue distri
bution, being expressed selectively in the testis, Using fluorescence in si
tu hybridization and radiation hybrid analysis, the TETM4 gene has been loc
alized to chromosome 11q12. The genes for CD20 and Fc epsilon RI beta have
also been mapped to the same region of chromosome 11 (11q12-13.1), suggesti
ng that these genes have evolved by duplication to form a family of four-tr
ansmembrane genes. TETM4 is the first nonhematopoietic member of the CD20/F
c epsilon RI beta family, and like its hematopoietic-specific relatives, it
may be involved in signal transduction as a component of a multimeric rece
ptor complex. (C) 2001 Academic Press.