Harper K, Mattéi M G, Simon D, Suzan M, Guénet J L, Haddad P, Sasportes M, Golstein P
Centre d'Immunologie, INSERM-CNRS de Marseille-Luminy, France.
Immunogenetics. 1988;28(6):439-44. doi: 10.1007/BF00355376.
The serine esterase CTLA-1 gene was shown by in situ hybridization to map to the D segment of mouse chromosome 14, the same localization as a member of the immunoglobulin superfamily, Tcr alpha. To further demonstrate the proximity of CTLA-1 and Tcr alpha, genetic linkage was tested in mouse using restriction fragment length polymorphisms and a backcross progeny, and no recombination was observed in the 100 backcross products studied. Recombination events between Tcr alpha/CTLA-1 and the markers Gdh-X and NP-1 show that the most probable order of these loci in the mouse 14D region is NP-1-Tcr alpha/Ctla-1-Gdh-X. In man, the human homologue of CTLA-1 was shown by in situ hybridization to map on chromosome 14, at 14q11-q12, where Tcr alpha also maps. Using the human cell line SUP-T1, bearing the inversion inv(14) (q11;q32), we further demonstrated the loci order in man to be centromere-NP-1-Tcr alpha-CTLA-1. To complement the cytogenetic and genetic mapping data, we tried to determine the physical distance between the two genes by pulsed field gel electrophoresis (PFGE). DNA prepared from various cell types, both mouse and human, were digested with a panel of rare cutter enzymes and hybridized first with CTLA-1, then with Tcr alpha probes. None of the bands identified hybridized with both Tcr alpha and CTLA-1 probes for either mouse or human cells. Although the physical mapping by PFGE is inconclusive, the cytogenetic and genetic data support close linkage of the Tcr alpha and CTLA-1 genes in both mouse and man, suggesting homology between the D region of mouse chromosome 14 and the q11-q12 region of human chromosome 14, encompassing the Tcr alpha and CTLA-1 loci. These findings also provide another example of proximity of genes coding for a member of the Ig super-family and a serine esterase.
通过原位杂交显示,丝氨酸酯酶CTLA-1基因定位于小鼠14号染色体的D区段,与免疫球蛋白超家族成员Tcrα的定位相同。为了进一步证明CTLA-1和Tcrα的邻近性,利用限制性片段长度多态性和回交后代在小鼠中进行了遗传连锁测试,在所研究的100个回交产物中未观察到重组。Tcrα/CTLA-1与标记Gdh-X和NP-1之间的重组事件表明,这些基因座在小鼠14D区域中最可能的顺序是NP-1-Tcrα/Ctla-1-Gdh-X。在人类中,通过原位杂交显示CTLA-1的人类同源物定位于14号染色体的14q11-q12,Tcrα也定位于此。利用携带inv(14)(q11;q32)倒位的人类细胞系SUP-T1,我们进一步证明人类中的基因座顺序为着丝粒-NP-1-Tcrα-CTLA-1。为了补充细胞遗传学和遗传图谱数据,我们试图通过脉冲场凝胶电泳(PFGE)确定这两个基因之间的物理距离。从小鼠和人类的各种细胞类型中制备的DNA用一组稀有切割酶消化,首先与CTLA-1杂交,然后与Tcrα探针杂交。对于小鼠或人类细胞,所鉴定的条带均未与Tcrα和CTLA-1探针同时杂交。尽管通过PFGE进行的物理图谱分析尚无定论,但细胞遗传学和遗传数据支持Tcrα和CTLA-1基因在小鼠和人类中紧密连锁,这表明小鼠14号染色体的D区域与人类14号染色体的q11-q12区域具有同源性,该区域包含Tcrα和CTLA-1基因座。这些发现也提供了另一个编码Ig超家族成员的基因与丝氨酸酯酶基因邻近的例子。