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The use of quantitative imaging to investigate regulators of membrane trafficking in Arabidopsis stomatal closure

机译:使用定量成像来调查拟南芥气孔闭合膜贩运常规的调节器

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摘要

Expansion of gene families facilitates robustness and evolvability of biological processes but impedes functional genetic dissection of signalling pathways. To address this, quantitative analysis of single cell responses can help characterize the redundancy within gene families. We developed high-throughput quantitative imaging of stomatal closure, a response of plant guard cells, and performed a reverse genetic screen in a group of Arabidopsis mutants to five stimuli. Focussing on the intersection between guard cell signalling and the endomembrane system, we identified eight clusters based on the mutant stomatal responses. Mutants generally affected in stomatal closure were mostly in genes encoding SNARE and SCAMP membrane regulators. By contrast, mutants in RAB5 GTPase genes played specific roles in stomatal closure to microbial but not drought stress. Together with timed quantitative imaging of endosomes revealing sequential patterns in FLS2 trafficking, our imaging pipeline can resolve non-redundant functions of the RAB5 GTPase gene family. Finally, we provide a valuable image-based tool to dissect guard cell responses and outline a genetic framework of stomatal closure.
机译:基因家族的扩增促进生物过程的鲁棒性和不变性,但阻碍了信号通路的功能遗传解剖。为了解决这一点,对单细胞反应的定量分析可以有助于在基因家族内的冗余。我们开发了气孔闭合的高通量定量成像,植物防护细胞的响应,并在一组拟南芥突变体中进行了反向遗传筛网至五种刺激。专注于保护细胞信号传导与内膜系统的交叉点,我们基于突变气孔反应确定了八簇。在气孔闭合中受到影响的突变体主要是编码圈套和疏水膜调节剂的基因。相比之下,RAB5 GTPA酶基因中的突变体在气孔闭合到微生物但不干旱胁迫中起特定的作用。与透露FLS2贩运中的序贯模式的定时定量成像一起,我们的成像管道可以解决RAB5 GTPase基因家族的非冗余功能。最后,我们提供了一个有价值的基于图像的工具来解剖保护单元响应并概述气孔闭合的遗传框架。

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