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磷脂酶Dδ有助于盐胁迫后皮层微管的恢复。

Phospholipase Dδ assists to cortical microtubule recovery after salt stress.

作者信息

Angelini Jindřiška, Vosolsobě Stanislav, Skůpa Petr, Ho Angela Yeuan Yen, Bellinvia Erica, Valentová Olga, Marc Jan

机构信息

Department of Biochemistry and Microbiology, University of Chemistry and Technology Prague, Technická 3, 166 28, Prague 6, Czech Republic.

Department of Experimental Plant Biology, Faculty of Science, Charles University, Viničná 5, 128 44, Prague 2, Czech Republic.

出版信息

Protoplasma. 2018 Jul;255(4):1195-1204. doi: 10.1007/s00709-018-1204-6. Epub 2018 Jan 24.

Abstract

The dynamic microtubule cytoskeleton plays fundamental roles in the growth and development of plants including regulation of their responses to environmental stress. Plants exposed to hyper-osmotic stress commonly acclimate, acquiring tolerance to variable stress levels. The underlying cellular mechanisms are largely unknown. Here, we show, for the first time, by in vivo imaging approach that linear patterns of phospholipase Dδ match the localization of microtubules in various biological systems, validating previously predicted connection between phospholipase Dδ and microtubules. Both the microtubule and linear phospholipase Dδ structures were disintegrated in a few minutes after treatment with oryzalin or salt. Moreover, by using immunofluorescence confocal microscopy of the cells in the root elongation zone of Arabidopsis, we have shown that the cortical microtubules rapidly depolymerized within 30 min of treatment with 150 or 200 mM NaCl. Within 5 h of treatment, the density of microtubule arrays was partially restored. A T-DNA insertional mutant lacking phospholipase Dδ showed poor recovery of microtubule arrays following salt exposition. The restoration of microtubules was significantly retarded as well as the rate of root growth, but roots of overexpressor GFP-PLDδ prepared in our lab, have grown slightly better compared to wild-type plants. Our results indicate that phospholipase Dδ is involved in salt stress tolerance, possibly by direct anchoring and stabilization of de novo emerging microtubules to the plasma membrane, providing novel insight into common molecular mechanism during various stress events.

摘要

动态微管细胞骨架在植物的生长和发育中发挥着重要作用,包括调节植物对环境胁迫的反应。暴露于高渗胁迫下的植物通常会适应环境,获得对不同胁迫水平的耐受性。其潜在的细胞机制在很大程度上尚不清楚。在这里,我们首次通过体内成像方法表明,磷脂酶Dδ的线性模式与各种生物系统中微管的定位相匹配,验证了先前预测的磷脂酶Dδ与微管之间的联系。用oryzalin或盐处理后,微管和线性磷脂酶Dδ结构在几分钟内就会解体。此外,通过对拟南芥根伸长区细胞进行免疫荧光共聚焦显微镜观察显示,用150或200 mM NaCl处理30分钟内,皮层微管迅速解聚。处理5小时内,微管阵列密度部分恢复。缺乏磷脂酶Dδ的T-DNA插入突变体在盐处理后微管阵列恢复较差。微管的恢复以及根的生长速率均显著延迟,但我们实验室制备的过表达绿色荧光蛋白-磷脂酶Dδ的植株的根比野生型植株生长得稍好。我们的结果表明,磷脂酶Dδ可能通过将新生微管直接锚定并稳定在质膜上而参与盐胁迫耐受性,为各种胁迫事件中的共同分子机制提供了新的见解。

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