首页> 外文期刊>Comparative biochemistry and physiology, Part B. Biochemistry & molecular biology >Characterization and regulation of Bacillus thuringiensis Cry toxin binding aminopeptidases N (APNs) from non-gut visceral tissues, Malpighian tubule and salivary gland: Comparison with midgut-specific APN in the moth Achaea janata
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Characterization and regulation of Bacillus thuringiensis Cry toxin binding aminopeptidases N (APNs) from non-gut visceral tissues, Malpighian tubule and salivary gland: Comparison with midgut-specific APN in the moth Achaea janata

机译:非肠道内脏组织,马尔皮基小管和唾液腺中苏云金芽孢杆菌Cry毒素结合氨基肽酶N(APNs)的表征和调控:与蛾类小菜蛾中肠特异性APN的比较

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摘要

Bacillus thuringiensis (Bt) crystal proteins (Cry) bind to aminopeptidase N (APN) receptors on insect midgut membrane leading to pore formation and subsequent death. However, evolution of insect resistance to Bt toxins threatens their long-term application. Therefore, search for new targets which could function as Cry toxin receptors is an immediate mandate. In the present study, two full-length APN cDNAs were cloned from Malpighian tubule and salivary gland tissues of the moth, Achaea janata. Both these APNs showed 99% and 32% sequence homology with fat body and midgut APNs respectively. Tissue distribution analysis revealed the presence of two different APN isoforms, one predominant in non-gut visceral tissues while the other exclusively expressed in the midgut. Immunofluorescence and western blot analyses showed cross-reactivity in Malpighian tubule and salivary gland when probed with anti-fat body APN antiserum. These results clearly indicated the presence of non-gut (AjAPN1) and gut-specific (AjAPN4) isoforms in this moth. The expression of both the isoforms steadily increased during the larval development. Hormonal studies indicated regulation of the APN genes by the morphogenetic hormones, 20-hydroxyecdyone and juvenile hormone. Further, in vitro ligand-blotting studies demonstrated binding of Cry toxins to APNs in Malpighian tubule and salivary gland indicating their potential as alternate targets.
机译:苏云金芽孢杆菌(Bt)晶体蛋白(Cry)与昆虫中肠膜上的氨肽酶N(APN)受体结合,导致孔形成并随后死亡。但是,昆虫对Bt毒素的抗性演变威胁了它们的长期应用。因此,寻找可用作Cry毒素受体的新靶标是当务之急。在本研究中,从蛾的小管和唾液腺组织(Achaea janata)克隆了两个全长APN cDNA。这两种APNs均与脂肪体和中肠APNs分别显示99%和32%的序列同源性。组织分布分析显示存在两种不同的APN亚型,一种在非肠道内脏组织中占主导,而另一种仅在中肠中表达。免疫荧光和蛋白质印迹分析表明,当用抗脂体APN抗血清探测时,在Malpighian小管和唾液腺中有交叉反应。这些结果清楚地表明在这种飞蛾中存在非肠道(AjAPN1)和肠道特异性(AjAPN4)同工型。在幼虫发育期间,两种同工型的表达稳定增加。激素研究表明,形态发生激素,20-羟基蜕皮激素和少年激素对APN基因的调节。此外,体外配体印迹研究表明,Cal毒素与Malpighian肾小管和唾液腺中的APNs结合,表明它们有可能成为替代靶标。

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