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拟南芥HD-Zip IV转录因子GLABRA2的核定位由输入蛋白α驱动。

Nuclear localization of Arabidopsis HD-Zip IV transcription factor GLABRA2 is driven by importin α.

作者信息

Ahmad Bilal, Lerma-Reyes Ruben, Mukherjee Thiya, Nguyen Hieu V, Weber Audra L, Cummings Emily E, Schulze Waltraud X, Comer Jeffrey R, Schrick Kathrin

机构信息

Division of Biology, Kansas State University, Manhattan, KS 66506, USA.

Donald Danforth Plant Science Center, Olivette, MO 63132, USA.

出版信息

J Exp Bot. 2024 Oct 30;75(20):6441-6461. doi: 10.1093/jxb/erae326.

Abstract

GLABRA2 (GL2), a class IV homeodomain leucine-zipper (HD-Zip IV) transcription factor from Arabidopsis, is a developmental regulator of specialized cell types in the epidermis. GL2 contains a monopartite nuclear localization sequence (NLS) that is conserved in most HD-Zip IV members across the plants. We demonstrate that NLS mutations affect nuclear transport and result in a loss-of-function phenotypes. NLS fusions to enhanced yellow fluorescent protein (EYFP) show that it is sufficient for nuclear localization in roots and trichomes. Despite partial overlap of the NLS with the homeodomain, genetic dissection indicates that nuclear localization and DNA binding are separable functions. Affinity purification of GL2 from plants followed by MS-based proteomics identified importin α (IMPα) isoforms as potential GL2 interactors. NLS structural prediction and molecular docking studies with IMPα-3 revealed major interacting residues. Cytosolic yeast two-hybrid assays and co-immunoprecipitation experiments with recombinant proteins verified NLS-dependent interactions between GL2 and several IMPα isoforms. IMPα triple mutants (impα-1,2,3) exhibit abnormal trichome formation and defects in GL2 nuclear localization in trichomes, consistent with tissue-specific and redundant functions of IMPα isoforms. Taken together, our findings provide mechanistic evidence for IMPα-dependent nuclear localization of GL2 in Arabidopsis, a process that is critical for cell type differentiation of the epidermis.

摘要

GLABRA2(GL2)是拟南芥中的一种IV类同源异型域亮氨酸拉链(HD-Zip IV)转录因子,是表皮中特化细胞类型的发育调节因子。GL2包含一个单部分核定位序列(NLS),该序列在大多数植物中的HD-Zip IV成员中是保守的。我们证明NLS突变会影响核转运并导致功能丧失表型。与增强型黄色荧光蛋白(EYFP)的NLS融合表明它足以在根和毛状体中进行核定位。尽管NLS与同源异型域部分重叠,但遗传分析表明核定位和DNA结合是可分离的功能。从植物中亲和纯化GL2,然后基于质谱的蛋白质组学鉴定出输入蛋白α(IMPα)异构体为潜在的GL2相互作用蛋白。NLS结构预测和与IMPα-3的分子对接研究揭示了主要的相互作用残基。胞质酵母双杂交试验和重组蛋白的共免疫沉淀实验验证了GL2与几种IMPα异构体之间的NLS依赖性相互作用。IMPα三重突变体(impα-1,2,3)表现出异常的毛状体形成和毛状体中GL2核定位的缺陷,这与IMPα异构体的组织特异性和冗余功能一致。综上所述,我们的研究结果为拟南芥中IMPα依赖的GL2核定位提供了机制证据,这一过程对表皮细胞类型分化至关重要。

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