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γ-Actin is required for cytoskeletal maintenance but not development

机译:γ-肌动蛋白是维持细胞骨架所必需的而不是发育所需的

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摘要

βcyto-Actin and γcyto-actin are ubiquitous proteins thought to be essential building blocks of the cytoskeleton in all non-muscle cells. Despite this widely held supposition, we show that γcyto-actin null mice (Actg1−/−) are viable. However, they suffer increased mortality and show progressive hearing loss during adulthood despite compensatory up-regulation of βcyto-actin. The surprising viability and normal hearing of young Actg1−/− mice means that βcyto-actin can likely build all essential non-muscle actin-based cytoskeletal structures including mechanosensory stereocilia of hair cells that are necessary for hearing. Although γcyto-actin–deficient stereocilia form normally, we found that they cannot maintain the integrity of the stereocilia actin core. In the wild-type, γcyto-actin localizes along the length of stereocilia but re-distributes to sites of F-actin core disruptions resulting from animal exposure to damaging noise. In Actg1−/− stereocilia similar disruptions are observed even without noise exposure. We conclude that γcyto-actin is required for reinforcement and long-term stability of F-actin–based structures but is not an essential building block of the developing cytoskeleton.
机译:β细胞肌动蛋白和γ细胞肌动蛋白是普遍存在的蛋白质,被认为是所有非肌肉细胞中细胞骨架的重要组成部分。尽管存在这种普遍存在的假设,但我们证明γ细胞-肌动蛋白无效小鼠(Actg1 -/-)是可行的。然而,尽管β细胞肌动蛋白代偿性上调,但它们的死亡率却增加,并且在成年期表现出进行性听力丧失。年轻的Actg1 -// 小鼠令人惊讶的生存力和正常听力意味着β-细胞肌动蛋白可以构建所有必需的非肌肉肌动蛋白基细胞骨架结构,包括听力所必需的毛细胞的机械感性立体纤毛。尽管缺乏γ-肌动蛋白的立体纤毛正常形成,但我们发现它们不能保持立体纤毛肌动蛋白核心的完整性。在野生型中,γ-细胞肌动蛋白沿着立体纤毛的长度定位,但重新分布在F-肌动蛋白核心破坏的部位,这种破坏是由于动物暴露于有害噪音而引起的。在Actg1 -/-立体纤毛中,即使没有噪声暴露,也会观察到类似的破坏。我们得出的结论是,γ-肌动蛋白是增强基于F-肌动蛋白的结构和使其长期稳定所必需的,但它并不是发育中的细胞骨架的重要组成部分。

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