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An ancient Sec10–formin fusion provides insights into actin-mediated regulation of exocytosis

机译:古老的Sec10-formin融合蛋白提供了肌动蛋白介导的胞吐作用调节的见解

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摘要

Exocytosis, facilitated by the exocyst, is fundamentally important for remodeling cell walls and membranes. Here, we analyzed For1F, a novel gene that encodes a fusion of an exocyst subunit (Sec10) and an actin nucleation factor (formin). We showed that the fusion occurred early in moss evolution and has been retained for more than 170 million years. In Physcomitrella patens, For1F is essential, and the expressed protein is a fusion of Sec10 and formin. Reduction of For1F or actin filaments inhibits exocytosis, and For1F dynamically associates with Sec6, another exocyst subunit, in an actin-dependent manner. Complementation experiments demonstrate that constitutive expression of either half of the gene or the paralogous Sec10b rescues loss of For1F, suggesting that fusion of the two domains is not essential, consistent with findings in yeast, where formin and the exocyst are linked noncovalently. Although not essential, the fusion may have had selective advantages and provides a unique opportunity to probe actin regulation of exocytosis.
机译:由胞囊促进的胞吐作用对于重塑细胞壁和膜至关重要。在这里,我们分析了For1F,这是一种编码外囊亚基(Sec10)与肌动蛋白成核因子(formin)融合的新型基因。我们证明了聚变发生在苔藓进化的早期,并且已经保留了超过1.7亿年。在小立碗藓中,For1F是必不可少的,表达的蛋白质是Sec10和FORMIN的融合体。 For1F或肌动蛋白丝的减少会抑制胞吐作用,并且For1F以肌动蛋白依赖性的方式与另一个胞囊亚基Sec6动态缔合。互补实验表明,该基因的一半或旁系Sec10b的组成型表达可挽救For1F的丢失,这表明这两个域的融合不是必需的,这与酵母中的发现相符,因为其中的甲醛和外囊是非共价连接的。尽管不是必需的,但融合可能具有选择优势,并提供了探索肌动蛋白调节胞吐作用的独特机会。

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