Ca2+波和乙烯/JA串扰协调拟南芥根系的伤口反应。

IF 6.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xuemin Ma, M Shamim Hasan, Muhammad Shahzad Anjam, Sakil Mahmud, Sabarna Bhattacharyya, Ute C Vothknecht, Badou Mendy, Florian M W Grundler, Peter Marhavý
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引用次数: 0

摘要

伤害在植物中引发了复杂和多方面的反应。其中,钙(Ca2+)波作为强烈刺激的即时和局部反应,如线虫感染或激光消融。在这里,我们研究了激光消融诱导Ca2+波的传播模式,并观察了谷氨酸受体样通道(GLR3.3/GLR3.6)、拉伸激活阴离子通道MSL10和机械敏感的Ca2+渗透通道MCA1/MCA2对这一过程的影响。这些通道可能通过WRKY33-ACS6调控网络参与乙烯相关信号通路。此外,我们的研究结果表明ACC/乙烯信号调节激光消融后Ca2+波的传播。损伤部位的乙烯感知和合成调节了局部茉莉酸反应,该反应在激光消融时显示出组织特异性模式。总的来说,我们的数据为植物对局部损伤反应的分子和细胞过程提供了新的见解,突出了特定离子通道和激素信号通路在拟南芥根系形成这些反应中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ca2+ waves and ethylene/JA crosstalk orchestrate wound responses in Arabidopsis roots.

Wounding triggers complex and multi-faceted responses in plants. Among these, calcium (Ca2+) waves serve as an immediate and localized response to strong stimuli, such as nematode infection or laser ablation. Here, we investigate the propagation patterns of Ca2+ waves induced by laser ablation and observe that glutamate-receptor-like channels (GLR3.3/GLR3.6), the stretch-activated anion channel MSL10, and the mechanosensitive Ca2+-permeable channels MCA1/MCA2 influence this process. These channels contribute to ethylene-associated signaling pathways, potentially through the WRKY33-ACS6 regulatory network. Furthermore, our findings show that ACC/ethylene signaling modulates Ca2+ wave propagation following laser ablation. Ethylene perception and synthesis at the site of damage regulate the local jasmonate response, which displays tissue-specific patterns upon laser ablation. Overall, our data provide new insights into the molecular and cellular processes underlying plant responses to localized damage, highlighting the roles of specific ion channels and hormone signaling pathways in shaping these responses in Arabidopsis roots.

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来源期刊
EMBO Reports
EMBO Reports 生物-生化与分子生物学
CiteScore
11.20
自引率
1.30%
发文量
267
审稿时长
1 months
期刊介绍: EMBO Reports is a scientific journal that specializes in publishing research articles in the fields of molecular biology, cell biology, and developmental biology. The journal is known for its commitment to publishing high-quality, impactful research that provides novel physiological and functional insights. These insights are expected to be supported by robust evidence, with independent lines of inquiry validating the findings. The journal's scope includes both long and short-format papers, catering to different types of research contributions. It values studies that: Communicate major findings: Articles that report significant discoveries or advancements in the understanding of biological processes at the molecular, cellular, and developmental levels. Confirm important findings: Research that validates or supports existing knowledge in the field, reinforcing the reliability of previous studies. Refute prominent claims: Studies that challenge or disprove widely accepted ideas or hypotheses in the biosciences, contributing to the correction and evolution of scientific understanding. Present null data: Papers that report negative results or findings that do not support a particular hypothesis, which are crucial for the scientific process as they help to refine or redirect research efforts. EMBO Reports is dedicated to maintaining high standards of scientific rigor and integrity, ensuring that the research it publishes contributes meaningfully to the advancement of knowledge in the life sciences. By covering a broad spectrum of topics and encouraging the publication of both positive and negative results, the journal plays a vital role in promoting a comprehensive and balanced view of scientific inquiry. 
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