Revealing the complexity of protein abundance in chickpea root under drought-stress using a comparative proteomics approach

被引:23
|
作者
Gupta, Swati [1 ,2 ]
Mishra, Shashank Kumar [1 ]
Misra, Sankalp [1 ,2 ]
Pandey, Vivek [3 ]
Agrawal, Lalit [1 ,4 ]
Nautiyal, Chandra Shekhar [1 ]
Chauhan, Puneet Singh [1 ]
机构
[1] Council Sci & Ind Res Natl Bot Res Inst CSIR NBRI, Microbial Technol Div, Rana Pratap Marg, Lucknow 226001, Uttar Pradesh, India
[2] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
[3] Council Sci & Ind Res Natl Bot Res Inst CSIR NBRI, Plant Ecol & Environm Sci, Rana Pratap Marg, Lucknow 226001, Uttar Pradesh, India
[4] Doon Business Sch, Dept Agr & Allied Sci, Dehra Dun 248001, Uttarakhand, India
关键词
Drought; Proteomics; Chickpea root; 2-DE; MALDI-MS/MS; Western blotting; PLASMA-MEMBRANE; RESPONSES; ARABIDOPSIS; TOLERANCE; VARIETIES; CHAPERONE; PLANTS; HEAT; GENE; SALT;
D O I
10.1016/j.plaphy.2020.03.005
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Global warming has reached an alarming situation, which led to a dangerous climatic condition. The irregular rainfalls and land degradation are the significant consequences of these climatic changes causing a decrease in crop productivity. The effect of drought and its tolerance mechanism, a comparative roots proteomic analysis of chickpea seedlings grown under hydroponic conditions for three weeks, performed at different time points using 2-Dimensional gel electrophoresis (2-DE). After PD-Quest analysis, 110 differentially expressed spots subjected to MALDI-TOF/TOF and 75 spots identified with a significant score. These identified proteins classified into eight categories based on their functional annotation. Proteins involved in carbon and energy metabolism comprised 23% of total identified proteins include mainly glyceraldehyde-3-phosphate dehydrogenase, malate dehydrogenase, transaldolase, and isocitrate dehydrogenase. Proteins related to stress response (heat-shock protein, CS domain protein, and chitinase 2-like) contributed 16% of total protein spots followed by 13% involved in protein metabolism (adenosine kinase 2, and protein disulfide isomerase). ROS metabolism contributed 13% (glutathione S-transferase, ascorbate peroxidase, and thioredoxin), and 9% for signal transduction (actin-101, and 14 3 3 like protein B). Five percent protein identified for secondary metabolism (cinnamoyl-CoA reductase1 and chalcone-flavononeisomerase 2) and 7% for nitrogen (N) and amino acid metabolism (glutamine synthetase and homocysteine methyltransferase). The abundance of some proteins validated by using Western blotting and Real-Time-PCR. The detailed information for drought-responsive root protein(s) through comparative proteomics analysis can be utilized in the future for genetic improvement programs to develop droughttolerant chickpea lines.
引用
收藏
页码:88 / 102
页数:15
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