Alexander O. Nedo, Huining Liang, Jaya Sriram, Md Abdur Razzak, Jung-Youn Lee, Chandra Kambhamettu, Savithramma P. Dinesh-Kumar, Jeffrey L. Caplan
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引用次数: 0
摘要
叶绿体异常定位 1(CHUP1)在叶绿体间质细胞的叶绿体回避和积累反应中发挥着重要作用。在表皮细胞中,先前的研究表明,沉默 CHUP1 会诱导叶绿体基质和扩大效应触发免疫(ETI);然而,其基本机制在很大程度上仍然未知。CHUP1 具有双重功能,既能锚定叶绿体,又能招募叶绿体相关肌动蛋白(cp-actin)丝,以实现蓝光诱导的运动。为了确定哪种功能对 ETI 至关重要,我们开发了一种方法来量化表皮细胞中叶绿体的锚定和移动。沉默 NbCHUP1 会自动激活表皮叶绿体防御(ECD)反应,包括基质形成、核周叶绿体聚集、表皮叶绿体反应(ECR)和叶绿体活性氧(ROS)--过氧化氢(H2O2)。这些发现表明叶绿体锚定限制了多方面的 ECD 反应。我们的研究结果还表明,在 NbCHUP1 被沉默的植株中,叶绿体 H2O2 的积累并不是表皮叶绿体基部运动增加所必需的,但却是基质增加和 ETI 增强所必需的。这一发现表明,叶绿体去锚化和 H2O2 在 ETI 期间分别发挥着重要作用。
CHUP1 restricts chloroplast movement and effector-triggered immunity in epidermal cells
Chloroplast Unusual Positioning 1 (CHUP1) plays an important role in the chloroplast avoidance and accumulation responses in mesophyll cells. In epidermal cells, prior research showed silencing CHUP1-induced chloroplast stromules and amplified effector-triggered immunity (ETI); however, the underlying mechanisms remain largely unknown.
CHUP1 has a dual function in anchoring chloroplasts and recruiting chloroplast-associated actin (cp-actin) filaments for blue light-induced movement. To determine which function is critical for ETI, we developed an approach to quantify chloroplast anchoring and movement in epidermal cells. Our data show that silencing NbCHUP1 in Nicotiana benthamiana plants increased epidermal chloroplast de-anchoring and basal movement but did not fully disrupt blue light-induced chloroplast movement.
Silencing NbCHUP1 auto-activated epidermal chloroplast defense (ECD) responses including stromule formation, perinuclear chloroplast clustering, the epidermal chloroplast response (ECR), and the chloroplast reactive oxygen species (ROS), hydrogen peroxide (H2O2). These findings show chloroplast anchoring restricts a multifaceted ECD response.
Our results also show that the accumulated chloroplastic H2O2 in NbCHUP1-silenced plants was not required for the increased basal epidermal chloroplast movement but was essential for increased stromules and enhanced ETI. This finding indicates that chloroplast de-anchoring and H2O2 play separate but essential roles during ETI.
期刊介绍:
New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.