Hegan Peter S, Mermall Valerie, Tilney Lewis G, Mooseker Mark S
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06520, USA.
Mol Biol Cell. 2007 Nov;18(11):4625-36. doi: 10.1091/mbc.e07-02-0191. Epub 2007 Sep 12.
Drosophila myosin IB (Myo1B) is one of two class I myosins in the Drosophila genome. In the larval and adult midgut enterocyte, Myo1B is present within the microvillus (MV) of the apical brush border (BB) where it forms lateral tethers between the MV membrane and underlying actin filament core. Expression of green fluorescent protein-Myo1B tail domain in the larval gut showed that the tail domain is sufficient for localization of Myo1B to the BB. A Myo1B deletion mutation exhibited normal larval gut physiology with respect to food uptake, clearance, and pH regulation. However, there is a threefold increase in terminal deoxynucleotidyl transferase dUTP nick-end labeling-positive enterocyte nuclei in the Myo1B mutant. Ultrastructural analysis of mutant midgut revealed many perturbations in the BB, including membrane tethering defects, MV vesiculation, and membrane shedding. The apical localization of both singed (fascin) and Dmoesin is impaired. BBs isolated from mutant and control midgut revealed that the loss of Myo1B causes the BB membrane and underlying cytoskeleton to become destabilized. Myo1B mutant larvae also exhibit enhanced sensitivity to oral infection by the bacterial pathogen Pseudomonas entomophila, and severe cytoskeletal defects are observed in the BB of proximal midgut epithelial cells soon after infection. Resistance to P. entomophila infection is restored in Myo1B mutant larvae expressing a Myo1B transgene. These results indicate that Myo1B may play a role in the local midgut response pathway of the Imd innate immune response to Gram-negative bacterial infection.
果蝇肌球蛋白IB(Myo1B)是果蝇基因组中两种I类肌球蛋白之一。在幼虫和成虫中肠肠上皮细胞中,Myo1B存在于顶端刷状缘(BB)的微绒毛(MV)内,在那里它在MV膜和下面的肌动蛋白丝核心之间形成侧向连接。绿色荧光蛋白-Myo1B尾部结构域在幼虫肠道中的表达表明,尾部结构域足以使Myo1B定位于BB。Myo1B缺失突变体在食物摄取、清除和pH调节方面表现出正常的幼虫肠道生理功能。然而,在Myo1B突变体中,末端脱氧核苷酸转移酶dUTP缺口末端标记阳性的肠上皮细胞核增加了三倍。突变体中肠的超微结构分析显示BB存在许多扰动,包括膜连接缺陷、MV囊泡化和膜脱落。singed(fascin)和Dmoesin的顶端定位均受损。从突变体和对照中肠分离的BB显示,Myo1B的缺失导致BB膜和下面的细胞骨架变得不稳定。Myo1B突变体幼虫对细菌病原体嗜虫假单胞菌的口服感染也表现出增强的敏感性,并且在感染后不久,近端中肠上皮细胞的BB中观察到严重的细胞骨架缺陷。在表达Myo1B转基因的Myo1B突变体幼虫中,对嗜虫假单胞菌感染的抗性得以恢复。这些结果表明,Myo1B可能在Imd先天免疫反应对革兰氏阴性细菌感染的局部中肠反应途径中发挥作用。