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苏云金芽胞杆菌敏感和抗性品系对甘蔗螟中肠三种氨肽酶 N 同工酶的分子特征和 RNA 干扰。

Molecular characterization and RNA interference of three midgut aminopeptidase N isozymes from Bacillus thuringiensis-susceptible and -resistant strains of sugarcane borer, Diatraea saccharalis.

机构信息

Department of Entomology, Louisiana State University Agricultural Center, Baton Rouge, LA 70803, USA.

出版信息

Insect Biochem Mol Biol. 2010 Aug;40(8):592-603. doi: 10.1016/j.ibmb.2010.05.006. Epub 2010 Jun 2.

Abstract

Aminopeptidase N (APN) proteins located at the midgut epithelium of some lepidopteran species have been implicated as receptors for insecticidal proteins from Bacillus thuringiensis. cDNAs of three APN isoforms, DsAPN1, DsAPN2, and DsAPN3, from Cry1Ab-susceptible (Cry1Ab-SS) and -resistant (Cry1Ab-RR) strains of the sugarcane borer, Diatraea saccharalis (F.) (Lepidoptera: Crambidae), were identified and sequenced using reverse transcriptase polymerase chain reaction (RT-PCR) and 5' rapid amplification of cDNA end (5' RACE). The characteristic APN sequence features were derived from deduced amino acid sequences of the cloned cDNAs. cDNA sequences of the three APN genes were identical between the Cry1Ab-SS and -RR strains. However, total APN proteolytic activity and gene expression of the three APNs from Cry1Ab-RR larvae were significantly lower than those of the Cry1Ab-SS strain. RNA interference (RNAi) was employed using an oral droplet feeding technique for the three APNs of the Cry1Ab-SS strain. Down-regulating expressions of the three APN genes by RNAi were corresponding to the reductions in the specific APN activity. In addition, silencing of all three APNs in D. saccharalis in vivo by RNAi resulted in a decrease in Cry1Ab susceptibility. Our results showed that reduction in expression of the three APNs is functionally associated with the Cry1Ab resistance in D. saccharalis.

摘要

位于某些鳞翅目昆虫中肠上皮的氨肽酶 N (APN) 蛋白已被认为是苏云金芽孢杆菌杀虫蛋白的受体。从 Cry1Ab 敏感(Cry1Ab-SS)和抗性(Cry1Ab-RR)品系的甘蔗螟(Diatraea saccharalis(F.))中鉴定并测序了三种 APN 同工型的 cDNA,DsAPN1、DsAPN2 和 DsAPN3,使用逆转录聚合酶链反应(RT-PCR)和 5'快速扩增 cDNA 末端(5' RACE)。从克隆的 cDNA 推导的氨基酸序列得出了特征性的 APN 序列特征。三种 APN 基因的 cDNA 序列在 Cry1Ab-SS 和 -RR 品系之间是相同的。然而,来自 Cry1Ab-RR 幼虫的三种 APN 的总 APN 蛋白水解活性和基因表达明显低于 Cry1Ab-SS 品系。使用口服滴注技术对 Cry1Ab-SS 品系的三种 APN 进行了 RNA 干扰(RNAi)。通过 RNAi 下调三种 APN 基因的表达与特定 APN 活性的降低相对应。此外,通过 RNAi 在体内沉默 D. saccharalis 中的三种 APN 导致 Cry1Ab 敏感性降低。我们的结果表明,三种 APN 的表达减少与 D. saccharalis 中的 Cry1Ab 抗性在功能上相关。

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