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Research progress on the physiological,biochemical and molecular regulatory mechanisms of fruit tree responses to high-temperature stress
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作者 que wang Yaqiong Wu +2 位作者 Wenlong Wu Lianfei Lyu Weilin Li 《Horticultural Plant Journal》 2025年第1期1-14,共14页
Fruit trees face various adverse environmental factors,such as extreme hydrothermal changes,soil salinization and low precipitation,leading to different types of stress.High temperature is one of the main factors affe... Fruit trees face various adverse environmental factors,such as extreme hydrothermal changes,soil salinization and low precipitation,leading to different types of stress.High temperature is one of the main factors affecting the growth of fruit trees,and an appropriate ambient temperature is a necessary condition for the normal growth and development of fruit trees.Since the 20th century,due to the intensification of the greenhouse effect and global warming,there has been a significant increase in the occurrence and duration of extreme hot weather in summer has been occurring frequently and for longer durations.Thus,the growth and production of fruit trees are affected by severe hightemperature stress.Therefore,this paper primarily summarized the impacts of high-temperature stress on fruit growth and development,flowering,fruiting,fruit setting and quality.It also discussed the physiological and biochemical responses of fruit trees to high-temperature stress,research progress on the molecular mechanisms and signal transduction pathways underlying fruit tree resistance to heat or high temperature,and research on the investigation of relevant metabolites of fruit trees under stress conditions.The future research directions were discussed,and prospects and potential difficulties were proposed to serve a reference for further investigation on the high-temperature tolerance of fruit trees. 展开更多
关键词 Heat shock Heat resistance Regulatory mechanisms MIRNA Fruit crop
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DEAD-box helicase 17(DDX17)protects cardiac function by promoting mitochondrial homeostasis in heart failure 被引量:8
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作者 Mingjing Yan Junpeng Gao +24 位作者 Ming Lan que wang Yuan Cao Yuxuan Zheng Yao Yang Wenlin Li Xiaoxue Yu Xiuqing Huang Lin Dou Bing Liu Junmeng Liu Hongqiang Cheng Kunfu Ouyang Kun Xu Shenghui Sun Jin Liu Weiqing Tang Xiyue Zhang Yong Man Liang Sun Jianping Cai Qing He Fuchou Tang Jian Li Tao Shen 《Signal Transduction and Targeted Therapy》 SCIE CSCD 2024年第6期2774-2790,共17页
DEAD-box helicase 17(DDX17)is a typical member of the DEAD-box family with transcriptional cofactor activity.Although DDX17 is abundantly expressed in the myocardium,its role in heart is not fully understood.We genera... DEAD-box helicase 17(DDX17)is a typical member of the DEAD-box family with transcriptional cofactor activity.Although DDX17 is abundantly expressed in the myocardium,its role in heart is not fully understood.We generated cardiomyocyte-specific Ddx17-knockout mice(Ddx17-cKO),cardiomyocyte-specific Ddx17 transgenic mice(Ddx17-Tg),and various models of cardiomyocyte injury and heart failure(HF).DDX17 is downregulated in the myocardium of mouse models of heart failure and cardiomyocyte injury.Cardiomyocyte-specific knockout of Ddx17 promotes autophagic flux blockage and cardiomyocyte apoptosis,leading to progressive cardiac dysfunction,maladaptive remodeling and progression to heart failure.Restoration of DDX17 expression in cardiomyocytes protects cardiac function under pathological conditions.Further studies showed that DDX17 can bind to the transcriptional repressor B-cell lymphoma 6(BCL6)and inhibit the expression of dynamin-related protein 1(DRP1).When DDX17 expression is reduced,transcriptional repression of BCL6 is attenuated,leading to increased DRP1 expression and mitochondrial fission,which in turn leads to impaired mitochondrial homeostasis and heart failure.We also investigated the correlation of DDX17 expression with cardiac function and DRP1 expression in myocardial biopsy samples from patients with heart failure.These findings suggest that DDX17 protects cardiac function by promoting mitochondrial homeostasis through the BCL6-DRP1 pathway in heart failure. 展开更多
关键词 DDX17 HOMEOSTASIS cardiac
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