Center for Plant Biology, School of Life Sciences, Tsinghua University, Beijing 100084, China.
Key Laboratory of Cell Proliferation and Regulation Biology of Ministry of Education, College of Life Science, Beijing Normal University, Beijing 100875, China.
Curr Biol. 2024 Nov 4;34(21):5040-5053.e6. doi: 10.1016/j.cub.2024.09.053. Epub 2024 Oct 16.
Formin is an important player in promoting apical actin polymerization in pollen tubes, but the mechanism regulating its activity remains unknown. We here identify REN1, a Rho GTPase-activating protein, as a negative regulator of formins in Arabidopsis pollen tubes. Specifically, we found that depletion of REN1 promotes apical actin polymerization and increases the amount of filamentous actin in pollen tubes. Interestingly, the effect of REN1 loss of function phenocopies the effect of formin gain of function, as it causes the formation of supernumerary membrane-derived actin bundles, which leads to tube swelling and membrane deformation. Importantly, inhibition of formins suppresses the phenotypic defects in ren1 mutant pollen tubes. We further demonstrate that REN1 physically interacts with the Arabidopsis formin protein AtFH5, predominantly with the C terminus, and inhibits the ability of AtFH5 to nucleate and assemble actin in vitro. Depletion of AtFH5 partially suppresses the phenotype in ren1 mutant pollen tubes, demonstrating that REN1 regulates apical actin polymerization at least partially through inhibiting AtFH5. We thus uncover a novel mechanism regulating formins and actin polymerization in plants.
formin 是促进花粉管中顶端肌动蛋白聚合的重要参与者,但调节其活性的机制尚不清楚。我们在这里鉴定出 REN1,一种 Rho GTPase 激活蛋白,是拟南芥花粉管中formin 的负调控因子。具体来说,我们发现 REN1 的耗竭促进了顶端肌动蛋白的聚合,并增加了花粉管中丝状肌动蛋白的含量。有趣的是,REN1 功能丧失的效果类似于formin 功能获得的效果,因为它导致了额外的膜衍生肌动蛋白束的形成,从而导致管肿胀和膜变形。重要的是,formin 的抑制抑制了 ren1 突变体花粉管中的表型缺陷。我们进一步证明 REN1 与拟南芥formin 蛋白 AtFH5 物理相互作用,主要与 C 端相互作用,并抑制 AtFH5 在体外起始和组装肌动蛋白的能力。AtFH5 的耗竭部分抑制了 ren1 突变体花粉管中的表型,表明 REN1 通过抑制 AtFH5 来调节顶端肌动蛋白聚合。因此,我们揭示了一种调节植物中formin 和肌动蛋白聚合的新机制。