ZmGDI1 Modulates Stomatal Development and Drought Response via the Rho GTPase Pathway Regulation in Maize.

IF 3.6 2区 生物学 Q1 PLANT SCIENCES
Juanjuan Xu, Xiaotong Dong, Kedong Hui, Yuan Liu, Youzhi Li, Xianwei Fan
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引用次数: 0

Abstract

Guanine nucleotide dissociation inhibitors (GDIs) regulate cell signaling in mammals, but their role in stomatal development in plants remains unknown. This study investigates the role of the maize GDI1 (ZmGDI1) in stomatal formation and drought stress responses. Heterologous expression of ZmGDI1 in Arabidopsis reduced the transcription of key stomatal development genes including SPEECHLESS (SPCH), FAMA, and MUTE, resulting in reduced stomatal density by 13% compared to wild-type plants. Conversely, atgdi1 loss-of-function mutants exhibited increased stomatal density and upregulation of these master regulators, resulting in enhanced drought sensitivity. The phenotypes observed in the atgdi1 mutant were rescued by the expression of ZmGDI1, suggesting that the function of GDIs in stomatal development is conserved across different plant species. ZmGDI1-silenced maize plants generated via virus-induced gene silencing (VIGS) showed a marked increase in stomatal density, confirming the functional conservation of the ZmGDI1 gene. ZmGDI1 was demonstrated to interact with and inhibit the activity of the Rho GTPase ZmROP4, which subsequently associates with ZmPAN1/2 to promote stomatal development. These findings uncover a conserved GDI-ROP signaling module that governs stomatal patterning and provides molecular targets for engineering improved drought tolerance in crops.

ZmGDI1通过Rho GTPase通路调控玉米气孔发育和干旱响应
鸟嘌呤核苷酸解离抑制剂(gdi)在哺乳动物中调节细胞信号传导,但它们在植物气孔发育中的作用尚不清楚。研究了玉米GDI1 (ZmGDI1)在气孔形成和干旱胁迫响应中的作用。ZmGDI1在拟南芥中的异源表达降低了SPCH、FAMA和MUTE等关键气孔发育基因的转录,导致气孔密度比野生型降低13%。相反,atgdi1功能缺失突变体表现出气孔密度增加和这些主要调节因子的上调,导致干旱敏感性增强。在atgdi1突变体中观察到的表型被ZmGDI1的表达所挽救,这表明gdi在气孔发育中的功能在不同植物物种中是保守的。通过病毒诱导基因沉默(VIGS)获得的ZmGDI1沉默玉米植株气孔密度显著增加,证实了ZmGDI1基因的功能保存。ZmGDI1与Rho GTPase ZmROP4相互作用并抑制其活性,ZmROP4随后与ZmPAN1/2结合促进气孔发育。这些发现揭示了一个保守的GDI-ROP信号模块,该模块控制着气孔模式,并为工程提高作物的耐旱性提供了分子靶标。
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来源期刊
Physiologia plantarum
Physiologia plantarum 生物-植物科学
CiteScore
11.00
自引率
3.10%
发文量
224
审稿时长
3.9 months
期刊介绍: Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.
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