Chaplin D D, Galbraith L J, Seidman J G, White P C, Parker K L
Proc Natl Acad Sci U S A. 1986 Dec;83(24):9601-5. doi: 10.1073/pnas.83.24.9601.
Steroid 21-hydroxylase [21-OHase; steroid 21-monooxygenase; steroid, hydrogen-donor:oxygen oxidoreductase (21-hydroxylating); EC 1.14.99.10] is a cytochrome P-450 enzyme required for the adrenal synthesis of mineralocorticoids and glucocorticoids. The gene encoding this protein is present in two copies (21-OHase A and B) in the S region of the murine major histocompatibility complex. Previous studies utilizing gene-specific oligonucleotide probes and gene transfer showed that only the 21-OHase A gene is expressed in the BALB/c mouse. Here, we present the complete primary structures of both BALB/c 21-OHase encoding genes. Comparison of the nucleotide sequences defines a deletion of 215 nucleotides spanning the second exon of the 21-OHase B gene; other nucleotide changes in the 21-OHase B gene introduce frame shifts and premature termination codons. Southern blot analysis of C57BL/6 and DBA/2J mice indicates that a similar deletion is present in these strains; however the C3H/HeJ strain is a structural variant. A hybrid gene composed of the 21-OHase B promoter placed 5' of the 21-OHase A structural sequences was efficiently transcribed following transfection into Y1 adrenocortical tumor cells. These findings demonstrate that the 21-OHase B gene promoter is functional and suggest that mutations within the 21-OHase B structural gene are responsible for its lack of expression.
类固醇21 -羟化酶[21 - OHase;类固醇21 -单加氧酶;类固醇,氢供体:氧氧化还原酶(21 -羟化);EC 1.14.99.10]是肾上腺合成盐皮质激素和糖皮质激素所需的一种细胞色素P - 450酶。编码该蛋白的基因在小鼠主要组织相容性复合体的S区域以两个拷贝形式存在(21 - OHase A和B)。先前利用基因特异性寡核苷酸探针和基因转移进行的研究表明,只有21 - OHase A基因在BALB/c小鼠中表达。在此,我们展示了BALB/c 21 - OHase两个编码基因的完整一级结构。核苷酸序列比较确定了21 - OHase B基因第二个外显子跨度为215个核苷酸的缺失;21 - OHase B基因中的其他核苷酸变化引入了移码和提前终止密码子。对C57BL/6和DBA/2J小鼠的Southern印迹分析表明,这些品系中存在类似的缺失;然而,C3H/HeJ品系是一种结构变体。一个由21 - OHase B启动子置于21 - OHase A结构序列5'端组成的杂合基因在转染到Y1肾上腺皮质肿瘤细胞后被有效转录。这些发现证明21 - OHase B基因启动子具有功能,并表明21 - OHase B结构基因内的突变是其缺乏表达的原因。