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F-BAR蛋白的顺序募集控制酵母芽颈处的细胞骨架串扰。

Sequential recruitment of F-BAR proteins controls cytoskeletal crosstalk at the yeast bud neck.

作者信息

Magliozzi Joseph O, Runyan Lucas A, Dutta Priyanka, Hoeprich Gregory J, Goode Bruce L

机构信息

Department of Biology, Rosenstiel Basic Medical Science Research Center, Brandeis University, 415 South Street, Waltham, MA 02454, USA.

Department of Biology, Rosenstiel Basic Medical Science Research Center, Brandeis University, 415 South Street, Waltham, MA 02454, USA.

出版信息

Curr Biol. 2025 Feb 3;35(3):574-590.e10. doi: 10.1016/j.cub.2024.12.011. Epub 2025 Jan 10.

Abstract

In vivo functions of the septin and actin cytoskeletons are closely intertwined, yet the mechanisms underlying septin-actin crosstalk have remained poorly understood. Here, we show that the yeast-bud-neck-associated Fes/CIP4 homology Bar-amphiphysin-Rvs (F-BAR) protein suppressor of yeast profilin 1 (Syp1)/FCHo uses its intrinsically disordered region (IDR) to directly bind and bundle filamentous actin (F-actin) and to physically link septins and F-actin. Interestingly, the only other F-BAR protein found at the neck during bud development, Hof1, has related activities and also potently inhibits the bud-neck-associated formin Bnr1. However, we find that Syp1 enhances rather than inhibits Bnr1-mediated actin assembly and fully overcomes Hof1-mediated inhibition of Bnr1. Further, during bud development, Syp1 and Hof1 show reciprocal patterns of arrival and departure from the bud neck, and in vitro Syp1 and Hof1 compete for septin binding. Together, our observations suggest that as the bud grows, the relative levels of these two F-BAR proteins at the bud neck invert, driving changes in septin organization, septin-actin linkage, and formin activity. More broadly, our findings expand the functional roles of Syp1/FCHo family proteins and our understanding of the working relationships among F-BAR proteins in cytoskeletal regulation.

摘要

Septin细胞骨架和肌动蛋白细胞骨架的体内功能紧密相连,然而,Septin-肌动蛋白相互作用的潜在机制仍未得到充分理解。在此,我们表明酵母芽颈相关的Fes/CIP4同源性Bar-双栖蛋白-Rvs(F-BAR)蛋白酵母 profilin 1(Syp1)/FCHo的抑制因子利用其内在无序区域(IDR)直接结合并捆绑丝状肌动蛋白(F-肌动蛋白),并在物理上连接Septin和F-肌动蛋白。有趣的是,在芽发育过程中在颈部发现的唯一另一种F-BAR蛋白Hof1具有相关活性,并且还能有效抑制芽颈相关的formin Bnr1。然而,我们发现Syp1增强而非抑制Bnr1介导的肌动蛋白组装,并完全克服Hof1介导的对Bnr1的抑制。此外,在芽发育过程中,Syp1和Hof1在芽颈处呈现出相互的到达和离开模式,并且在体外Syp1和Hof1竞争与Septin结合。总之,我们的观察结果表明,随着芽的生长,这两种F-BAR蛋白在芽颈处的相对水平发生反转,驱动Septin组织、Septin-肌动蛋白连接和formin活性的变化。更广泛地说,我们的发现扩展了Syp1/FCHo家族蛋白的功能作用以及我们对F-BAR蛋白在细胞骨架调节中的工作关系的理解。

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