在黑腹果蝇中,Torr的功能障碍导致了一种丑角型鱼鳞病样表型

Y. Wang, M. Norum, K. Oehl, Y. Yang, R. Zuber, J. Yang, J. Farine, N. Gehring, M. Flötenmeyer, J. Ferveur, B. Moussian
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GFP-tagged Torr localises to membrane nano-protrusions within the cuticle, likely pore canals. This suggests that Torr is mediating the transport of cuticular hydrocarbons (CHC) through the pore canals to the cuticle surface. The envelope, which is the outermost cuticle layer constituting the main barrier, is unaffected in torr mutant larvae. This contrasts with the function of Snu, another ABC transporter needed for the construction of the cuticular inward and outward barriers, that nevertheless is implicated in CHC deposition. Hence, Torr and Snu have overlapping and independent roles to establish cuticular resistance against transpiration and xenobiotic penetration. The torr deficient phenotype parallels the phenotype of Harlequin ichthyosis caused by mutations in the human abca12 gene. Thus, it seems that the cellular and molecular mechanisms of lipid barrier assembly in the skin are conserved in vertebrates in invertebrates. 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引用次数: 0

摘要

防止干燥对陆生生物来说是一个持续的挑战。陆生昆虫有一层细胞外的皮毛,即角质层,它在防止水分过度流失方面起着重要作用。在这里,我们报道了ABC转运蛋白Torr——一种人类ABCA12的类似物——有助于果蝇表皮的防水屏障功能。我们表明,托尔函数的减少或消除会引起快速干燥。Torr还参与了对外来生物渗透的内部屏障的定义。与此一致的是,当Torr活性降低时,参与角质层抗渗性的角质层碳氢化合物的数量显著减少。gfp标记的Torr定位于角质层内的膜纳米突起,可能是孔管。这表明Torr通过孔管介导角质层碳氢化合物(CHC)向角质层表面的运输。包膜是构成主要屏障的最外层角质层,在torr突变体幼虫中不受影响。这与Snu的功能形成对比,Snu是另一种ABC转运蛋白,用于构建角质层内向和外向屏障,但与CHC沉积有关。因此,Torr和Snu在建立抗蒸腾和外来生物渗透的角质层抗性方面具有重叠和独立的作用。torr缺陷表型与人类abca12基因突变引起的Harlequin鱼鳞病表型相似。因此,皮肤脂质屏障组装的细胞和分子机制似乎在脊椎动物和无脊椎动物中是保守的。与人类一样,昆虫皮肤表面的脂质保护生物体免受过多的水分流失和潜在有害物质的渗透。在进化过程中,油腻的表面确实是适应水外环境的基本特征。在这里,我们展示了膜门转运体Torr是通过细胞外纳米管(称为孔管)在果蝇皮肤表面沉积屏障脂质的需要。原则上,Torr的参与与人类的情况相似,其中膜门转运蛋白ABCA12与皮肤脂质角质层的构建有关。在这两种情况下,编码各自转运体的基因突变会导致水分迅速流失,并且在出生后不久就会致命。我们的结论是,生物和环境之间的相互作用显然暗示了屏障形成和功能在脊椎动物和无脊椎动物中的类似机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dysfunction of Torr causes a Harlequin-type ichthyosis-like phenotype in Drosophila melanogaster
Prevention of desiccation is a constant challenge for terrestrial organisms. Land insects have an extracellular coat, the cuticle, that plays a major role in protection against exaggerated water loss. Here, we report that the ABC transporter Torr - a human ABCA12 paralog - contributes to the waterproof barrier function of the cuticle in the fruit fly Drosophila melanogaster. We show that the reduction or elimination of Torr function provokes rapid desiccation. Torr is also involved in defining the inward barrier against xenobiotics penetration. Consistently, the amounts of cuticular hydrocarbons that are involved in cuticle impermeability decrease markedly when Torr activity is reduced. GFP-tagged Torr localises to membrane nano-protrusions within the cuticle, likely pore canals. This suggests that Torr is mediating the transport of cuticular hydrocarbons (CHC) through the pore canals to the cuticle surface. The envelope, which is the outermost cuticle layer constituting the main barrier, is unaffected in torr mutant larvae. This contrasts with the function of Snu, another ABC transporter needed for the construction of the cuticular inward and outward barriers, that nevertheless is implicated in CHC deposition. Hence, Torr and Snu have overlapping and independent roles to establish cuticular resistance against transpiration and xenobiotic penetration. The torr deficient phenotype parallels the phenotype of Harlequin ichthyosis caused by mutations in the human abca12 gene. Thus, it seems that the cellular and molecular mechanisms of lipid barrier assembly in the skin are conserved in vertebrates in invertebrates. Author Summary As in humans, lipids on the surface of the skin of insects protect the organism against excessive water loss and penetration of potentially harmful substances. During evolution, a greasy surface was indeed an essential trait for adaptation to life outside a watery environment. Here, we show that the membrane-gate transporter Torr is needed for the deposition of barrier lipids on the skin surface in the fruit fly Drosophila melanogaster through extracellular nano-tubes, called pore canals. In principle, the involvement of Torr parallels the scenario in humans, where the membrane-gate transporter ABCA12 is implicated in the construction of the lipid-based stratum corneum of the skin. In both cases, mutations in the genes coding for the respective transporter cause rapid water-loss and are lethal soon after birth. We conclude that the interaction between the organism and the environment obviously implies an analogous mechanism of barrier formation and function in vertebrates and invertebrates.
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