Unraveling the MAPK Signaling Network in Stomatal Development

N. Eckardt
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引用次数: 3

Abstract

role in biotic and abiotic responses and embryo and floral organ development. The answer, in large part, may lie with cell-specific differences in the expression and activation of various components of the MAPK network under different sets of circumstances. Lampard et al. devised a cell-specific assay for assessing the activity and regulation of MAPK modules in stomatal development based a panel of dominant-negative and constitutively active MAPKK variants expressed in discrete stomatal lineage cell types through the use of cell-type specific promoters. The approach was designed to allow investigation into cell-specific aspects of MAPK signaling without inducing pleiotropic phenotypes, which likely result from ubiquitous activation of MAPK signaling. The authors identified expanded roles for MKK4 and MKK5 in negative regulation of stomatal development and, unexpectedly, uncovered both positive and negative regulatory roles for MKK7 and MKK9 at different stages of stomatal development. MKK7 and MKK9 were found to function in inhibition of the first two stages of stomatal development and in promotion of guard cell proliferation at the terminal stages of stomatal development (see figure). The authors present a model of MAPK control of stomatal development that integrates developmental and environmental cues to offer a reasonable explanation of experimental results and highlight unknown components. This work provides significant insight into regulation of stomatal development and is also of broader significance to our understanding of MAPK networks. It shows that MAPK networks can be dissected by modulating the expression of individual components in specific cell types, in this case stomatal lineage cell types. This cell-specific approach should prove useful for the study of other complex signal transduction pathways as well.
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揭示气孔发育中的MAPK信号网络
在生物和非生物反应以及胚胎和花器官发育中的作用。在很大程度上,答案可能在于不同环境下MAPK网络各种成分的表达和激活的细胞特异性差异。Lampard等人设计了一种细胞特异性检测方法,用于评估MAPK模块在气孔发育中的活性和调控,该方法基于一组显性阴性和组成型活性的MAPKK变体,通过使用细胞类型特异性启动子在离散的气孔谱系细胞类型中表达。该方法旨在允许研究MAPK信号的细胞特异性方面,而不会诱导多效表型,这可能是由于MAPK信号的普遍激活造成的。作者发现了MKK4和MKK5在气孔发育负调控中的扩展作用,并且意外地发现了MKK7和MKK9在气孔发育不同阶段的正调控和负调控作用。MKK7和MKK9抑制了气孔发育的前两个阶段,促进了气孔发育终末阶段的保护细胞增殖(见图)。作者提出了一个综合了发育和环境因素的MAPK控制气孔发育的模型,为实验结果提供了合理的解释,并突出了未知的成分。这项工作为气孔发育的调控提供了重要的见解,对我们理解MAPK网络也具有更广泛的意义。这表明MAPK网络可以通过调节特定细胞类型(在这种情况下是气孔系细胞类型)中单个组分的表达来解剖。这种细胞特异性的方法应该证明对其他复杂信号转导途径的研究也是有用的。
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