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破坏苔藓中极化细胞扩张和发育的新型小分子

Novel small molecules disrupting polarized cell expansion and development in the moss, .

作者信息

Singh Prerna, Kadofusa Naoya, Sato Ayato, Naramoto Satoshi, Fujita Tomomichi

机构信息

Graduate School of Life Science, Hokkaido University.

Institute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University.

出版信息

Plant Biotechnol (Tokyo). 2025 Jun 25;42(2):131-143. doi: 10.5511/plantbiotechnology.25.0209a.

Abstract

Tip growth is vital for plant growth and development, yet the regulatory mechanisms governing this process remain incompletely understood. In this study, we identify Reagent F4, a novel small molecule that disrupts tip growth and polarized cell expansion in the moss, protonemata. Through unbiased chemical screening, we found that Reagent F4 induces abnormal protonemal morphology, characterized by reduced cell elongation and stunted cell expansion. Our analyses revealed that F4 treatment triggers actin depolymerization and disrupts apical actin foci, which are critical for initiating and maintaining tip growth. Additionally, both acute and prolonged F4 exposure led to mislocalization of ROP GTPase, a key regulator of cell polarity. Transcriptomic analyses of F4 treated protonemata show significant downregulation of genes involved in lipid asymmetry, a process essential for polarized growth. These findings establish Reagent F4 as a valuable tool to investigate the molecular mechanisms governing tip growth in and highlight the potential role of lipid asymmetry in coordinating cytoskeletal organization and membrane polarity.

摘要

顶端生长对植物的生长和发育至关重要,然而,控制这一过程的调控机制仍未完全明确。在本研究中,我们鉴定出试剂F4,这是一种新型小分子,它会破坏苔藓原丝体中的顶端生长和细胞极性扩展。通过无偏向化学筛选,我们发现试剂F4会诱导原丝体形态异常,其特征是细胞伸长减少和细胞扩展受阻。我们的分析表明,F4处理会引发肌动蛋白解聚并破坏顶端肌动蛋白焦点,而这对启动和维持顶端生长至关重要。此外,急性和长时间暴露于F4都会导致ROP GTPase(细胞极性的关键调节因子)定位错误。对经F4处理的原丝体进行的转录组分析显示,参与脂质不对称性的基因显著下调,而脂质不对称性是极性生长所必需的过程。这些发现确立了试剂F4作为研究顶端生长分子机制的宝贵工具,并突出了脂质不对称性在协调细胞骨架组织和膜极性方面的潜在作用。

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