Neurodevelopmental disorder-associated CYFIP2 regulates membraneless organelles and eIF2α phosphorylation via protein interactors and actin cytoskeleton.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-09-19 DOI:10.1093/hmg/ddae107
Yinhua Zhang, Hyae Rim Kang, Yukyung Jun, Hyojin Kang, Geul Bang, Ruiying Ma, Sungjin Ju, Da Eun Yoon, Yoonhee Kim, Kyoungmi Kim, Jin Young Kim, Kihoon Han
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Abstract

De novo variants in the Cytoplasmic FMR1-interacting protein 2 (CYFIP2) have been repeatedly associated with neurodevelopmental disorders and epilepsy, underscoring its critical role in brain development and function. While CYFIP2's role in regulating actin polymerization as part of the WAVE regulatory complex (WRC) is well-established, its additional molecular functions remain relatively unexplored. In this study, we performed unbiased quantitative proteomic analysis, revealing 278 differentially expressed proteins (DEPs) in the forebrain of Cyfip2 knock-out embryonic mice compared to wild-type mice. Unexpectedly, these DEPs, in conjunction with previously identified CYFIP2 brain interactors, included not only other WRC components but also numerous proteins associated with membraneless organelles (MLOs) involved in mRNA processing and translation within cells, including the nucleolus, stress granules, and processing bodies. Additionally, single-cell transcriptomic analysis of the Cyfip2 knock-out forebrain revealed gene expression changes linked to cellular stress responses and MLOs. We also observed morphological changes in MLOs in Cyfip2 knock-out brains and CYFIP2 knock-down cells under basal and stress conditions. Lastly, we demonstrated that CYFIP2 knock-down in cells, potentially through WRC-dependent actin regulation, suppressed the phosphorylation levels of the alpha subunit of eukaryotic translation initiation factor 2 (eIF2α), thereby enhancing protein synthesis. These results suggest a physical and functional connection between CYFIP2 and various MLO proteins and also extend CYFIP2's role within the WRC from actin regulation to influencing eIF2α phosphorylation and protein synthesis. With these dual functions, CYFIP2 may fine-tune the balance between MLO formation/dynamics and protein synthesis, a crucial aspect of proper mRNA processing and translation.

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神经发育障碍相关的CYFIP2通过蛋白相互作用体和肌动蛋白细胞骨架调节无膜细胞器和eIF2α磷酸化。
细胞质 FMR1 相互作用蛋白 2(CYFIP2)的新变异屡次与神经发育障碍和癫痫有关,突显了它在大脑发育和功能中的关键作用。虽然 CYFIP2 作为 WAVE 调控复合物(WRC)的一部分在调节肌动蛋白聚合中的作用已得到证实,但其其他分子功能相对来说仍未得到探索。在这项研究中,我们进行了无偏见的定量蛋白质组分析,发现与野生型小鼠相比,Cyfip2 基因敲除胚胎小鼠前脑中有 278 个差异表达蛋白(DEPs)。出乎意料的是,这些DEPs与之前发现的CYFIP2脑相互作用蛋白结合在一起,不仅包括其他WRC成分,还包括与细胞内mRNA加工和翻译过程中涉及的无膜细胞器(MLO)相关的大量蛋白,包括核仁、应激颗粒和加工体。此外,对 Cyfip2 基因敲除前脑的单细胞转录组分析显示,基因表达的变化与细胞应激反应和 MLO 有关。我们还观察到了Cyfip2基因敲除大脑和CYFIP2基因敲除细胞在基础和应激条件下MLO的形态变化。最后,我们证实,CYFIP2敲除细胞可能通过依赖于 WRC 的肌动蛋白调控,抑制了真核翻译起始因子 2(eIF2α)α 亚基的磷酸化水平,从而促进了蛋白质的合成。这些结果表明,CYFIP2 与各种 MLO 蛋白之间存在着物理和功能上的联系,同时也将 CYFIP2 在 WRC 中的作用从肌动蛋白调控扩展到影响 eIF2α 磷酸化和蛋白质合成。通过这些双重功能,CYFIP2 可微调 MLO 形成/动力学与蛋白质合成之间的平衡,这是正确处理 mRNA 和翻译的一个重要方面。
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