Analysis of mutational lineage trees from sites of primary and secondary Ig gene diversification in rabbits and chickens

被引:27
作者
Mehr, R
Edelman, H
Sehgal, D
Mage, R
机构
[1] Bar Ilan Univ, Fac Life Sci, IL-52900 Ramat Gan, Israel
[2] Natl Inst Immunol, Mol Immunol Grp, New Delhi, India
[3] NIAID, Immunogenet Mol Lab, Immunol Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.4049/jimmunol.172.8.4790
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lineage trees of mutated rearranged Ig V region sequences in B lymphocyte clones often serve to qualitatively illustrate claims concerning the dynamics of affinity maturation. In this study, we use a novel method for analyzing lineage tree shapes, using terms from graph theory to quantify the differences between primary and secondary diversification in rabbits and chickens. In these species, Ig gene diversification starts with rearrangement of a single (in chicken) or a few (in rabbit) V-H genes. Somatic hypermutation and gene conversion contribute to primary diversification in appendix of young rabbits or in bursa of Fabricius of embryonic and young chickens and to secondary diversification during immune responses in germinal centers (GCs). We find that, at least in rabbits, primary diversification appears to occur at a constant rate in the appendix, and the type of Ag-specific selection seen in splenic GCs is absent. This supports the view that a primary repertoire is being generated within the expanding clonally related B cells in appendix of young rabbits and emphasizes the important role that gut-associated lymphoid tissues may play in early development of mammalian immune repertoires. Additionally, the data indicate a higher rate of hypermutation in rabbit and chicken GCs, such that the balance between hypermutation and selection tends more toward mutation and less toward selection in rabbit and chicken compared with murine GCs.
引用
收藏
页码:4790 / 4796
页数:7
相关论文
共 58 条
[1]   ANTIBODY ENGINEERING FOR THE ANALYSIS OF AFFINITY MATURATION OF AN ANTI-HAPTEN RESPONSE [J].
ALLEN, D ;
SIMON, T ;
SABLITZKY, F ;
RAJEWSKY, K ;
CUMANO, A .
EMBO JOURNAL, 1988, 7 (07) :1995-2001
[2]   Immunoglobulin gene hyperconversion ongoing in chicken splenic germinal centers [J].
Arakawa, H ;
Furusawa, S ;
Ekino, S ;
Yamagishi, H .
EMBO JOURNAL, 1996, 15 (10) :2540-2546
[3]  
Arakawa H, 1998, J IMMUNOL, V160, P4232
[4]   Effect of environmental antigens on the Ig diversification and the selection of productive V-J joints in the bursa [J].
Arakawa, H ;
Kuma, K ;
Yasuda, M ;
Ekino, S ;
Shimizu, A ;
Yamagishi, H .
JOURNAL OF IMMUNOLOGY, 2002, 169 (02) :818-828
[5]  
Banerjee M, 2002, EUR J IMMUNOL, V32, P1947, DOI 10.1002/1521-4141(200207)32:7<1947::AID-IMMU1947>3.0.CO
[6]  
2-1
[7]  
Barington T, 1996, J IMMUNOL, V157, P4016
[8]   Survival and clonal expansion of mutating "forbidden" (immunoglobulin receptor-deficient) Epstein-Barr virus-infected B cells in angioimmunoblastic T cell lymphoma [J].
Bräuninger, A ;
Spieker, T ;
Willenbrock, K ;
Gaulard, P ;
Wacker, HH ;
Rajewsky, K ;
Hansmann, ML ;
Küppers, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (07) :927-940
[9]   Somatic immunoglobulin hypermutation [J].
Diaz, M ;
Casali, P .
CURRENT OPINION IN IMMUNOLOGY, 2002, 14 (02) :235-240
[10]  
DOMER T, 1998, IMMUNOL REV, V162, P161