Identification, characterization, and expression of a novel P450 gene encoding CYP6AE25 from the Asian corn borer, Ostrinia furnacalis
文献类型: 外文期刊
作者: Zhang, Yu-liang 1 ; Kulye, Mahesh 2 ; Yang, Feng-shan 3 ; Xiao, Luo 4 ; Zhang, Yi-tong 3 ; Zeng, Hong-mei 2 ; Wang, Ji 1 ;
作者机构: 1.Chinese Acad Trop Agr Sci, Minist Agr, Inst Trop Biosci & Biotechnol, Haikou 571101, Hainan, Peoples R China
2.Chinese Acad Agr Sci, Inst Plant Protect, Minist Agr, Key Lab Biol Control, Beijing 100081, Peoples R China
3.Heilongjiang Univ, Coll Life Sci, Key Lab Heilongjiang Microbiol, Harbin 150080, Heilongjiang, Peoples R China
4.Hunan Agr Univ, Coll Biosafety Sci & Technol, Changsha 410128, Hunan, Peoples R China
关键词: cytochrome P450;real-time PCR;bioinformatics
期刊名称:JOURNAL OF INSECT SCIENCE ( 影响因子:1.857; 五年影响因子:1.904 )
ISSN: 1536-2442
年卷期: 2011 年 11 卷
页码:
收录情况: SCI
摘要: An allele of the cytochrome P450 gene, CYP6AE14, named CYP6AE25 (GenBank accession no. EU807990) was isolated from the Asian corn borer, Ostrinia furnacalis (Guenee) (Lepidoptera: Pyralidae) by RT-PCR. The cDNA sequence of CYP6AE25 is 2315 bp in length and contains a 1569 nucleotides open reading frame encoding a putative protein with 523 amino acid residues and a predicted molecular weight of 59.95 kDa and a theoretical pI of 8.31. The putative protein contains the classic heme-binding sequence motif F x x G x x x C x G (residues 451-460) conserved among all P450 enzymes as well as other characteristic motifs of all cytochrome P450s. It shares 52% identity with the previously published sequence of CYP6AE14 (GenBank accession no. DQ986461) from Helicoverpa armigera. Phylogenetic analysis of amino acid sequences from members of various P450 families indicated that CYP6AE25 has a closer phylogenetic relationship with CYP6AE14 and CYP6B1 that are related to metabolism of plant allelochemicals, CYP6D1 which is related to pyrethroid resistance and has a more distant relationship to CYP302A1 and CYP307A1 which are related to synthesis of the insect molting hormones. The expression level of the gene in the adults and immature stages of O. furnacalis by quantitative real-time PCR revealed that CYP6AE25 was expressed in all life stages investigated. The mRNA expression level in 3(rd) instar larvae was 12.8- and 2.97-fold higher than those in pupae and adults, respectively. The tissue specific expression level of CYP6AE25 was in the order of midgut, malpighian tube and fatty body from high to low but was absent in ovary and brain. The analysis of the CYP6AE25 gene using bioinformatic software is discussed.
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