首页> 外文期刊>Comparative biochemistry and physiology, Part B. Biochemistry & molecular biology >Chitin deacetylase 1 and 2 are indispensable for larval-pupal and pupal-adult molts in Heortia vitessoides (Lepidoptera: Crambidae)
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Chitin deacetylase 1 and 2 are indispensable for larval-pupal and pupal-adult molts in Heortia vitessoides (Lepidoptera: Crambidae)

机译:甲壳素脱乙酰酶1和2对于草皮菌毒素(Lepidoptera:Crambidae)是必不可少的幼虫蛹和蛹成人蜕皮是必不可少的

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Heortia vitessoides Moore is a notorious defoliator of Aquilaria sinensis (Lour.) Gilg trees. Chitin deacetylases (CDAs) catalyze the N-deacetylation of chitin, which is a crucial process for chitin modification. Here, we identified and characterized HvCDA1 and HvCDA2 from H. vitessoides. HvCDA1 and HvCDA2 possess typical domain structures of CDAs and belong to the Group I CDAs. HvCDA1 and HvCDA2 were highly expressed before and after the larval-larval molt. In addition, both exhibited relatively high mRNA expression levels during the larval-pupal molt, the pupal stage, and the pupal-adult molt. HvCDA1 and HvCDA2 transcript expression levels were highest in the body wall and relatively high in the larval head. Significant increases in the HvCDA1 and HvCDA2 transcript expression levels were observed in the larvae upon exposure to 20-hydroxyecdysone. RNA interference-mediated HvCDA1 and HvCDA2 silencing significantly inhibited HvCDA1 and HvCDA2 expression, with abnormal or nonviable phenotypes being observed. Post injection survival rates of the larvae injected with dsHvCDA1 and dsHvCDA2 were 66.7% and 46.7% (larval-pupal) during development and 23.0% and 6.7% (pupal-adult), respectively. These rates were significantly lower than those of the control group insects. Our results suggest that HvCDA1 and HvCDA2 play important roles in the larval-pupal and pupal-adult transitions and represent potential targets for the management of H. vitessoides.
机译:Heortia Vitessoides Moore是Aquilaria Sinensis(Lour。)吉尔格树的臭名昭着的落叶剂。几丁质脱乙酰酶(CDAs)催化甲壳素的N-脱乙酰化,这是几丁质修饰的关键方法。在此,我们从H.Vitessoides识别和表征HVCDA1和HVCDA2。 HVCDA1和HVCDA2具有CDA的典型结构域结构,属于I CDAS。 HVCDA1和HVCDA2在幼虫幼虫蜕皮之前和之后高度表达。此外,两者在幼虫蛹蜕皮,蛹阶段和蛹 - 成人蜕皮中表现出相对高的mRNA表达水平。 HVCDA1和HVCDA2转录表达水平在体壁中最高,幼虫头部相对较高。在暴露于20-羟基迪克松时,在幼虫中观察到HVCDA1和HVCDA2转录表达水平的显着增加。 RNA干扰介导的HVCDA1和HVCDA2沉默显着抑制HVCDA1和HVCDA2表达,观察到异常或不可行的表型。在开发期间注射DSHVCDA1和DSHVCDA2的幼虫的后注射率分别为66.7%和46.7%(幼虫蛹),分别为23.0%和6.7%(蛹成人)。这些率明显低于对照组昆虫的速率。我们的研究结果表明,HVCDA1和HVCDA2在幼虫蛹和蛹 - 成年转换中起重要作用,并表示H. Vitestoides管理的潜在目标。

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