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黑暗胁迫下本氏烟草的蛋白质组学和代谢组学分析

Proteomic and metabolomic analysis of Nicotiana benthamiana under dark stress.

作者信息

Shen Juan-Juan, Chen Qian-Si, Li Ze-Feng, Zheng Qing-Xia, Xu Ya-Long, Zhou Hui-Na, Mao Hong-Yan, Shen Qi, Liu Ping-Ping

机构信息

College of Chemistry, Zhengzhou University, Zhengzhou, China.

Chemistry Research Institution of Henan Academy of Sciences, Zhengzhou, China.

出版信息

FEBS Open Bio. 2022 Jan;12(1):231-249. doi: 10.1002/2211-5463.13331. Epub 2021 Dec 16.

Abstract

Exposure to extended periods of darkness is a common source of abiotic stress that significantly affects plant growth and development. To understand how Nicotiana benthamiana responds to dark stress, the proteomes and metabolomes of leaves treated with darkness were studied. In total, 5763 proteins and 165 primary metabolites were identified following dark treatment. Additionally, the expression of autophagy-related gene (ATG) proteins was transiently upregulated. Weighted gene coexpression network analysis (WGCNA) was utilized to find the protein modules associated with the response to dark stress. A total of four coexpression modules were obtained. The results indicated that heat-shock protein (HSP70), SnRK1-interacting protein 1, 2A phosphatase-associated protein of 46 kDa (Tap46), and glutamate dehydrogenase (GDH) might play crucial roles in N. benthamiana's response to dark stress. Furthermore, a protein-protein interaction (PPI) network was constructed and top-degreed proteins were predicted to identify potential key factors in the response to dark stress. These proteins include isopropylmalate isomerase (IPMI), eukaryotic elongation factor 5A (ELF5A), and ribosomal protein 5A (RPS5A). Finally, metabolic analysis suggested that some amino acids and sugars were involved in the dark-responsive pathways. Thus, these results provide a new avenue for understanding the defensive mechanism against dark stress at the protein and metabolic levels in N. benthamiana.

摘要

长时间暴露在黑暗中是一种常见的非生物胁迫来源,会显著影响植物的生长和发育。为了了解本氏烟草对黑暗胁迫的响应,研究了经黑暗处理的叶片的蛋白质组和代谢组。黑暗处理后,共鉴定出5763种蛋白质和165种初级代谢产物。此外,自噬相关基因(ATG)蛋白的表达短暂上调。利用加权基因共表达网络分析(WGCNA)来寻找与黑暗胁迫响应相关的蛋白质模块。共获得了四个共表达模块。结果表明,热休克蛋白(HSP70)、SnRK1相互作用蛋白1、46 kDa的2A磷酸酶相关蛋白(Tap46)和谷氨酸脱氢酶(GDH)可能在本氏烟草对黑暗胁迫的响应中起关键作用。此外,构建了蛋白质-蛋白质相互作用(PPI)网络,并预测了高连接度蛋白以确定黑暗胁迫响应中的潜在关键因子。这些蛋白包括异丙基苹果酸异构酶(IPMI)、真核生物延伸因子5A(ELF5A)和核糖体蛋白5A(RPS5A)。最后,代谢分析表明一些氨基酸和糖类参与了黑暗响应途径。因此,这些结果为在蛋白质和代谢水平上理解本氏烟草对黑暗胁迫的防御机制提供了一条新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92b9/8727940/e48f6e487333/FEB4-12-231-g001.jpg

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