Tine J A, Walsh A, Rathbun D, Leonard L, Wakeland E K, Dilwith R, Flaherty L
Wadsworth Center for Laboratories and Research, Albany, NY 12201.
Immunogenetics. 1990;31(5-6):315-25. doi: 10.1007/BF02115005.
Both serological and DNA sequence analyses were performed to determine the extent of genetic polymorphism in Q region genes. A panel of Qa-2-specific monoclonal antibodies (mAbs) was tested on 35 wild-derived and inbred mouse strains. Members of this reagent panel recognize multiple and distinct epitopes on the Qa-2-bearing molecule(s). Although quantitative variations in Qa-2 levels were observed, no structural polymorphisms were detected. All strains were either entirely positive or entirely negative with the complete set of reagents. Moreover, cell surface Qa-2 expression was not significantly affected by differences in age or sex of the mouse or cell cycle status. To confirm this apparent lack of genetic polymorphism, the polymerase chain reaction (PCR) technique was used to amplify a portion of the 3' end of the Q region genes, Q4 to Q9, from several independent wild-derived strains of mice. Sequence analysis of the amplified material revealed very little evidence of nucleotide divergence. All strains tested had a Q even DNA sequence identical to that of Q6/Q8 in the B10 strain. Likewise, all tested strains had a Q odd DNA sequence identical to Q7/Q9 in the B10 strain. Two strains showed additional Q even sequences, while all strains tested possessed additional Q odd sequences. The observed lack of polymorphism suggests that the Q genes have evolved in a different manner from H-2K and H-2D. Moreover, duplications of these genes appear to have arisen prior to nucleotide sequence divergence.
为了确定Q区域基因的遗传多态性程度,我们进行了血清学和DNA序列分析。使用一组Qa - 2特异性单克隆抗体(mAb)对35种野生来源和近交系小鼠品系进行了检测。该试剂组的成员识别携带Qa - 2分子上的多个不同表位。虽然观察到Qa - 2水平存在定量差异,但未检测到结构多态性。所有品系对整套试剂要么完全呈阳性,要么完全呈阴性。此外,小鼠的年龄或性别差异以及细胞周期状态对细胞表面Qa - 2表达没有显著影响。为了证实这种明显的遗传多态性缺失,我们使用聚合酶链反应(PCR)技术从几个独立的野生来源小鼠品系中扩增Q区域基因3'端的一部分,即Q4至Q9。对扩增产物的序列分析显示几乎没有核苷酸差异的证据。所有测试品系的Q偶数DNA序列与B10品系中的Q6 / Q8相同。同样,所有测试品系的Q奇数DNA序列与B10品系中的Q7 / Q9相同。两个品系显示出额外的Q偶数序列,而所有测试品系都具有额外的Q奇数序列。观察到的多态性缺失表明Q基因的进化方式与H - 2K和H - 2D不同。此外,这些基因的重复似乎在核苷酸序列分歧之前就已经出现。