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The elusive actin cytoskeleton of a green alga expressing both conventional and divergent actins

机译:表达常规和发散型肌动蛋白的绿藻的难以使用的肌动蛋白细胞骨架

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摘要

The green alga Chlamydomonas reinhardtii is a leading model system to study photosynthesis, cilia, and the generation of biological products. The cytoskeleton plays important roles in all of these cellular processes, but to date, the filamentous actin network within Chlamydomonas has remained elusive. By optimizing labeling conditions, we can now visualize distinct linear actin filaments at the posterior of the nucleus in both live and fixed vegetative cells. Using in situ cryo-electron tomography, we confirmed this localization by directly imaging actin filaments within the native cellular environment. The fluorescently labeled structures are sensitive to the depolymerizing agent latrunculin B (Lat B), demonstrating the specificity of our optimized labeling method. Interestingly, Lat B treatment resulted in the formation of a transient ring-like filamentous actin structure around the nucleus. The assembly of this perinuclear ring is dependent upon a second actin isoform, NAP1, which is strongly up-regulated upon Lat B treatment and is insensitive to Lat B-induced depolymerization. Our study combines orthogonal strategies to provide the first detailed visual characterization of filamentous actins in Chlamydomonas, allowing insights into the coordinated functions of two actin isoforms expressed within the same cell.
机译:绿地藻类衣原体Reinhardtii是一个领先的模型系统,用于研究光合作用,纤毛和生物产品的产生。细胞骨架在所有这些细胞过程中起重要作用,但到目前为止,衣原体内的丝状肌动蛋白网络仍然难以捉摸。通过优化标记条件,我们现在可以在Live和固定营养细胞中可视化核后部的不同线性肌动蛋白细胞。使用原位冷冻电子断层扫描,我们通过直接在本地细胞环境内直接映射肌动蛋白细丝来确认本地化。荧光标记的结构对解聚剂Latrunculin B(LAT B)敏感,证明了我们优化的标记方法的特异性。有趣的是,LAT B治疗导致在细胞核周围形成瞬态环状丝状肌动蛋白结构。该细胞环的组装取决于第二肌动蛋白同种型,NAP1,其在LAT B处理时强烈地调节,对LAT B诱导的解聚不敏感。我们的研究结合了正交的策略,提供了粉碎中的丝状肌动蛋白的第一次详细目视表征,允许在同一细胞中表达的两种肌动蛋白同种型的协调功能中的见解。

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