CNGC15 and DMI1 ion channel gating in nuclear calcium signaling: opening new questions and closing controversies.

IF 5.6 2区 生物学 Q1 PLANT SCIENCES Journal of Experimental Botany Pub Date : 2024-12-04 DOI:10.1093/jxb/erae352
Catherine N Jacott, Pablo Del Cerro
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Abstract

Nuclear calcium (Ca2+) signaling is crucial for symbiotic interactions between legumes and beneficial microbes, such as rhizobia and arbuscular mycorrhizal fungi. The ion channels DMI1 and CNGC15 are key to generating repetitive nuclear Ca2+ oscillations. Despite more than 20 years of research on symbiotic nuclear Ca2+ spiking, important questions remain, including the exact function of the DMI1 channel. This review highlights recent developments that have filled knowledge gaps regarding the regulation of CNGC15 and its interplay with DMI1. We also explore new insights into the evolutionary conservation of DMI1-induced symbiotic nuclear Ca2+ oscillations and the roles of CNGC15 and DMI1 beyond symbiosis, such as in nitrate signaling, and discuss new questions this raises. As we delve deeper into the regulatory mechanisms and evolutionary history of these ion channels, we move closer to fully understanding the roles of nuclear Ca2+ signaling in plant life.

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核钙通道中的 CNGC15-DMI1 门控:提出新问题,结束争论。
核 Ca²⁺ 信号对于豆科植物与有益微生物(如根瘤菌和丛枝菌根真菌)之间的共生相互作用至关重要。产生重复核 Ca²⁺ 振荡的关键是离子通道 DMI1 和 CNGC15。尽管对共生核 Ca²⁺ 尖峰振荡的研究已超过 20 年,但仍存在一些重要问题,包括 DMI1 通道的确切功能。本综述重点介绍了填补有关 CNGC15 的调控及其与 DMI1 相互作用的知识空白的最新进展。我们还探讨了 DMI1 诱导的共生核 Ca²⁺ 振荡的进化保护以及 CNGC15 和 DMI1 在共生之外的作用(如硝酸盐信号)的新见解,并讨论了由此引发的新问题。随着我们深入研究这些离子通道的调控机制和进化历史,我们将更接近于全面了解核 Ca²⁺ 信号在植物生命中的作用。
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来源期刊
Journal of Experimental Botany
Journal of Experimental Botany 生物-植物科学
CiteScore
12.30
自引率
4.30%
发文量
450
审稿时长
1.9 months
期刊介绍: The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology. Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.
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