TY - JOUR
T1 - Evolutionary dynamics of the human immunoglobulin κ locus and the germline repertoire of the Vκ genes
AU - Kawasaki, Kazuhiko
AU - Minoshima, Shinsei
AU - Nakato, Eriko
AU - Shibuya, Kazunori
AU - Shintani, Ai
AU - Asakawa, Shuichi
AU - Sasaki, Takashi
AU - Klobeck, H. Gustav
AU - Combriato, Gabriele
AU - Zachau, Hans G.
AU - Shimizu, Nobuyoshi
PY - 2001
Y1 - 2001
N2 - We have determined the entire nucleotide sequence of the human immunoglobulin κ locus, comprising a total of 1,010,706 nucleotides. The 76 Vκ genes found by a hybridization-based approach and their classification in 7 families were confirmed. A Vκ orphon located near the locus was also sequenced. In addition, we identified 55 novel Vκ relics and truncated pseudogenes, which establish 5 new families. Among these 132 Vκ genes, 46 have open reading frames. According to the databases and the literature, 32 unique Vκ genes and 5 identical gene pairs form VJ-joints, 27 unique genes and 4 gene pairs are transcribed, and 25 unique genes and 4 gene pairs produce functional proteins. The Vκ gene locus contains a 360-kb inverted duplication, which harbors 118 Vκ genes. A comparison of the duplicated Vκ genes suggests positive selection on the complementarity-determining regions of the duplicated genes by point mutations. The entire duplication unit was divided into 13 blocks, each of which has its distinct nucleotide sequence identity to its duplication counterpart (98.1-99.9%). An inversion-mediated mechanism is suggested to generate the high-homology blocks. Based on the homology blocks and the mutation rates, the inverted duplication is assumed to have taken place ∼ 5 million years ago. An orphon Vκ gene near the κ locus and a cluster of five Vκ orphons on chromosome 22 have no counterparts within the κ locus. This suggests possible mechanisms of the transposition of orphon Vκ genes.
AB - We have determined the entire nucleotide sequence of the human immunoglobulin κ locus, comprising a total of 1,010,706 nucleotides. The 76 Vκ genes found by a hybridization-based approach and their classification in 7 families were confirmed. A Vκ orphon located near the locus was also sequenced. In addition, we identified 55 novel Vκ relics and truncated pseudogenes, which establish 5 new families. Among these 132 Vκ genes, 46 have open reading frames. According to the databases and the literature, 32 unique Vκ genes and 5 identical gene pairs form VJ-joints, 27 unique genes and 4 gene pairs are transcribed, and 25 unique genes and 4 gene pairs produce functional proteins. The Vκ gene locus contains a 360-kb inverted duplication, which harbors 118 Vκ genes. A comparison of the duplicated Vκ genes suggests positive selection on the complementarity-determining regions of the duplicated genes by point mutations. The entire duplication unit was divided into 13 blocks, each of which has its distinct nucleotide sequence identity to its duplication counterpart (98.1-99.9%). An inversion-mediated mechanism is suggested to generate the high-homology blocks. Based on the homology blocks and the mutation rates, the inverted duplication is assumed to have taken place ∼ 5 million years ago. An orphon Vκ gene near the κ locus and a cluster of five Vκ orphons on chromosome 22 have no counterparts within the κ locus. This suggests possible mechanisms of the transposition of orphon Vκ genes.
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U2 - 10.1002/1521-4141(200104)31:4<1017::AID-IMMU1017>3.0.CO;2-3
DO - 10.1002/1521-4141(200104)31:4<1017::AID-IMMU1017>3.0.CO;2-3
M3 - Article
C2 - 11298326
AN - SCOPUS:0035061129
SN - 0014-2980
VL - 31
SP - 1017
EP - 1028
JO - European Journal of Immunology
JF - European Journal of Immunology
IS - 4
ER -