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定量氧化还原蛋白质组学揭示了甜菜单体附加系M14根系耐盐性的分子机制。

Quantitative redox proteomics revealed molecular mechanisms of salt tolerance in the roots of sugar beet monomeric addition line M14.

作者信息

Liu He, Du Xiaoxue, Zhang Jialin, Li Jinna, Chen Sixue, Duanmu Huizi, Li Haiying

机构信息

Key Laboratory of Molecular Biology of Heilongjiang Province, College of Life Sciences, Heilongjiang University, Harbin, 150080, China.

Engineering Research Center of Agricultural Microbiology Technology, Ministry of Education, Heilongjiang University, Harbin, 150080, China.

出版信息

Bot Stud. 2022 Mar 5;63(1):5. doi: 10.1186/s40529-022-00337-w.

Abstract

BACKGROUND

Salt stress is often associated with excessive production of reactive oxygen species (ROS). Oxidative stress caused by the accumulation of ROS is a major factor that negatively affects crop growth and yield. Root is the primary organ that senses and transmits the salt stress signal to the whole plant. How oxidative stress affect redox sensitive proteins in the roots is not known.

RESULTS

In this study, the redox proteome of sugar beet M14 roots under salt stress was investigated. Using iTRAQ reporters, we determined that salt stress caused significant changes in the abundance of many proteins (2305 at 20 min salt stress and 2663 at 10 min salt stress). Using iodoTMT reporters, a total of 95 redox proteins were determined to be responsive to salt stress after normalizing again total protein level changes. Notably, most of the differential redox proteins were involved in metabolism, ROS homeostasis, and stress and defense, while a small number play a role in transport, biosynthesis, signal transduction, transcription and photosynthesis. Transcription levels of 14 genes encoding the identified redox proteins were analyzed using qRT-PCR. All the genes were induced by salt stress at the transcriptional level.

CONCLUSIONS

Based on the redox proteomics results, we construct a map of the regulatory network of M14 root redox proteins in response to salt stress. This study further refines the molecular mechanism of salt resistance at the level of protein redox regulation.

摘要

背景

盐胁迫通常与活性氧(ROS)的过量产生有关。由ROS积累引起的氧化应激是对作物生长和产量产生负面影响的主要因素。根是感知并将盐胁迫信号传递到整个植株的主要器官。氧化应激如何影响根中对氧化还原敏感的蛋白质尚不清楚。

结果

在本研究中,对盐胁迫下甜菜M14根的氧化还原蛋白质组进行了研究。使用iTRAQ试剂,我们确定盐胁迫导致许多蛋白质丰度发生显著变化(盐胁迫20分钟时有2305种,盐胁迫10分钟时有2663种)。使用碘代TMT试剂,在再次标准化总蛋白质水平变化后,共确定95种氧化还原蛋白质对盐胁迫有响应。值得注意的是,大多数差异氧化还原蛋白质参与代谢、ROS稳态以及应激和防御,而少数在运输、生物合成、信号转导、转录和光合作用中发挥作用。使用qRT-PCR分析了14个编码已鉴定氧化还原蛋白质的基因的转录水平。所有基因在转录水平上均受盐胁迫诱导。

结论

基于氧化还原蛋白质组学结果,我们构建了M14根氧化还原蛋白质响应盐胁迫的调控网络图。本研究进一步在蛋白质氧化还原调控水平上完善了耐盐分子机制。

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