Sloan J H, Boss J M
Department of Microbiology and Immunology, Emory University, Atlanta, GA.
Proc Natl Acad Sci U S A. 1988 Nov;85(21):8186-90. doi: 10.1073/pnas.85.21.8186.
Class II major histocompatibility genes contain a conserved upstream sequence (CUS) that is important in the expression of these genes. This region has been divided into two major elements, the X box and the Y box. The ability of these elements to mediate transcription of a heterologous promoter was assayed upon transfection into a B-cell line (Raji), a class II-specific trans-acting factor-deficient B-cell line (RJ2.2.5 cells), and a T-cell line (Jurkat). The results showed that the X box element was responsible for directing tissue-specific expression when Raji cells were compared to Jurkat cells. The X box could not direct expression of the heterologous promoter in the trans-acting factor-deficient cell line, indicating that the X box is an ultimate target of the missing or defective factor in the RJ2.2.5 cell line. The Y box directed an equal but extremely low level of transcription in this system in both the mutant and wild-type B-cell lines, suggesting that this element is not involved in B-cell expression or as a target of the mutant factor.
II类主要组织相容性基因包含一个保守的上游序列(CUS),该序列对这些基因的表达很重要。该区域已被分为两个主要元件,即X框和Y框。将这些元件转染到B细胞系(拉吉细胞)、II类特异性反式作用因子缺陷的B细胞系(RJ2.2.5细胞)和T细胞系( Jurkat细胞)中,检测它们介导异源启动子转录的能力。结果表明,与Jurkat细胞相比,当拉吉细胞时,X框元件负责指导组织特异性表达。X框不能在反式作用因子缺陷的细胞系中指导异源启动子的表达,这表明X框是RJ2.2.5细胞系中缺失或缺陷因子的最终靶点。在该系统中,Y框在突变型和野生型B细胞系中均指导相同但极低水平的转录,这表明该元件不参与B细胞表达,也不是突变因子的靶点。