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利用无标记定量蛋白质组学分析鉴定和表征苗期野生稻中与冷胁迫相关的蛋白质。

Identification and characterisation of cold stress-related proteins in Oryza rufipogon at the seedling stage using label-free quantitative proteomic analysis.

机构信息

College of Life Science, Jiangxi Normal University, Nanchang 330022, PR China.

College of Life Science, Jiangxi Normal University, Nanchang 330022, PR China; and Corresponding authors. Email:

出版信息

Funct Plant Biol. 2021 Apr;48(5):542-555. doi: 10.1071/FP20046.

Abstract

In this study, label-free quantitative proteomics were used to study cold stress-related proteins in Dongxiang wild rice (Oryza rufipogon Griff., DWR) and cold sensitive cultivated rice 'Xieqingzao B'(Oryza sativa L. ssp. indica cv., XB). The results demonstrated the presence of 101 and 216 differentially expressed proteins (DEPs) were detected in DWR and XB, respectively, after cold stress. Bioinformatics analysis showed that DWR and XB differed significantly in their ability to scavenge reactive oxygen species (ROS) and regulate energy metabolism. Of the 101 DEPs of DWR, 46 DEPs related to differential expressed genes were also detected by transcriptome analysis. And 13 out of 101 DEPs were located in previous cold related quantitative trait loci (QTL). Quantitative real-time PCR analysis indicated that protein expression and transcription patterns were not similar in XB and DWR. Protein-protein interaction (PPI) network was constituted using the DEPs of DWR and XB, and the following three centre proteins were identified: Q8H3I3, Q9LDN2, and Q2QXR8. Next, we selected a centre protein and two of the 37 DEPs with high levels of differential expression (fold change ≥ 2) were used for cloning and prokaryotic expression. We found that Q5Z9Q8 could significantly improve the cold tolerance of Escherichia coli.

摘要

在这项研究中,我们使用无标记定量蛋白质组学来研究东乡野生稻(Oryza rufipogon Griff.,DWR)和冷敏感栽培稻‘协青早 B’(Oryza sativa L. ssp. indica cv.,XB)中与冷胁迫相关的蛋白质。结果表明,冷胁迫后 DWR 和 XB 分别检测到 101 和 216 个差异表达蛋白(DEPs)。生物信息学分析表明,DWR 和 XB 在清除活性氧(ROS)和调节能量代谢方面的能力存在显著差异。在 DWR 的 101 个 DEPs 中,通过转录组分析还检测到 46 个与差异表达基因相关的 DEPs。101 个 DEPs 中有 13 个位于先前的冷相关数量性状位点(QTL)。实时定量 PCR 分析表明,XB 和 DWR 中的蛋白质表达和转录模式并不相似。使用 DWR 和 XB 的 DEPs 构建蛋白质-蛋白质相互作用(PPI)网络,鉴定出以下三个中心蛋白:Q8H3I3、Q9LDN2 和 Q2QXR8。接下来,我们选择一个中心蛋白和两个差异表达水平较高(倍数变化≥2)的 37 个 DEPs 进行克隆和原核表达。我们发现 Q5Z9Q8 可以显著提高大肠杆菌的耐冷性。

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