Soloski M J, Oudshoorn-Snoek M, Einhorn G, Demant P
Division of Molecular and Clinical Rheumatology, Johns Hopkins School of Medicine, Baltimore, MD 21205.
J Immunol. 1989 Nov 1;143(9):3074-80.
The Qa-11 Ag expressed in certain strains with the B2-microglobulin-b allele, apparently maps into the Tla region as well as into the Qa-2 region. Moreover Qa-11 has been shown to be biochemically indistinguishable from Qa-2. Genetic complementation studies combining the right Qa and Tla regions failed to lead to Qa-11 expression. To elucidate the molecular basis of this apparent paradox, we examined the expression of Qa-11 on products of transfected Q-region class I genes. Immunochemical analysis has shown that the Qa-11 Ag is expressed on class I molecules encoded by the Q7 gene from both C57BL/10 (Q7b) and BALB/c (Q7d), but not on the protein product of the Q9 gene isolated from the C57BL/10 strain (Q9b). Inasmuch as the predicted protein products of the Q7b and Q9b genes would differ at a single amino acid, a residue critical for Qa-11 expression has been identified. Based on these results it is proposed that among the beta-2-mb strains, the Qa-11+/Qa-2+ mice are likely to express at least the Q7 gene, whereas Qa-11-/Qa-2+ mice express only Q9. In support of this model, the Qa-2+/Q-11- recombinant B6.K2, essential for the apparent mapping of Qa-11 into the Tla region, expresses only Q9 but not Q7 encoded molecules on the cell surface, and only Q9 and no processed Q7 mRNA is detected in the cytoplasm. This expression pattern in B6.K2 cannot be explained on the basis of a single crossing-over event.
在某些带有β2-微球蛋白b等位基因的品系中表达的Qa-11抗原,显然定位于Tla区域以及Qa-2区域。此外,已证明Qa-11在生化性质上与Qa-2无法区分。将正确的Qa和Tla区域进行遗传互补研究未能导致Qa-11表达。为了阐明这一明显矛盾的分子基础,我们检测了转染的Q区域I类基因产物上Qa-11的表达。免疫化学分析表明,Qa-11抗原在来自C57BL/10(Q7b)和BALB/c(Q7d)的Q7基因编码的I类分子上表达,但在从C57BL/10品系分离的Q9基因(Q9b)的蛋白质产物上不表达。由于Q7b和Q9b基因的预测蛋白质产物在单个氨基酸上存在差异,已鉴定出一个对Qa-11表达至关重要的残基。基于这些结果,有人提出在β2-微球蛋白b品系中,Qa-11+/Qa-2+小鼠可能至少表达Q7基因,而Qa-11-/Qa-2+小鼠仅表达Q9。为支持这一模型,对Qa-11明显定位于Tla区域至关重要的Qa-2+/Q-11-重组体B6.K2,在细胞表面仅表达Q9编码的分子而不表达Q7编码的分子,并且在细胞质中仅检测到Q9而未检测到加工后的Q7 mRNA。B6.K2中的这种表达模式不能基于单一的交叉事件来解释。