Nakajima P B, Di Vincenzo J P, Jameson S C, Gascoigne N R
Department of Pathology, Fox Chase Cancer Center, Philadephia, PA 19111.
Immunogenetics. 1992;35(3):190-8. doi: 10.1007/BF00185113.
Analysis of mouse Tcr genes has previously defined at least five different Tcra-V haplotypes among inbred strains of mice. For mice of the Tcra-Vb haplotype, including C57BL/10 (B10), T-cell expression of the Tcra-V11 gene subfamily can be detected with a monoclonal antibody, 1.F2. In the course of further characterizing the specificity of 1.F2, we found that it fails to recognize Tcra-V11-expressing T-cell hybrids derived from the B10 congenic strain, B10.A(18R)/SgIcr. Moreover, staining analysis indicated that the Va11 epitope recognized by 1.F2 is not expressed by peripheral T cells from several different B10.A(18R) colonies with the exception of that at the Research Institute of Scripps Clinic. Nucleotide sequences were determined for cDNA representing rearranged Tcra-V11 genes from two independent, B10.A(18R)/SgIcr derived T-cell hybrids. The two Tcra-V11 gene segments were identical and the predicted amino acid sequence differed by at least five residues from Tcra-V11 sequences previously obtained from B10.A mice. Southern blot analysis of restriction fragment length polymorphisms (RFLP) associated with Tcra-V11, as well as Tcra-V1, subfamily genes revealed that the B10.A(18R) mouse has inherited Tcra-Va alleles rather than the expected Tcra-Vb alleles from the B10 strain. RFLP analysis of the Rib-1 locus, located in close proximity to the Tcra locus on chromosome 14, showed that B10.A(18R) carries the Rib-1b allele from B10. These results indicate that the B10.A(18R) mouse has inherited a recombinant chromosome 14 with a recombination event having occurred between the Rib-1 locus and the Tcra-V gene subfamilies examined. Inheritance of Tcra-Va alleles in B10.A(18R) probably originated from strain 129/J which breeding records show was used in the first cross with B10.A in the production of B10.A(18R) and which we found exhibits Tcra-V11a RFLPs.
对小鼠Tcr基因的分析先前已在近交系小鼠中确定了至少五种不同的Tcra-V单倍型。对于Tcra-Vb单倍型的小鼠,包括C57BL/10(B10),可用单克隆抗体1.F2检测Tcra-V11基因亚家族的T细胞表达。在进一步表征1.F2特异性的过程中,我们发现它无法识别源自B10同源系B10.A(18R)/SgIcr的表达Tcra-V11的T细胞杂交体。此外,染色分析表明,除了斯克里普斯诊所研究所的外周T细胞外,1.F2识别的Va11表位在来自几个不同B10.A(18R)菌落的外周T细胞中不表达。测定了代表来自两个独立的、源自B10.A(18R)/SgIcr的T细胞杂交体重排的Tcra-V11基因的cDNA的核苷酸序列。这两个Tcra-V11基因片段相同,预测的氨基酸序列与先前从B10.A小鼠获得的Tcra-V11序列至少相差五个残基。与Tcra-V11以及Tcra-V1亚家族基因相关的限制性片段长度多态性(RFLP)的Southern印迹分析表明,B10.A(18R)小鼠从B10品系继承了Tcra-Va等位基因而非预期的Tcra-Vb等位基因。对位于14号染色体上与Tcra基因座紧邻的Rib-1基因座的RFLP分析表明,B10.A(18R)携带来自B10的Rib-1b等位基因。这些结果表明,B10.A(18R)小鼠继承了一条重组的14号染色体,在Rib-1基因座和所检测的Tcra-V基因亚家族之间发生了重组事件。B10.A(18R)中Tcra-Va等位基因的继承可能源自129/J品系,繁殖记录显示该品系在B10.A(18R)的生产中与B10.A的首次杂交中被使用,并且我们发现其表现出Tcra-V11a RFLP。