荧光标签和活性状态对 ROP GTPases 膜定位的影响。

Plant signaling & behavior Pub Date : 2024-12-31 Epub Date: 2024-01-25 DOI:10.1080/15592324.2024.2306790
Jingtong Ruan, Zihan Yin, Peishan Yi
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引用次数: 0

摘要

植物特异性 Rho- 型 GTP 酶(ROPs)是细胞极性和发育的主要调控因子。在过去的 30 年中,人们主要使用融合在氨基末端的荧光蛋白来研究它们的定位和动态,而没有研究它们对蛋白质功能的影响。青苔 Physcomitrium patens 基因组编码四个 rop 基因。在本研究中,我们通过同源重组在野生型和 rop1,2,3 三重突变体的 ROP4 内源氨基末端引入了荧光标签,结果表明荧光标签严重损害了 ROP4 的功能,抑制了其在质膜上的定位。这种表型在缺乏 ROP 相关 GTPase 激活蛋白的突变体中更为严重。通过比较无功能和有功能 ROP4 融合报告物的定位,我们深入了解了 ROPs 与膜结合的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of fluorescent tags and activity status on the membrane localization of ROP GTPases.

Plant-specific Rho-type GTPases (ROPs) are master regulators of cell polarity and development. Over the past 30 years, their localization and dynamics have been largely examined with fluorescent proteins fused at the amino terminus without investigating their impact on protein function. The moss Physcomitrium patens genome encodes four rop genes. In this study, we introduce a fluorescent tag at the endogenous amino terminus of ROP4 in wild-type and rop1,2,3 triple mutant via homologous recombination and demonstrate that the fluorescent tag severely impairs ROP4 function and inhibits its localization on the plasma membrane. This phenotype is exacerbated in mutants lacking ROP-related GTPase-activating proteins. By comparing the localization of nonfunctional and functional ROP4 fusion reporters, we provide insight into the mechanism that governs the membrane association of ROPs.

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