Germline transcription and switch recombination of a transgene containing the entire H chain constant region locus:: Effect of a mutation in a STAT6 binding site in the γ1 promoter

被引:19
作者
Dunnick, WA [1 ]
Shi, J [1 ]
Graves, KA [1 ]
Collins, JT [1 ]
机构
[1] Univ Michigan, Sch Med, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
关键词
D O I
10.4049/jimmunol.173.9.5531
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The switch (S) in H chain class is preceded by germline transcription and then mediated by a DNA recombination event. One of the impediments toward understanding the mechanism is the lack of a system in which a recombinant DNA molecule undergoes cytokine-regulated class S recombination. To study class S recombination, we used transgenic mice with a 230-kb bacterial artificial chromosome that included a rearranged VDJ gene and the entire murine H chain constant region locus. We found that both germline transcription and S recombination to the transgenic gamma1 H chain gene were regulated by IL-4 like that of the endogenous genes. In mice with two or more copies of the H chain locus transgene, both germline transcripts and S. recombination took place at levels comparable to those from the endogenous loci. We also prepared a version of the transgene with a 4-bp mutation in a STAT6 binding site in the gamma1 promoter region. On the average, this mutation reduced germline transcription by 80%, but did not change the amount of S recombination in vitro. Among both the wild-type and mutant transgenes, we found no significant correlation between the amount of germline transcripts and the amount of S recombination. We infer that the physiologic level of germline transcription of the gamma1 gene is in excess over the amount required for efficient S recombination.
引用
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页码:5531 / 5539
页数:9
相关论文
共 66 条
[21]   Bcl-2 obstructs negative selection of autoreactive, hypermutated antibody V regions during memory B cell development [J].
Hande, S ;
Notidis, E ;
Manser, T .
IMMUNITY, 1998, 8 (02) :189-198
[22]   Processing of switch transcripts is required for targeting of antibody class switch recombination [J].
Hein, K ;
Lorenz, MGO ;
Siebenkotten, G ;
Petry, K ;
Christine, R ;
Radbruch, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (12) :2369-2374
[23]   Level of B cell antigen receptor surface expression influences both positive and negative selection of B cells during primary development [J].
Heltemes, LM ;
Manser, T .
JOURNAL OF IMMUNOLOGY, 2002, 169 (03) :1283-1292
[24]  
Hogan B., 1994, MANIPULATING MOUSE E
[26]  
HUMMEL M, 1987, J IMMUNOL, V138, P3539
[27]   DNA-BINDING SITES 5' OF THE IGG1 SWITCH REGION COMPRISING IL4 INDUCIBILITY AND B-CELL SPECIFICITY [J].
ILLGES, H ;
RADBRUCH, A .
MOLECULAR IMMUNOLOGY, 1992, 29 (10) :1265-1272
[28]   REQUIREMENT OF TYROSINE PHOSPHORYLATION FOR RAPID ACTIVATION OF A DNA-BINDING FACTOR BY IL-4 [J].
KOTANIDES, H ;
REICH, NC .
SCIENCE, 1993, 262 (5137) :1265-1267
[29]   Quantitative regulation of class switch recombination by switch region transcription [J].
Lee, CG ;
Kinoshita, K ;
Arudchandran, A ;
Cerritelli, SM ;
Crouch, RJ ;
Honjo, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (03) :365-373
[30]   REGULATION AND TARGETING OF RECOMBINATION IN EXTRACHROMOSOMAL SUBSTRATES CARRYING IMMUNOGLOBULIN SWITCH REGION SEQUENCES [J].
LEUNG, H ;
MAIZELS, N .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (02) :1450-1458