Reith W, Satola S, Sanchez C H, Amaldi I, Lisowska-Grospierre B, Griscelli C, Hadam M R, Mach B
Department of Microbiology, University of Geneva Medical School, Switzerland.
Cell. 1988 Jun 17;53(6):897-906. doi: 10.1016/s0092-8674(88)90389-3.
The expression of MHC class II genes is tightly regulated. One form of congenital severe combined immunodeficiency (SCID) is characterized by a regulatory defect that precludes expression of HLA class II genes. B lymphocyte cell lines from such SCID patients provide a tool for identifying putative regulatory proteins that bind to class II gene promoters. We have identified three proteins binding to specific segments of the HLA-DRA promoter, two of which interact to form the predominant DNA-protein complex observed. One of these proteins, defined as an X box binding protein (RF-X), is specifically missing in cells from class II deficient SCID patients. We propose that the molecular defect in this congenital HLA class II regulatory deficiency is a lack of RF-X and that this factor plays an important role in the normal regulation of MHC class II gene expression.
MHC II类基因的表达受到严格调控。先天性严重联合免疫缺陷(SCID)的一种形式的特征是存在一种调节缺陷,该缺陷会阻止HLA II类基因的表达。来自此类SCID患者的B淋巴细胞系为鉴定与II类基因启动子结合的假定调节蛋白提供了一种工具。我们已经鉴定出三种与HLA-DRA启动子的特定片段结合的蛋白质,其中两种相互作用形成了观察到的主要DNA-蛋白质复合物。这些蛋白质之一,被定义为X盒结合蛋白(RF-X),在II类缺陷SCID患者的细胞中特异性缺失。我们提出,这种先天性HLA II类调节缺陷的分子缺陷是缺乏RF-X,并且该因子在MHC II类基因表达的正常调节中起重要作用。