Ranasinghe C, Hobbs A A
Department of Biochemistry, University of Western Australia, Nedlands, Australia.
Insect Biochem Mol Biol. 1998 Aug;28(8):571-80. doi: 10.1016/s0965-1748(98)00045-9.
Two new cDNA clones specific for members of the CYP6B gene family, CYP6B6 and CYP6B7 have been isolated from Helicoverpa armigera. The sequences correspond to mRNAs of an estimated 1962 and 2411 nucleotides in length respectively excluding the poly A tails. The two mRNAs have open reading frames encoding proteins of 504 amino acid residues with molecular weights of 57,564 and 58,181 Daltons. Both putative proteins contain the conserved cysteine and surrounding regions characteristics of all cytochrome P450s. The encoded protein sequences show 84-88% protein sequence identity between them and with the previously published cytochrome P450 sequence of H. armigera. CYP6B2. The sequences of cDNA clones of CYP6B6 and CYP6B2 show a very high degree of identity within the first 340 nucleotides which may be the result of a gene conversion event. Two major bands are visible after northern analysis of larval RNA using cDNA clones for CYP6B6, CYP6B7, or the previously published CYP6B2 as probes, due to strong cross-hybridization. Analysis with specific oligonucleotide probes and 3' non-coding regions indicated that the cDNAs for CYP6B6 and CYP6B7 correspond to the smaller and large mRNA bands respectively. The previously identified sequence of CYP6B2, contrary to the previous suggestion, corresponds to a rare mRNA of similar size to that for CYP6B6. The mRNA for CYP6B7 was found to be induced by treatment with the monoterpene, alpha-pinene, and to be over-expressed in some individuals of pyrethroid resistant population of H. armigera. We suggest that CYP6B7 is the form responsible for pyrethroid metabolism in H. armigera.
已从棉铃虫中分离出两个对CYP6B基因家族成员具有特异性的新cDNA克隆,即CYP6B6和CYP6B7。这些序列分别对应于估计长度为1962和2411个核苷酸的mRNA,不包括多聚A尾。这两种mRNA具有开放阅读框,编码504个氨基酸残基的蛋白质,分子量分别为57,564和58,181道尔顿。两种推测的蛋白质均含有所有细胞色素P450所特有的保守半胱氨酸及周围区域。编码的蛋白质序列彼此之间以及与先前发表的棉铃虫细胞色素P450序列CYP6B2之间显示出84 - 88%的蛋白质序列同一性。CYP6B6和CYP6B2的cDNA克隆序列在前340个核苷酸内显示出非常高的同一性,这可能是基因转换事件的结果。使用CYP6B6、CYP6B7或先前发表的CYP6B2的cDNA克隆作为探针,对幼虫RNA进行Northern分析后,由于强烈的交叉杂交,可见两条主要条带。用特异性寡核苷酸探针和3'非编码区进行分析表明,CYP6B6和CYP6B7的cDNA分别对应于较小和较大的mRNA条带。与先前的推测相反,先前鉴定的CYP6B2序列对应于一种与CYP6B6大小相似的稀有mRNA。发现CYP6B7的mRNA可被单萜α-蒎烯诱导,并在棉铃虫拟除虫菊酯抗性种群的一些个体中过表达。我们认为CYP6B7是棉铃虫中负责拟除虫菊酯代谢的形式。