RECIPROCAL HYBRID JOINTS DEMONSTRATE SUCCESSIVE V-J REARRANGEMENTS ON THE SAME CHROMOSOME IN THE HUMAN TCR GAMMA LOCUS

被引:14
作者
ALEXANDRE, D
CHUCHANA, P
RONCAROLO, MG
YSSEL, H
SPITS, H
LEFRANC, G
LEFRANC, MP
机构
[1] DNAX RES INST MOLEC & CELLULAR BIOL INC,MOLEC & CELL BIOL INC RES INST,PALO ALTO,CA 94304
[2] UNIV MONTPELLIER SCI & TECH LANGUEDOC 2,IMMUNOGENET MOLEC LAB,CNRS,URA 1191,PL E BATAILLON,F-34095 MONTPELLIER 5,FRANCE
关键词
T-CELL RECEPTOR; GAMMA-CHAIN; VARIABLE GENES; RECOMBINATION SIGNALS; RECOMBINASE; INVERSION;
D O I
10.1093/intimm/3.10.973
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Novel variable (V) - joining (J) gene rearrangements are described in the human T cell receptor gamma locus, in which, on the one hand, the V3 variable gene is joined to the heptamer - nonamer recombination signals of the J1 segment and, on the other hand, the J1 segment is joined to the V3 recombination signals through head-to-head fusion. These recombination products, or hybrid joints, have been originated through an inversion of 47 kb DNA. Interestingly the inverted DNA stretch contains a normal V9-JP rearrangement. These findings are the first direct demonstration that successive rearrangements occur, on the same chromosome, in the human T cell receptor gamma locus, and suggest that the chronology of the joining events plays a role in the ontogeny of T cells and their differentiation in gamma/delta+ and alpha/beta+ lineages.
引用
收藏
页码:973 / 982
页数:10
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