Antigen-receptor genes of the agnathan lamprey are assembled by a process involving copy choice

被引:121
作者
Nagawa, Fumikiyo [1 ]
Kishishita, Natsuko
Shimizu, Kazumichi
Hirose, Satoshi
Miyoshi, Masato
Nezu, Junnya
Nishimura, Toshinobu
Nishizumi, Hirofumi
Takahashi, Yoshimasa
Hashimoto, Shu-ichi
Takeuchi, Masaki
Miyajima, Atsushi
Takemori, Toshitada
Otsuka, Anthony J.
Sakano, Hitoshi
机构
[1] Univ Tokyo, Grad Sch Sci, Dept Biophys & Biochem, Bunkyo Ku, Tokyo 1130032, Japan
[2] Natl Int Infect Dis, Shinjuku Ku, Tokyo 1628640, Japan
[3] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
[4] Illinois State Univ, Dept Biol Sci, Normal, IL 61790 USA
关键词
D O I
10.1038/ni1419
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Jawless vertebrates have acquired immunity but do not have immunoglobulin-type antigen receptors. Variable lymphocyte receptors (VLRs) have been identified in lamprey that consist of multiple leucine-rich repeat (LRR) modules. An active VLR gene is generated by the assembly of a series of variable gene segments, including many that encode LRRs. Stepwise assembly of the gene segments seems to occur by replacement of the intervening DNA between the 5' and 3' constant-region genes. Here we report that lamprey (Lethenteron japonicum) assemble their VLR genes by a process involving 'copy choice'. Regions of short homology seemed to prime copying of donor LRR-encoding sequences into the recipient gene. Those LRR-encoding germline sequences were abundant and shared extensive sequence homologies. Such genomic organization permits initiation of copying anywhere in an LRR-encoding module for the generation of various hybrid LRRs. Thus, a vast repertoire of recombinant VLR genes could be generated not only by copying of various LRR segments in diverse combinations but also by the use of multiple sites in an LRR gene segment for priming.
引用
收藏
页码:206 / 213
页数:8
相关论文
共 40 条
[1]   Pathogen recognition and innate immunity [J].
Akira, S ;
Uematsu, S ;
Takeuchi, O .
CELL, 2006, 124 (04) :783-801
[2]   Diversity and function of adaptive immune receptors in a jawless vertebrate [J].
Alder, MN ;
Rogozin, IB ;
Iyer, LM ;
Glazko, GV ;
Cooper, MD ;
Pancer, Z .
SCIENCE, 2005, 310 (5756) :1970-1973
[3]   Immunoglobulin gene conversion: Insights from bursal B cells and the DT40 cell line [J].
Arakawa, H ;
Buerstedde, JM .
DEVELOPMENTAL DYNAMICS, 2004, 229 (03) :458-464
[4]   Fission yeast switches mating type by a replication-recombination coupled process [J].
Arcangioli, B ;
de Lahondès, R .
EMBO JOURNAL, 2000, 19 (06) :1389-1396
[5]  
Barry JD, 2005, BIOCHEM SOC T, V33, P986, DOI 10.1042/BST20050986
[6]   Leucine-rich repeats and pathogen recognition in Toll-like receptors [J].
Bell, JK ;
Mullen, GED ;
Leifer, CA ;
Mazzoni, A ;
Davies, DR ;
Segal, DM .
TRENDS IN IMMUNOLOGY, 2003, 24 (10) :528-533
[7]   Antigenic variation and allelic exclusion [J].
Borst, P .
CELL, 2002, 109 (01) :5-8
[8]   Antigenic variation of Anaplasma marginale msp2 occurs by combinatorial gene conversion [J].
Brayton, KA ;
Palmer, GH ;
Lundgren, A ;
Yi, J ;
Barbet, AF .
MOLECULAR MICROBIOLOGY, 2002, 43 (05) :1151-1159
[9]   The phylogenetic origins of the antigen-binding receptors and somatic diversification mechanisms [J].
Cannon, JP ;
Haire, RN ;
Rast, JP ;
Litman, GW .
IMMUNOLOGICAL REVIEWS, 2004, 200 :12-22
[10]   The evolution of adaptive immune systems [J].
Cooper, MD ;
Alder, MN .
CELL, 2006, 124 (04) :815-822