MOLECULAR CHARACTERIZATION OF THE HUMAN IMMUNOGLOBULIN-V-GAMMA-I GERMLINE GENE REPERTOIRE

被引:31
作者
DALEY, MD
OLEE, T
PENG, HQ
SOTOGIL, RW
CHEN, PP
SIMINOVITCH, KA
机构
[1] UNIV TORONTO, MT SINAI HOSP,SAMUEL LUNENFELD RES INST, DEPT ANAESTHESIA,ROOM 656A,600 UNIV AVE, TORONTO M5G 1X5, ONTARIO, CANADA
[2] UNIV TORONTO, MT SINAI HOSP, SAMUEL LUNENFELD RES INST, DEPT IMMUNOL, TORONTO M5G 1X5, ONTARIO, CANADA
[3] UNIV TORONTO, MT SINAI HOSP, SAMUEL LUNENFELD RES INST, DEPT MED, TORONTO M5G 1X5, ONTARIO, CANADA
[4] UNIV CALIF SAN DIEGO, DEPT MED, LA JOLLA, CA 92093 USA
关键词
D O I
10.1016/0161-5890(92)90034-U
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To advance our understanding of the human immunoglobulin V-lambda germline gene contribution to normal as well as autoimmune responses, we have isolated and sequenced six germline genes of the V-lambda-I subgroup. These genes can be divided into three sub-subgroups on the basis of greater-than-or-equal-to 93% nucleotide sequence homology and greater-than-or-equal-to 88% deduced amino acid sequence similarity. Examination of all cDNA and protein sequences available for expressed V-lambda-I genes supports the assignment of these three sub-subgroups. Sequence comparisons also suggest that germline gene members of two of these sub-subgroups, I-a and I-b, are preferentially utilized in the expressed V-lambda-I repertoire. This finding may be at least partially attributable to regulatory sequence abnormalities apparent in two of the other V-lambda-I germline genes (Humlv101 and Humlv1041) which may interfere with their expression.
引用
收藏
页码:1031 / 1042
页数:12
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