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来自不同途径的氧化脂质通过呼吸复合体III触发线粒体应激信号。

Oxylipins From Different Pathways Trigger Mitochondrial Stress Signaling Through Respiratory Complex III.

作者信息

Izquierdo Yovanny, Muñiz Luis, Vicente Jorge, Kulasekaran Satish, Aguilera Verónica, López Sánchez Ana, Martínez-Ayala Ada, López Bran, Cascón Tomás, Castresana Carmen

机构信息

Department of Plant Molecular Genetics, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.

School of Biosciences, University of Nottingham, Nottingham, United Kingdom.

出版信息

Front Plant Sci. 2021 Jul 29;12:705373. doi: 10.3389/fpls.2021.705373. eCollection 2021.

DOI:10.3389/fpls.2021.705373
PMID:34394161
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8358658/
Abstract

Plant oxylipins are signaling molecules produced from fatty acids by oxidative pathways, mainly initiated by 9- and 13-lipoxygenases (9-LOX and 13-LOX), alpha-dioxygenases or non-enzymatic oxidation. Oxylipins from the 9-LOX pathway induce oxidative stress and control root development and plant defense. These activities have been associated with mitochondrial processes, but precise cellular targets and pathways remain unknown. In order to study oxylipin signaling, we previously generated a collection of mutants that were insensitive to the 9-LOX products 9()-hydroxy-10,12, 15-octadecatrienoic acid (9-HOT) and its ketone derivative 9-KOT ( mutants). Here, we describe , and mutants, all affected in nucleus-encoded mitochondrial proteins, and use them to study the role of mitochondria in oxylipin signaling. Functional and phenotypic analyses showed that plants displayed mitochondrial aggregation, reduced respiration rates and resistance to the complex III inhibitor Antimycin A (AA), thus indicating a close similarity of the oxylipin signaling and mitochondrial stress. Application of 9-HOT and 9-KOT protected plants against subsequent mitochondrial stress, whereas they boosted root growth reduction when applied in combination with complex III inhibitors but did not with inhibitors of other respiratory complexes. A similar effect was caused by linear-chain oxylipins from 13-LOX or non-enzymatic pathways having α,β-unsaturated hydroxyl or keto groups in their structure. Studies to investigate 9-HOT and 9-KOT activity indicated that they do not reduce respiration rates, but their action is primarily associated with enhanced ROS responses. This was supported by the results showing that 9-HOT or 9-KOT combined with AA amplified the expression of oxylipin- and ROS-responding genes but not of the AA marker , thus implying the activation of a specific mitochondria retrograde signaling pathway. Our results implicate mitochondrial complex III as a hub in the signaling activity of multiple oxylipin pathways and point at downstream ROS responses as components of oxylipin function.

摘要

植物氧脂素是通过氧化途径由脂肪酸产生的信号分子,主要由9-脂氧合酶和13-脂氧合酶(9-LOX和13-LOX)、α-双加氧酶或非酶氧化引发。来自9-LOX途径的氧脂素诱导氧化应激并控制根系发育和植物防御。这些活性与线粒体过程有关,但精确的细胞靶点和途径仍不清楚。为了研究氧脂素信号传导,我们之前构建了一系列对9-LOX产物9()-羟基-10,12,15-十八碳三烯酸(9-HOT)及其酮衍生物9-KOT不敏感的突变体(突变体)。在这里,我们描述了、和突变体,它们都在核编码的线粒体蛋白中受到影响,并利用它们来研究线粒体在氧脂素信号传导中的作用。功能和表型分析表明,植物表现出线粒体聚集、呼吸速率降低以及对复合物III抑制剂抗霉素A(AA)的抗性,因此表明氧脂素信号传导与线粒体应激密切相似。施用9-HOT和9-KOT可保护植物免受随后的线粒体应激,而当它们与复合物III抑制剂联合施用时会加剧根系生长减少,但与其他呼吸复合物抑制剂联合施用时则不会。结构中具有α,β-不饱和羟基或酮基的来自13-LOX或非酶途径的线性链氧脂素也会产生类似的效果。研究9-HOT和9-KOT活性表明它们不会降低呼吸速率,但其作用主要与增强的ROS反应相关。这得到了以下结果的支持:9-HOT或9-KOT与AA联合可放大氧脂素和ROS反应基因的表达,但不会放大AA标记物的表达,因此暗示激活了特定的线粒体逆行信号通路。我们的结果表明线粒体复合物III是多种氧脂素途径信号传导活性的枢纽,并指出下游ROS反应是氧脂素功能的组成部分。

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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7438/8358658/07b17e492e14/fpls-12-705373-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7438/8358658/a8ddf748bd2f/fpls-12-705373-g0008.jpg
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