Muhammad Riaz , Erum Yasmeen , Moyang Liu , Hafiz Saqib Ali , Mengli Lv , Hu Shi , Chuanhui Du , Tiantian Dong , Zhenxin Liu , Qingwei Song , QiJun Ma , Kaijing Zuo
{"title":"通过比较转录组学阐明线粒体氧化磷酸化(mtOXPHOS)是拟南芥在热胁迫下测量波动的哨兵","authors":"Muhammad Riaz , Erum Yasmeen , Moyang Liu , Hafiz Saqib Ali , Mengli Lv , Hu Shi , Chuanhui Du , Tiantian Dong , Zhenxin Liu , Qingwei Song , QiJun Ma , Kaijing Zuo","doi":"10.1016/j.stress.2024.100613","DOIUrl":null,"url":null,"abstract":"<div><div>Heat stress has destructive effects on crop production and quality posing a grave threat to food security worldwide. Recent studies have elucidated the complicated transcriptional regulatory networks involved in heat stress, but how the organelles of plants adapt to heat stress remains largely unknown. To analyze the molecular mechanism of the organelle's contribution to plant heat adaptation, we utilized publicly available transcriptomic datasets to identify the central module and key pathway responding to heat stress in <em>Arabidopsis thaliana</em>. The co-expression network showed that the mitochondrial electron transport chain (mETC) and ATP synthase in the pathway of mitochondrial oxidative phosphorylation (mtOXPHOS) shows the highest correlation and ranks at the top among the characterized pathways. Comparative transcriptomic analysis indicated that the genes of the mtOXPHOS pathway and ATP synthesis exhibited different expression profiles between the roots and leaves under high temperature stress. Suppressed OXPHOS and respiration due to the dysfunction of mitochondria in MRPL1 mutants exhibited thermosensitivity. Extensive genetic reprogramming through ROS, Ca<sup>+2</sup>, and retrograde signaling pathways that mitigate stress was also observed. In addition, NAD<sup>+</sup>/NADH ratio indicated redox balancing in response to high temperature. We further verified that, lower mtOXPHOS also affects photosystem II under heat stress. Hence, we concluded that appropriate mitochondrial dynamics, higher oxygen consumption rate (∼15.49-fold higher than mutant at 44 °C) and the sufficient levels of ATP production in roots (∼1.78-fold higher than mutant at 44 °C) ensure plant survival under heat stress. These findings provide valuable clues about mitochondrial signaling, OXHOPS, and energy status in response to heat stress in planta.</div></div>","PeriodicalId":34736,"journal":{"name":"Plant Stress","volume":"14 ","pages":"Article 100613"},"PeriodicalIF":6.8000,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mitochondrial oxidative phosphorylation (mtOXPHOS) serves as a sentinel to gauge fluctuations under heat stress in Arabidopsis thaliana elucidated by comparative transcriptomics\",\"authors\":\"Muhammad Riaz , Erum Yasmeen , Moyang Liu , Hafiz Saqib Ali , Mengli Lv , Hu Shi , Chuanhui Du , Tiantian Dong , Zhenxin Liu , Qingwei Song , QiJun Ma , Kaijing Zuo\",\"doi\":\"10.1016/j.stress.2024.100613\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Heat stress has destructive effects on crop production and quality posing a grave threat to food security worldwide. Recent studies have elucidated the complicated transcriptional regulatory networks involved in heat stress, but how the organelles of plants adapt to heat stress remains largely unknown. To analyze the molecular mechanism of the organelle's contribution to plant heat adaptation, we utilized publicly available transcriptomic datasets to identify the central module and key pathway responding to heat stress in <em>Arabidopsis thaliana</em>. The co-expression network showed that the mitochondrial electron transport chain (mETC) and ATP synthase in the pathway of mitochondrial oxidative phosphorylation (mtOXPHOS) shows the highest correlation and ranks at the top among the characterized pathways. Comparative transcriptomic analysis indicated that the genes of the mtOXPHOS pathway and ATP synthesis exhibited different expression profiles between the roots and leaves under high temperature stress. Suppressed OXPHOS and respiration due to the dysfunction of mitochondria in MRPL1 mutants exhibited thermosensitivity. Extensive genetic reprogramming through ROS, Ca<sup>+2</sup>, and retrograde signaling pathways that mitigate stress was also observed. In addition, NAD<sup>+</sup>/NADH ratio indicated redox balancing in response to high temperature. We further verified that, lower mtOXPHOS also affects photosystem II under heat stress. Hence, we concluded that appropriate mitochondrial dynamics, higher oxygen consumption rate (∼15.49-fold higher than mutant at 44 °C) and the sufficient levels of ATP production in roots (∼1.78-fold higher than mutant at 44 °C) ensure plant survival under heat stress. These findings provide valuable clues about mitochondrial signaling, OXHOPS, and energy status in response to heat stress in planta.</div></div>\",\"PeriodicalId\":34736,\"journal\":{\"name\":\"Plant Stress\",\"volume\":\"14 \",\"pages\":\"Article 100613\"},\"PeriodicalIF\":6.8000,\"publicationDate\":\"2024-09-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Stress\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2667064X24002665\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Stress","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667064X24002665","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Mitochondrial oxidative phosphorylation (mtOXPHOS) serves as a sentinel to gauge fluctuations under heat stress in Arabidopsis thaliana elucidated by comparative transcriptomics
Heat stress has destructive effects on crop production and quality posing a grave threat to food security worldwide. Recent studies have elucidated the complicated transcriptional regulatory networks involved in heat stress, but how the organelles of plants adapt to heat stress remains largely unknown. To analyze the molecular mechanism of the organelle's contribution to plant heat adaptation, we utilized publicly available transcriptomic datasets to identify the central module and key pathway responding to heat stress in Arabidopsis thaliana. The co-expression network showed that the mitochondrial electron transport chain (mETC) and ATP synthase in the pathway of mitochondrial oxidative phosphorylation (mtOXPHOS) shows the highest correlation and ranks at the top among the characterized pathways. Comparative transcriptomic analysis indicated that the genes of the mtOXPHOS pathway and ATP synthesis exhibited different expression profiles between the roots and leaves under high temperature stress. Suppressed OXPHOS and respiration due to the dysfunction of mitochondria in MRPL1 mutants exhibited thermosensitivity. Extensive genetic reprogramming through ROS, Ca+2, and retrograde signaling pathways that mitigate stress was also observed. In addition, NAD+/NADH ratio indicated redox balancing in response to high temperature. We further verified that, lower mtOXPHOS also affects photosystem II under heat stress. Hence, we concluded that appropriate mitochondrial dynamics, higher oxygen consumption rate (∼15.49-fold higher than mutant at 44 °C) and the sufficient levels of ATP production in roots (∼1.78-fold higher than mutant at 44 °C) ensure plant survival under heat stress. These findings provide valuable clues about mitochondrial signaling, OXHOPS, and energy status in response to heat stress in planta.
期刊介绍:
The journal Plant Stress deals with plant (or other photoautotrophs, such as algae, cyanobacteria and lichens) responses to abiotic and biotic stress factors that can result in limited growth and productivity. Such responses can be analyzed and described at a physiological, biochemical and molecular level. Experimental approaches/technologies aiming to improve growth and productivity with a potential for downstream validation under stress conditions will also be considered. Both fundamental and applied research manuscripts are welcome, provided that clear mechanistic hypotheses are made and descriptive approaches are avoided. In addition, high-quality review articles will also be considered, provided they follow a critical approach and stimulate thought for future research avenues.
Plant Stress welcomes high-quality manuscripts related (but not limited) to interactions between plants and:
Lack of water (drought) and excess (flooding),
Salinity stress,
Elevated temperature and/or low temperature (chilling and freezing),
Hypoxia and/or anoxia,
Mineral nutrient excess and/or deficiency,
Heavy metals and/or metalloids,
Plant priming (chemical, biological, physiological, nanomaterial, biostimulant) approaches for improved stress protection,
Viral, phytoplasma, bacterial and fungal plant-pathogen interactions.
The journal welcomes basic and applied research articles, as well as review articles and short communications. All submitted manuscripts will be subject to a thorough peer-reviewing process.