Buhler D R, Yang Y H, Dreher T W, Miranda C L, Wang J L
Department of Agricultural Chemistry, Oregon State University, Corvallis 97331.
Arch Biochem Biophys. 1994 Jul;312(1):45-51. doi: 10.1006/abbi.1994.1278.
We have cloned and sequenced a full-length cDNA encoding the major constitutive rainbow trout liver cytochrome P450 that we had earlier designated as cytochrome P450 LMC2 (Arch. Biochem. Biophys. 268, 227, 1989). The 1859-bp cDNA was isolated from a male rainbow trout liver cDNA library and contained an open reading frame encoding for a protein of 504 amino acids and having a calculated molecular weight of 56,795. From nucleotide and amino acid sequence comparisons, the trout P450 LMC2 has been assigned to a new cytochrome P450 gene subfamily designated P4502K1 or CYP2K1. Marked differences in the sex- and tissue-specific expression of this gene were found at both the transcriptional and translational level in sexually mature rainbow trout liver and trunk kidney. Transcriptional expression investigated by Northern analysis of total RNA using a 440-bp 3'-terminal cDNA probe (2K1,7c) showed sexual and organ differences. Mature male trunk kidney expressed 2K1,7c-hybridizable mRNA to a substantially greater extent than did female trunk kidney, with multiple mRNA bands appearing in approximately the 2.8- and 1.9-kb region. While the livers of some males displayed separate 2.8-kb hybridizable bands, such bands were generally undetectable in female liver samples. By contrast, 1.9-kb mRNA bands were found at generally similar concentrations in the livers of both sexes. Taking into consideration the individual biological variabilities, it was apparent that mature male trout expressed the 2.8-kb mRNA much more strongly in trunk kidney than in liver. Translational expression, analyzed by Western blotting of microsomes separated on sodium dodecyl sulfate-polyacrylamide gel electrophoresis and probed with rabbit polyclonal antibody and two different monoclonal antibodies prepared against P450 LMC2, demonstrated corresponding sex- and organ-related differences in P450 protein expression. Southern analysis of sexually mature male trout genomic DNA suggested that CYP2K1 is not a single copy gene, thus providing additional evidence for the complexity of the CYP2K1 system in rainbow trout.
我们已经克隆并测序了一个全长cDNA,它编码虹鳟鱼肝脏中主要的组成型细胞色素P450,我们之前将其命名为细胞色素P450 LMC2(《生物化学与生物物理学报》268, 227, 1989)。这个1859 bp的cDNA是从雄性虹鳟鱼肝脏cDNA文库中分离出来的,包含一个开放阅读框,编码一个由504个氨基酸组成的蛋白质,计算分子量为56,795。通过核苷酸和氨基酸序列比较,虹鳟鱼的P450 LMC2被归入一个新的细胞色素P450基因亚家族,命名为P4502K1或CYP2K1。在性成熟的虹鳟鱼肝脏和肾中,该基因在转录和翻译水平上的性别和组织特异性表达存在显著差异。使用440 bp的3'-末端cDNA探针(2K1,7c)对总RNA进行Northern分析来研究转录表达,结果显示存在性别和器官差异。成熟雄性肾中表达2K1,7c可杂交mRNA的程度明显高于雌性肾,在大约2.8 kb和1.9 kb区域出现多条mRNA条带。虽然一些雄性的肝脏显示出单独的2.8 kb可杂交条带,但在雌性肝脏样本中通常检测不到这些条带。相比之下,1.9 kb的mRNA条带在两性肝脏中的浓度通常相似。考虑到个体生物学差异,很明显成熟雄性虹鳟鱼在肾中表达2.8 kb mRNA的强度远高于肝脏。通过对十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳分离的微粒体进行Western印迹分析,并使用兔多克隆抗体和针对P450 LMC2制备的两种不同单克隆抗体进行检测,分析翻译表达,结果表明P450蛋白表达存在相应的性别和器官相关差异。对性成熟雄性虹鳟鱼基因组DNA进行Southern分析表明,CYP2K1不是单拷贝基因,从而为虹鳟鱼中CYP2K1系统的复杂性提供了额外证据。