Tukey R H, Okino S, Barnes H, Griffin K J, Johnson E F
J Biol Chem. 1985 Oct 25;260(24):13347-54.
Rabbits exhibit phenotypic differences, 21H and 21L, in the rate of hepatic progesterone 21-hydroxylation that reflect 10-fold higher microsomal concentrations of cytochrome P-450 1 in 21H rabbits. A cDNA library in pBR322 was prepared from liver mRNA isolated from a 21H rabbit. A clone, p1-8, producing a hybrid protein resulting from the insertion of the cDNA into the beta-lactamase gene of the plasmid expressed 5 distinct epitopes that were recognized by a panel of monoclonal antibodies developed toward P-450 1. RNAs selected from total hepatic mRNA by filter hybridization with p1-8 yield at least two electrophoretically distinct proteins when translated in vitro and immunoprecipitated with the 3C3 monoclonal antibody. Only one of the two proteins is recognized by the 1F11 monoclonal antibody, which is highly specific for P-450 1, and the immunoprecipitated protein exhibits the electrophoretic mobility of P-450 1. The other protein remains unidentified. Northern blot analysis indicates that the 3' noncoding portion of p1-8 hybridizes to higher steady state concentrations of polyadenylated RNA in the 21H as compared to 21L rabbits. This correspondence in expression with that of P-450 1 in the 21H and 21L phenotypes further suggests that p1-8 encodes P-450 1 or a closely related protein. The cDNA is 1871 base pairs in length and encodes a protein of 487 amino acids. Southern blot analysis indicates that several independent, gene-like sequences hybridize with the 3' noncoding region of p1-8 under conditions of high stringency. These results indicate that P-450 1 is a member of an extensive multigene family.
兔子在肝脏孕酮21 - 羟化速率上表现出表型差异,即21H和21L,这反映出21H兔子微粒体中细胞色素P - 450 1的浓度比21L兔子高10倍。从一只21H兔子分离的肝脏mRNA制备了pBR322中的cDNA文库。一个克隆p1 - 8,将cDNA插入质粒的β - 内酰胺酶基因后产生一种杂交蛋白,该杂交蛋白表达了5个不同的表位,这些表位能被一组针对P - 450 1开发的单克隆抗体识别。通过与p1 - 8进行滤膜杂交从肝脏总mRNA中筛选出的RNA,在体外翻译并用3C3单克隆抗体进行免疫沉淀时,产生至少两种电泳上不同的蛋白质。这两种蛋白质中只有一种能被对P - 450 1高度特异的1F11单克隆抗体识别,并且免疫沉淀的蛋白质表现出P - 450 1的电泳迁移率。另一种蛋白质身份不明。Northern印迹分析表明,与21L兔子相比,p1 - 8的3'非编码部分与21H兔子中聚腺苷酸化RNA的更高稳态浓度杂交。在21H和21L表型中这种表达与P - 450 1的对应关系进一步表明p1 - 8编码P - 450 1或一种密切相关的蛋白质。该cDNA长度为1871个碱基对,编码一种487个氨基酸的蛋白质。Southern印迹分析表明,在高严谨度条件下,几个独立的、类似基因的序列与p1 - 8的3'非编码区域杂交。这些结果表明P - 450 1是一个广泛的多基因家族的成员。