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Duox 在果蝇翅膀稳定中的重要作用。

Essential role of Duox in stabilization of Drosophila wing.

机构信息

Department of Applied Biology, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan.

出版信息

J Biol Chem. 2011 Sep 23;286(38):33244-51. doi: 10.1074/jbc.M111.263178. Epub 2011 Jul 30.

Abstract

NADPH oxidase produces reactive oxygen species (ROS). Drosophila melanogaster has two homologs of NADPH oxidase, dNox and dDuox, with functions that remain unclear in vivo. To clarify these functions, two independent transgenic fly lines expressing dsRNA targeted for different portions of dDuox mRNA were used. In both flies, en-GAL4> UAS-dDuoxIR(976-1145) and en-GAL4> UAS-dDuoxIR(370-518), in which dDuox was knocked down selectively in the posterior area of the wing disc, the posterior compartment of the adult wings became paler and more fragile with wing veins that were indistinct by comparison with the anterior one. Fluorescence staining of the en-GAL4> UAS-dDuoxIR(976-1145) adult wings revealed that the ROS concentration in the posterior compartment was significantly lower than that in the anterior compartment. Moreover, in these flies, the posterior compartment of the wing imaginal disc showed a greater number of apoptotic cells detected by immunostaining with anti-cleaved caspase-3 antibody than those in the anterior compartment. Respective knockdown of tyrosine hydroxylase or dopa-decarboxylase showed paler wing blades in the posterior compartment similar to the phenotype of dDuox-knockdown files. Along with this observation, analysis of the catecholic and dityrosine components in the wings of adult flies proved that dDuox plays important roles in the stabilization of the cuticle structure of the wings via tyrosine cross-linking, the sclerotization and melanization processes possibly through ROS production. These dDuox-knockdown fly lines would be useful tools for further studying dDuox functions during the development of Drosophila.

摘要

NADPH 氧化酶产生活性氧(ROS)。果蝇有两种 NADPH 氧化酶的同源物,dNox 和 dDuox,其体内功能尚不清楚。为了阐明这些功能,使用了两种独立的表达靶向 dDuox mRNA 不同部分的 dsRNA 的转基因果蝇系。在两种果蝇中,en-GAL4>UAS-dDuoxIR(976-1145)和 en-GAL4>UAS-dDuoxIR(370-518)中,dDuox 在翅膀盘的后区域被选择性敲低,与前区域相比,成年翅膀的后区域变得更苍白、更脆弱,翅膀静脉不明显。en-GAL4>UAS-dDuoxIR(976-1145)成年翅膀的荧光染色显示,后区域的 ROS 浓度明显低于前区域。此外,在这些果蝇中,与前区域相比,翅膀 imaginal 盘的后区域显示出更多的凋亡细胞,这些细胞通过抗 cleaved caspase-3 抗体免疫染色检测到。酪氨酸羟化酶或多巴脱羧酶的相应敲低导致后区域的翅膀更苍白,类似于 dDuox 敲低的表型。随着这一观察结果,对成年果蝇翅膀中儿茶酚和二酪氨酸成分的分析证明,dDuox 通过酪氨酸交联在稳定翅膀的外骨骼结构、硬化和黑化过程中(可能通过 ROS 产生)发挥重要作用。这些 dDuox 敲低的果蝇系将成为进一步研究果蝇发育过程中 dDuox 功能的有用工具。

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