University School of Biotechnology, G.G.S. Indraprastha University, Sector 16C, Dwarka, New Delhi, 110078, India.
School of Basic and Applied Sciences, Maharaja Agrasen University, Baddi, Distt. Solan, Himachal Pradesh, 174103, India.
Sci Rep. 2019 Apr 9;9(1):5838. doi: 10.1038/s41598-019-42084-2.
G-protein signaling components have been attributed many biological roles in plants, but the extent of involvement of G-protein coupled receptor 1 (GCR1) with the Gα (GPA1) remained unknown. To address this, we have performed transcriptomic analyses on Arabidopsis gpa1-5gcr1-5 double mutant and identified 656 differentially expressed genes (DEGs). MapMan and Gene Ontology analyses revealed global transcriptional changes associated with external stimulus, cell wall organization/biogenesis and secondary metabolite process among others. Comparative transcriptomic analyses using the single and double mutants of gcr1-5 and gpa1-5 identified 194, 139 and 391 exclusive DEGs respectively, whereas 64 DEGs were common to all three mutants. Further, pair wise comparison of DEGs of double mutant with single mutants of gcr1-5 or gpa1-5 showed about one-third and over half common DEGs, respectively. Further analysis of the DEGs exclusive to the double mutant using protein-protein interaction networks revealed molecular complexes associated with nitrate and light signaling and plant-pathogen interactions among others. Physiological and molecular validation of nitrate-response revealed the sensitivity of germination to low N in the double mutant and differential expression of nitrate transporter (and nitrate reductase in all three mutants). Taken together, GCR1 and GPA1 work in partnership as well as independently to regulate different pathways.
G 蛋白信号成分在植物中具有许多生物学功能,但 G 蛋白偶联受体 1 (GCR1) 与 Gα (GPA1) 的参与程度尚不清楚。为了解决这个问题,我们对拟南芥 gpa1-5gcr1-5 双突变体进行了转录组分析,鉴定出 656 个差异表达基因 (DEGs)。MapMan 和基因本体论分析揭示了与外部刺激、细胞壁组织/生物发生和次生代谢过程等相关的全局转录变化。使用 gcr1-5 和 gpa1-5 的单突变体和双突变体进行比较转录组分析,分别鉴定出 194、139 和 391 个特有 DEGs,而 64 个 DEGs在所有三个突变体中都是共同的。此外,将双突变体与 gcr1-5 或 gpa1-5 的单突变体的 DEGs 进行两两比较,分别显示约三分之一和一半以上的共同 DEGs。进一步对双突变体特有的 DEGs 进行分析,使用蛋白质-蛋白质相互作用网络揭示了与硝酸盐和光信号以及植物-病原体相互作用等相关的分子复合物。硝酸盐反应的生理和分子验证显示,双突变体对低氮的萌发敏感性以及硝酸盐转运体 (和所有三个突变体中的硝酸盐还原酶) 的差异表达。总之,GCR1 和 GPA1 既可以协同工作,也可以独立工作,以调节不同的途径。