Dalet C, Clair P, Daujat M, Fort P, Blanchard J M, Maurel P
INSERM U 128, CNRS, Montpellier, France.
DNA. 1988 Jan-Feb;7(1):39-46. doi: 10.1089/dna.1988.7.39.
Two cDNAs (pLM3c 4.1 and pLM3c 6.1) coding for rabbit cytochrome P450 3c were sequenced. cDNA 4.1 (1768 bp) exhibits an open reading frame from nucleotides 74 to 1576 encoding the 501 amino acid residues of the entire protein. cDNA 6.1 (189 bp) appears to encode the last 24 amino acids. Comparative amino acid sequence analysis indicated that P450 PCN1, PCN2, and HLp from rat and man, were 70, 67, and 73% homologous, respectively, to P450 3c. According to the cytochrome P450 nomenclature, the P450 3c gene is termed P450IIIA4. Comparison of the nucleotide sequences indicated that cDNA 6.1 was 100% homologous to cDNA 4.1. However, whereas a poly(A) tract started 23 nucleotides after the AATAAA consensus sequence in cDNA 6.1, cDNA 4.1 had a 3' untranslated region extending 101 bp beyond the polyadenylation signal, which lacked poly(A). This observation is consistent with the previous finding that both cDNA 4.1 and 6.1 hybridized with two distinct species of poly(A)RNA (1700 and 1850 bases) from rabbit liver. The extreme 3'-end 79-bp fragment of cDNA 4.1 therefore was isolated by subcloning in pUC12 (clone p18-Rsa I) and used to probe Northern blots of poly(A)RNA from control and rifampicin-treated rabbit liver. In contrast to cDNA 4.1 and 6.1, p18-Rsa I cDNA hybridized only with the largest (1850 bases) mRNA species. We conclude that rabbit liver contains two P450 3c mRNA species differing in the length of their 3' untranslated region.
对两个编码兔细胞色素P450 3c的cDNA(pLM3c 4.1和pLM3c 6.1)进行了测序。cDNA 4.1(1768 bp)在核苷酸74至1576处呈现一个开放阅读框,编码整个蛋白质的501个氨基酸残基。cDNA 6.1(189 bp)似乎编码最后24个氨基酸。氨基酸序列比较分析表明,大鼠和人的P450 PCN1、PCN2和HLp与P450 3c的同源性分别为70%、67%和73%。根据细胞色素P450命名法,P450 3c基因被命名为P450IIIA4。核苷酸序列比较表明,cDNA 6.1与cDNA 4.1的同源性为100%。然而,虽然在cDNA 6.1中,多聚腺苷酸序列在AATAAA共有序列后23个核苷酸处开始,而cDNA 4.1有一个3'非翻译区,在多聚腺苷酸化信号之外延伸101 bp,且该区域缺乏多聚腺苷酸。这一观察结果与之前的发现一致,即cDNA 4.1和6.1都与来自兔肝脏的两种不同种类的多聚腺苷酸RNA(1700和1850个碱基)杂交。因此,通过亚克隆到pUC12中(克隆p18 - Rsa I)分离出cDNA 4.1的最末端3'端79 - bp片段,并用于探测对照和利福平处理的兔肝脏多聚腺苷酸RNA的Northern印迹。与cDNA 4.1和6.1不同,p18 - Rsa I cDNA仅与最大的(1850个碱基)mRNA种类杂交。我们得出结论,兔肝脏含有两种P450 3c mRNA种类,其3'非翻译区长度不同。