A cluster of ten novel MHC class I related genes on human chromosome 6q24.2-q25.3

被引:122
作者
Radosavljevic, M
Cuillerier, B
Wilson, MJ
Clément, O
Wicker, S
Gilfillan, S
Beck, S
Trowsdale, J
Bahram, S
机构
[1] INSERM, Ctr Rech Immunol Hematol, CReS, F-67085 Strasbourg, France
[2] Dept Pathol, Div Immunol, Cambridge CB2 1QP, England
[3] Basel Inst Immunol, CH-4005 Basel, Switzerland
[4] Sanger Ctr, Cambridge CB10 1SA, England
基金
英国惠康基金;
关键词
major histocompatibility complex; MHC; MIC; RAET1; chromosome; 6q; t-complex;
D O I
10.1006/geno.2001.6673
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have identified a novel family of human major histocompatibility complex (MHC) class I genes. This MHC class I related gene family is defined by 10 members, among which 6 encode potentially functional glycoproteins. The 180-kb cluster containing them has been generated by serial duplication and minimal diversification of an ancestral prototype. They are not located within the MHC on 6p21.3, but near the tip of its long arm at q24.2-q25.3, close to the human equivalent of the mouse H2-linked t-complex, a subchromosomal region syntenic to a segment of mouse chromosome 10 harboring the orthologous MHC class I related retinoic acid early transcript loci, Raet1a-d. Hence we have named the identified loci RAET1E-N. Human RAET1 products are all devoid of the membrane-proximal immunoglobulin-like 0 domain and most, but not all, are predicted to remain membrane-anchored via glycosylphosphatidylinositol linkage and are shown to display an atypical pattern of polymorphism. RAET1 transcripts are absent from hematopoietic tissues, but largely expressed in tumors. The involvement of orthologous mouse RAET1A-D/H60 in natural killer and T-cell activation through NKG2D engagement augurs a similar function for the human RAET1 proteins.
引用
收藏
页码:114 / 123
页数:10
相关论文
共 39 条
[1]   COMPLETE AMINO-ACID SEQUENCE OF HUMAN-PLASMA ZN-ALPHA-2-GLYCOPROTEIN AND ITS HOMOLOGY TO HISTOCOMPATIBILITY ANTIGENS [J].
ARAKI, T ;
GEJYO, F ;
TAKAGAKI, K ;
HAUPT, H ;
SCHWICK, HG ;
BURGI, W ;
MARTI, T ;
SCHALLER, J ;
RICKLI, E ;
BROSSMER, R ;
ATKINSON, PH ;
PUTNAM, FW ;
SCHMID, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (03) :679-683
[2]   A 2ND LINEAGE OF MAMMALIAN MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I GENES [J].
BAHRAM, S ;
BRESNAHAN, M ;
GERAGHTY, DE ;
SPIES, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6259-6263
[3]  
Bahram S, 2000, Adv Immunol, V76, P1
[4]   Activation of NK Cells and T Cells by NKG2D, a Receptor for Stress-Inducible MICA [J].
Bauer, Stefan ;
Groh, Veronika ;
Wu, Jun ;
Steinle, Alexander ;
Phillips, Joseph H. ;
Lanier, Lewis L. ;
Spies, Thomas .
JOURNAL OF IMMUNOLOGY, 2018, 200 (07) :2231-2233
[5]   Isochores and the evolutionary genomics of vertebrates [J].
Bernardi, G .
GENE, 2000, 241 (01) :3-17
[6]   HUMAN HOMOLOGS OF 2 TESTES-EXPRESSED LOCI ON MOUSE CHROMOSOME-17 MAP TO OPPOSITE ARMS OF CHROMOSOME-6 [J].
BIBBINS, KB ;
TSAI, JY ;
SCHIMENTI, J ;
SARVETNICK, N ;
ZOGHBI, HY ;
GOODFELLOW, P ;
SILVER, LM .
GENOMICS, 1989, 5 (01) :139-143
[7]   GENETIC-MAPPING OF 3 HUMAN HOMOLOGS OF MURINE T-COMPLEX GENES LOCALIZES TCP10 TO 6Q27, 15 CM DISTAL TO TCP1 AND PLG [J].
BLANCHE, H ;
WRIGHT, LG ;
VERGNAUD, G ;
DEGOUYON, B ;
LAUTHIER, V ;
SILVER, LM ;
DAUSSET, J ;
CANN, HM ;
SPIELMAN, RS .
GENOMICS, 1992, 12 (04) :826-828
[8]   A NOVEL FAMILY OF HUMAN MAJOR HISTOCOMPATIBILITY COMPLEX-RELATED GENES NOT MAPPING TO CHROMOSOME-6 [J].
CALABI, F ;
MILSTEIN, C .
NATURE, 1986, 323 (6088) :540-543
[9]   Retinoic acid early inducible genes define a ligand family for the activating NKG2D receptor in mice [J].
Cerwenka, A ;
Bakker, ABH ;
McClanahan, T ;
Wagner, J ;
Wu, J ;
Phillips, JH ;
Lanier, LL .
IMMUNITY, 2000, 12 (06) :721-727
[10]   Ligands for natural killer cell receptors: redundancy or specificity [J].
Cerwenka, A ;
Lanier, LL .
IMMUNOLOGICAL REVIEWS, 2001, 181 :158-169