The leukocyte receptor complex in chicken is characterized by massive expansion and diversification of immunoglobulin-like loci

被引:58
作者
Laun, Katja
Coggill, Penny
Palmer, Sophie
Sims, Sarah
Ning, Zemin
Ragoussis, Jiannis
Volpi, Emanuela
Wilson, Natalie
Beck, Stephan
Ziegler, Andreas
Volz, Armin
机构
[1] Humboldt Univ, Charite Univ Med Berlin, Inst Immungenet, D-1040 Berlin, Germany
[2] Wellcome Trust Sanger Inst, Cambridge, England
[3] Wellcome Trust Ctr Human Genet, Oxford, England
基金
英国惠康基金;
关键词
D O I
10.1371/journal.pgen.0020073
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The innate and adaptive immune systems of vertebrates possess complementary, but intertwined functions within immune responses. Receptors of the mammalian innate immune system play an essential role in the detection of infected or transformed cells and are vital for the initiation and regulation of a full adaptive immune response. The genes for several of these receptors are clustered within the leukocyte receptor complex (LRC). The purpose of this study was to carry out a detailed analysis of the chicken (Gallus gallus domesticus) LRC. Bacterial artificial chromosomes containing genes related to mammalian leukocyte immunoglobulin-like receptors were identified in a chicken genomic library and shown to map to a single microchromosome. Sequencing revealed 103 chicken immunoglobulin-like receptor (CHIR) loci (22 inhibitory, 25 activating, 15 bifunctional, and 41 pseudogenes). A very complex splicing pattern was found using transcript analyses and seven hypervariable regions were detected in the external CHIR domains. Phylogenetic and genomic analysis showed that CHIR genes evolved mainly by block duplications from an ancestral inhibitory receptor locus, with transformation into activating receptors occurring more than once. Evolutionary selection pressure has led not only to an exceptional expansion of the CHIR cluster but also to a dramatic diversification of CHIR loci and haplotypes. This indicates that CHIRs have the potential to complement the adaptive immune system in fighting pathogens.
引用
收藏
页码:707 / 718
页数:12
相关论文
共 64 条
[1]   A large database of chicken bursal ESTs as a resource for the analysis of vertebrate gene function [J].
Abdrakhmanov, I ;
Lodygin, D ;
Geroth, P ;
Arakawa, H ;
Law, A ;
Plachy, J ;
Korn, B ;
Buerstedde, JM .
GENOME RESEARCH, 2000, 10 (12) :2062-2069
[2]   Natural selection drives recurrent formation of activating killer cell immunoglobulin-like receptor and Ly49 from inhibitory homologues [J].
Abi-Rached, L ;
Parham, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (08) :1319-1332
[3]   At least one class I gene in restriction fragment pattern-Y (Rfp-Y), the second MHC gene cluster in the chicken, is transcribed, polymorphic, and shows divergent specialization in antigen binding region [J].
Afanassieff, M ;
Goto, RM ;
Ha, J ;
Sherman, MA ;
Zhong, LW ;
Auffray, C ;
Coudert, F ;
Zoorob, R ;
Miller, MM .
JOURNAL OF IMMUNOLOGY, 2001, 166 (05) :3324-3333
[4]   Specific recognition of virus-infected cells by paired NK receptors [J].
Arase, H ;
Lanier, LL .
REVIEWS IN MEDICAL VIROLOGY, 2004, 14 (02) :83-93
[5]   Role of amino acid position 70 in the binding affinity of p50.1 and p58.1 receptors for HLA-Cw4 molecules [J].
Biassoni, R ;
Pessino, A ;
Malaspina, A ;
Cantoni, C ;
Bottino, C ;
Sivori, S ;
Moretta, L ;
Moretta, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (12) :3095-3099
[6]   A comprehensive collection of chicken cDNAs [J].
Boardman, PE ;
Sanz-Ezquerro, J ;
Overton, IM ;
Burt, DW ;
Bosch, E ;
Fong, WT ;
Tickle, C ;
Brown, WRA ;
Wilson, SA ;
Hubbard, SJ .
CURRENT BIOLOGY, 2002, 12 (22) :1965-1969
[7]   Crystal structure of an NK cell immunoglobulin-like receptor in complex with its class I MHC ligand [J].
Boyington, JC ;
Motyka, SA ;
Schuck, P ;
Brooks, AG ;
Sun, PD .
NATURE, 2000, 405 (6786) :537-543
[8]   The LILR family: modulators of innate and adaptive immune pathways in health and disease [J].
Brown, D ;
Trowsdale, J ;
Allen, R .
TISSUE ANTIGENS, 2004, 64 (03) :215-225
[9]   Fast and sensitive multiple alignment of large genomic sequences -: art. no. 66 [J].
Brudno, M ;
Chapman, M ;
Göttgens, B ;
Batzoglou, S ;
Morgenstern, B .
BMC BIOINFORMATICS, 2003, 4 (1)
[10]   A novel phosphotyrosine motif with a critical amino acid at position-2 for the SH2 domain-mediated activation of the tyrosine phosphatase SHP-1 [J].
Burshtyn, DN ;
Yang, WT ;
Yi, TL ;
Long, EO .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (20) :13066-13072