Germain R N, Bentley D M, Quill H
Cell. 1985 Nov;43(1):233-42. doi: 10.1016/0092-8674(85)90028-5.
Cell surface Ia expression was examined following transfection of murine alpha and beta class II major histocompatibility complex (MHC) genes into L cells. Although haplotype-matched (e.g., Ak beta Ak alpha) gene pairs yielded high expression in primary transfectants, haplotype-mismatched pairs (e.g., Ak beta Ad alpha) gave unexpectedly low expression. RNA analysis revealed a requirement for greater A beta, and particularly A alpha transcript levels in haplotype-mismatched vs. haplotype-matched transfectants with similar levels of membrane Ia. A beta allelic control of this assembly/expression process was mapped to the NH2-terminal (beta 1) domain, the locus of high intraspecies polymorphism. These data on the effects of allelic variation on Ia levels provide a possible explanation for the strong linkage disequilibrium of A alpha and A beta genes and may account for the current molecular organization of the I region of the MHC.
在将小鼠α和β类II型主要组织相容性复合体(MHC)基因转染到L细胞后,检测了细胞表面Ia的表达。尽管单倍型匹配的(例如,AkβAkα)基因对在原代转染子中产生高表达,但单倍型不匹配的对(例如,AkβAdα)表达却出乎意料地低。RNA分析显示,与具有相似膜Ia水平的单倍型匹配转染子相比,单倍型不匹配转染子需要更高的Aβ,尤其是Aα转录水平。这种组装/表达过程的Aβ等位基因控制被定位到NH2末端(β1)结构域,即种内高度多态性的位点。这些关于等位基因变异对Ia水平影响的数据为Aα和Aβ基因的强连锁不平衡提供了一种可能的解释,并可能解释了MHC I区目前的分子组织。