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首页> 外文期刊>Eukaryotic cell >Clustering of Nuclei in Multinucleated Hyphae Is Prevented by Dynein-Driven Bidirectional Nuclear Movements and Microtubule Growth Control in Ashbya gossypii
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Clustering of Nuclei in Multinucleated Hyphae Is Prevented by Dynein-Driven Bidirectional Nuclear Movements and Microtubule Growth Control in Ashbya gossypii

机译:达尼丁驱动的双向核运动和棉铃虫微管生长控制防止多核菌丝中的核聚集。

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During filamentous fungus development, multinucleated hyphae employ a system for long-range nuclear migration to maintain an equal nuclear density. A decade ago the microtubule motor dynein was shown to play a central role in this process. Previous studies with Ashbya gossypii revealed extensive bidirectional movements and bypassings of nuclei, an autonomous cytoplasmic microtubule (cMT) cytoskeleton emanating from each nucleus, and pulling of nuclei by sliding of cMTs along the cortex. Here, we show that dynein is the sole motor for bidirectional movements and bypassing because these movements are concomitantly decreased in mutants carrying truncations of the dynein heavy-chain DYN1 promoter. The dynactin component Jnm1, the accessory proteins Dyn2 and Ndl1, and the potential dynein cortical anchor Num1 are also involved in the dynamic distribution of nuclei. In their absence, nuclei aggregate to different degrees, whereby the mutants with dense nuclear clusters grow extremely long cMTs. As in budding yeast, we found that dynein is delivered to cMT plus ends, and its activity or processivity is probably controlled by dynactin and Num1. Together with its role in powering nuclear movements, we propose that dynein also plays (directly or indirectly) a role in the control of cMT length. Those combined dynein actions prevent nuclear clustering in A. gossypii and thus reveal a novel cellular role for dynein.
机译:在丝状真菌发育过程中,多核菌丝采用了一种用于长距离核迁移的系统,以维持相等的核密度。十年前,微管马达动力蛋白在这一过程中发挥了核心作用。先前关于棉球菌的研究表明核广泛的双向运动和绕行,从每个核发出的自主性细胞质微管(cMT)细胞骨架,以及通过沿皮层滑动cMT吸引核。在这里,我们表明达因是双向运动和绕过的唯一动力,因为这些运动在带有达因重链 DYN1 启动子截短的突变体中同时减少。动力蛋白成分Jnm1,辅助蛋白Dyn2和Ndl1以及潜在的动力蛋白皮质锚Num1也参与细胞核的动态分布。在它们不存在的情况下,核以不同程度聚集,从而具有密集核簇的突变体生长出非常长的cMT。与发芽酵母一样,我们发现动力蛋白被传递至cMT的末端,其活性或合成能力可能受动力蛋白和Num1的控制。连同其在推动核运动中的作用一起,我们提出了动力蛋白在cMT长度控制中也(直接或间接)起作用。这些联合的动力蛋白作用阻止了棉铃虫中的核簇,从而揭示了动力蛋白的新型细胞作用。

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