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Feedback Microtubule Control and Microtubule-Actin Cross-talk in Arabidopsis Revealed by Integrative Proteomic and Cell Biology Analysis of KATANIN 1 Mutants

机译:通过蛋白质组学和KATANIN 1突变体细胞生物学分析揭示拟南芥中的反馈微管控制和微管肌动蛋白的串扰。

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摘要

Microtubule organization and dynamics are critical for key developmental processes such as cell division, elongation, and morphogenesis. Microtubule severing is an essential regulator of microtubules and is exclusively executed by KATANIN 1 in Arabidopsis. In this study, we comparatively studied the proteome-wide effects in two KATANIN 1 mutants. Thus, shotgun proteomic analysis of roots and aerial parts of single nucleotide mutant fra2 and T-DNA insertion mutant ktn1-2 was carried out. We have detected 42 proteins differentially abundant in both fra2 and ktn1-2. KATANIN 1 dysfunction altered the abundance of proteins involved in development, metabolism, and stress responses. The differential regulation of tubulins and microtubule-destabilizing protein MDP25 implied a feedback microtubule control in KATANIN 1 mutants. Furthermore, deregulation of profilin 1, actin-depolymerizing factor 3, and actin 7 was observed. These findings were confirmed by immunoblotting analysis of actin and by microscopic observation of actin filaments using fluorescently labeled phalloidin. Results obtained by quantitative RT-PCR analysis revealed that changed protein abundances were not a consequence of altered expression levels of corresponding genes in the mutants. In conclusion, we show that abundances of several cytoskeletal proteins as well as organization of microtubules and the actin cytoskeleton are amended in accordance with defective microtubule severing.
机译:微管的组织和动力学对于关键的发育过程如细胞分裂,伸长和形态发生至关重要。微管切断是微管的基本调节剂,由拟南芥中的KATANIN 1专门执行。在这项研究中,我们比较研究了两个KATANIN 1突变体对蛋白质组的影响。因此,对单核苷酸突变体fra2和T-DNA插入突变体ktn1-2的根和空中部分进行了shot弹枪蛋白质组学分析。我们已经检测到在fra2和ktn1-2中差异丰富的42种蛋白质。 KATANIN 1功能障碍改变了参与发育,代谢和应激反应的蛋白质的丰度。微管蛋白和微管稳定蛋白MDP25的差异调节意味着在KATANIN 1突变体中反馈微管的控制。此外,观察到脯氨酸蛋白1,肌动蛋白解聚因子3和肌动蛋白7的失调。通过肌动蛋白的免疫印迹分析和使用荧光标记的鬼笔环肽对肌动蛋白丝的显微镜观察,证实了这些发现。通过定量RT-PCR分析获得的结果表明,改变的蛋白质丰度不是突变体中相应基因表达水平改变的结果。总之,我们表明,根据有缺陷的微管切断,可以修正一些细胞骨架蛋白的丰度以及微管和肌动蛋白细胞骨架的组织。

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