In situ hybridization analysis of immunoglobulin heavy chain variable gene expression with family specific oligonucleotide probes

被引:4
|
作者
Rundle, CH
Schroeder, HW
Koopman, WJ
机构
[1] Univ Alabama Birmingham, Dept Med, Chairmans Off, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Birmingham Vet Adm Med Ctr, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
关键词
in situ hybridization; oligonucleotide probes; B cells; heavy chain variable gene family;
D O I
10.1016/S0022-1759(98)00097-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have developed an improved in situ hybridization (ISH) technique for the analysis of human immunoglobulin heavy chain variable (V-H) gene family expression in suspensions of human B lymphocytes. Oligonucleotide probes specific for framework region (FR) consensus germline sequences for each of the seven human V-H gene families were designed and hybridization conditions were developed to accommodate the greatest degree of V-H gene variation, maximize the sensitivity of transcript detection, and assure the specificity of the technique. The hybridization parameters were rigorously characterized by Southern hybridization to a panel of 30 V-H cDNA clones and by ISH to 17 B cell Lines expressing characterized V-H genes. Results obtained with ISH using V-H gene family and isotype-specific gene probes correlated well with histochemical measures of Ig gene product expression. Profiles of cellular V-H gene expression were generated for mitogen stimulated peripheral blood B lymphocytes from six normal subjects. When compared with estimates of frequency of V-H genes in the human germline, the results were consistent with a random pattern of V-H family utilization. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:31 / 52
页数:22
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