Parker K L, Chaplin D D, Wong M, Seidman J G, Smith J A, Schimmer B P
Proc Natl Acad Sci U S A. 1985 Dec;82(23):7860-4. doi: 10.1073/pnas.82.23.7860.
The S region of the murine major histocompatibility complex contains two structurally related genes (21-OHase A and 21-OHase B) that encode 21-hydroxylase (21-OHase), an enzyme essential for the synthesis of adrenal steroids. Expression of these two genes has been analyzed by using oligonucleotide probes specific for the 21-OHase A and B genes and by DNA-mediated gene transfer. Hybridization of the oligonucleotides to blots of BALB/c adrenal RNA demonstrated that all 21-OHase mRNA is derived from the 21-OHase A gene. Cosmids bearing either the 21-OHase A or B gene were introduced into Y1 adrenocortical tumor cells by cotransfection with pSV2-neo. Cells transfected with the 21-OHase A gene expressed 21-OHase as determined by steroid metabolism and by RNA blot hybridization; 21-OHase transcripts were not detected in parent Y1 cells or in cells transfected with the 21-OHase B gene. Treatment of 21-OHase A transfectants with adrenocorticotropin increased 21-OHase mRNA levels by up to 10-fold, thus mimicking the observed effect of this hormone on 21-OHase levels in primary adrenal cultures. The regulated expression of the 21-OHase A gene in transfected Y1 cells should provide a useful system for the investigation of factors controlling the adrenal-specific regulation of 21-OHase activity.
小鼠主要组织相容性复合体的S区域包含两个结构相关的基因(21-羟化酶A和21-羟化酶B),它们编码21-羟化酶,这是肾上腺类固醇合成所必需的一种酶。通过使用针对21-羟化酶A和B基因的寡核苷酸探针以及DNA介导的基因转移,对这两个基因的表达进行了分析。寡核苷酸与BALB/c肾上腺RNA印迹杂交表明,所有21-羟化酶mRNA均来自21-羟化酶A基因。携带21-羟化酶A或B基因的黏粒通过与pSV2-neo共转染被导入Y1肾上腺皮质肿瘤细胞。用类固醇代谢和RNA印迹杂交法测定,转染了21-羟化酶A基因的细胞表达21-羟化酶;在亲本Y1细胞或转染了21-羟化酶B基因的细胞中未检测到21-羟化酶转录本。用促肾上腺皮质激素处理21-羟化酶A转染细胞,可使21-羟化酶mRNA水平提高多达10倍,从而模拟了该激素对原代肾上腺培养物中21-羟化酶水平的观察到的影响。21-羟化酶A基因在转染的Y1细胞中的调节表达应为研究控制21-羟化酶活性肾上腺特异性调节的因素提供一个有用的系统。