Definition of an Fc receptor-related gene (FcRX) expressed in human and mouse B cells

被引:34
作者
Davis, RS
Li, HT
Chen, CC
Wang, YH
Cooper, MD
Burrows, PD
机构
[1] Univ Alabama, Div Hematol Oncol, Birmingham, AL 35294 USA
[2] Univ Alabama, Div Dev & Clin Immunol, Birmingham, AL 35294 USA
[3] Univ Alabama, Dept Med, Birmingham, AL 35294 USA
[4] Univ Alabama, Dept Pediat, Birmingham, AL 35294 USA
[5] Univ Alabama, Dept Pathol, Birmingham, AL 35294 USA
[6] Univ Alabama, Dept Microbiol, Birmingham, AL 35294 USA
[7] Univ Alabama, Howard Hughes Med Inst, Birmingham, AL 35294 USA
关键词
B cell-specific gene; chromosome; 1; Fc receptor;
D O I
10.1093/intimm/dxf074
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The recent identification of five human Fc receptor (FcR) homologs, hFcRH1-5, has extended the known FcR family and identified an unanticipated richness of the chromosome 1q region in genes encoding potential Ig-binding proteins. In a database search for additional relatives of this family we identified expressed sequence tag representatives of a new FcR-related molecule (hFcRX) and its mouse ortholog (mFcRX). The FcRX cDNAs were cloned from human lymph node and mouse spleen cDNA libraries. hFcRX is located centromeric of FcgammaRII and FcgammaRIII at 1q23, and its mouse ortholog resides in a syntenic region of chromosome 1. The genes encode proteins with 67% interspecies identity that lack both N-linked glycosylation sites and transmembrane regions. Two of the four FcRX domains are Ig-like, and share characteristics similar to FcgammaRI domains 2 and 3, having 28% overall extracellular identity with hFcgammaRI and 27% identity with mFcgammaRI respectively. FcRX transcripts are found primarily in secondary lymphoid tissues, where they are expressed by B lineage cells. FcRX thus may function as a secreted or intracellular protein in normal and neoplastic B cells.
引用
收藏
页码:1075 / 1083
页数:9
相关论文
共 56 条
  • [1] Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling
    Alizadeh, AA
    Eisen, MB
    Davis, RE
    Ma, C
    Lossos, IS
    Rosenwald, A
    Boldrick, JG
    Sabet, H
    Tran, T
    Yu, X
    Powell, JI
    Yang, LM
    Marti, GE
    Moore, T
    Hudson, J
    Lu, LS
    Lewis, DB
    Tibshirani, R
    Sherlock, G
    Chan, WC
    Greiner, TC
    Weisenburger, DD
    Armitage, JO
    Warnke, R
    Levy, R
    Wilson, W
    Grever, MR
    Byrd, JC
    Botstein, D
    Brown, PO
    Staudt, LM
    [J]. NATURE, 2000, 403 (6769) : 503 - 511
  • [2] ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
  • [3] Divergent and convergent evolution of NK-cell receptors
    Barten, R
    Torkar, M
    Haude, A
    Trowsdale, J
    Wilson, MJ
    [J]. TRENDS IN IMMUNOLOGY, 2001, 22 (01) : 52 - 57
  • [4] Spontaneous autoimmune disease in FcγRIIB-deficient mice results from strain-specific epistasis
    Bolland, S
    Ravetch, JV
    [J]. IMMUNITY, 2000, 13 (02) : 277 - 285
  • [5] Borges L, 1997, J IMMUNOL, V159, P5192
  • [6] Brossay L, 1998, J IMMUNOL, V160, P3681
  • [7] Burdin N, 1998, J IMMUNOL, V161, P3271
  • [8] The IgG Fc receptor, FcγRIIB, is a target for deregulation by chromosomal translocation in malignant lymphoma
    Callanan, MB
    Le Baccon, P
    Mossuz, P
    Duley, S
    Bastard, C
    Hamoudi, R
    Dyer, MJ
    Klobeck, G
    Rimokh, R
    Sotto, JJ
    Leroux, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (01) : 309 - 314
  • [9] Fc receptor biology
    Daeron, M
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 : 203 - 234
  • [10] Davis RS, 2002, CURR TOP MICROBIOL, V266, P85