Suppr超能文献

KASH蛋白SINE1和SINE2在保卫细胞肌动蛋白重组、钙振荡和液泡重塑中的不同作用。

Distinct Roles for KASH Proteins SINE1 and SINE2 in Guard Cell Actin Reorganization, Calcium Oscillations, and Vacuolar Remodeling.

作者信息

Biel Alecia, Moser Morgan, Groves Norman R, Meier Iris

机构信息

Department of Molecular Genetics, The Ohio State University, Columbus, OH, United States.

Center for Applied Plant Sciences, The Ohio State University, Columbus, OH, United States.

出版信息

Front Plant Sci. 2022 May 6;13:784342. doi: 10.3389/fpls.2022.784342. eCollection 2022.

Abstract

The linker of nucleoskeleton and cytoskeleton (LINC) complex is a protein complex spanning the inner and outer membranes of the nuclear envelope. Outer nuclear membrane KASH proteins interact in the nuclear envelope lumen with inner nuclear membrane SUN proteins. The paralogous Arabidopsis KASH proteins SINE1 and SINE2 function during stomatal dynamics induced by light-dark transitions and ABA. Previous studies have shown F-actin organization, cytoplasmic calcium (Ca) oscillations, and vacuolar morphology changes are involved in ABA-induced stomatal closure. Here, we show that SINE1 and SINE2 are both required for actin pattern changes during ABA-induced stomatal closure, but influence different, temporally distinguishable steps. External Ca partially overrides the mutant defects. ABA-induced cytoplasmic Ca oscillations are diminished in but not , and this defect can be rescued by both exogenous Ca and F-actin depolymerization. We show first evidence for nuclear Ca oscillations during ABA-induced stomatal closure, which are disrupted in . Vacuolar fragmentation is impaired in both mutants and is partially rescued by F-actin depolymerization. Together, these data indicate distinct roles for SINE1 and SINE2 upstream of this network of players involved in ABA-based stomatal closure, suggesting a role for the nuclear surface in guard cell ABA signaling.

摘要

核骨架与细胞骨架连接复合体(LINC复合体)是一种跨越核膜内膜和外膜的蛋白质复合体。外核膜KASH蛋白在核膜腔中与内核膜SUN蛋白相互作用。拟南芥同源KASH蛋白SINE1和SINE2在光暗转换和脱落酸(ABA)诱导的气孔动态变化过程中发挥作用。先前的研究表明,丝状肌动蛋白(F-肌动蛋白)组织、细胞质钙(Ca)振荡和液泡形态变化参与了ABA诱导的气孔关闭。在此,我们表明,SINE1和SINE2在ABA诱导的气孔关闭过程中肌动蛋白模式变化中都是必需的,但影响不同的、时间上可区分的步骤。外部钙部分克服了突变体缺陷。ABA诱导的细胞质Ca振荡在 中减弱,但在 中未减弱,并且这种缺陷可以通过外源钙和F-肌动蛋白解聚来挽救。我们首次证明了ABA诱导的气孔关闭过程中存在核Ca振荡,而这在 中被破坏。两个突变体中的液泡碎片化均受损,并且通过F-肌动蛋白解聚可部分挽救。总之,这些数据表明SINE1和SINE2在这个基于ABA的气孔关闭相关作用因子网络的上游具有不同作用,提示核表面在保卫细胞ABA信号传导中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc16/9120628/4e9b1965accb/fpls-13-784342-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验