Sultana Nigarin, Islam Shahidul, Juhasz Angela, Yang Rongchang, She Maoyun, Alhabbar Zaid, Zhang Jingjuan, Ma Wujun
State Agriculture Biotechnology Centre, College of Science, Health, Engineering and Education, Murdoch University, Perth, WA, Australia.
School of Science, Edith Cowan University, Joondalup, WA, Australia.
Front Genet. 2020 Sep 30;11:583785. doi: 10.3389/fgene.2020.583785. eCollection 2020.
High nitrogen use efficiency (NUE) in bread wheat is pivotal to sustain high productivity. Knowledge about the physiological and transcriptomic changes that regulate NUE, in particular how plants cope with nitrogen (N) stress during flowering and the grain filling period, is crucial in achieving high NUE. Nitrogen response is differentially manifested in different tissues and shows significant genetic variability. A comparative transcriptome study was carried out using RNA-seq analysis to investigate the effect of nitrogen levels on gene expression at 0 days post anthesis (0 DPA) and 10 DPA in second leaf and grain tissues of three Australian wheat () varieties that were known to have varying NUEs. A total of 12,344 differentially expressed genes (DEGs) were identified under nitrogen stress where down-regulated DEGs were predominantly associated with carbohydrate metabolic process, photosynthesis, light-harvesting, and defense response, whereas the up-regulated DEGs were associated with nucleotide metabolism, proteolysis, and transmembrane transport under nitrogen stress. Protein-protein interaction and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways analysis further revealed that highly interacted down-regulated DEGs were involved in light-harvesting and photosynthesis, and up-regulated DEGs were mostly involved in steroid biosynthesis under N stress. The common down-regulated genes across the cultivars included photosystem II 10 kDa polypeptide family proteins, plant protein 1589 of uncharacterized protein function, etc., whereas common up-regulated genes included glutamate carboxypeptidase 2, placenta-specific8 (PLAC8) family protein, and a sulfate transporter. On the other hand, high NUE cultivar Mace responded to nitrogen stress by down-regulation of a stress-related gene annotated as beta-1,3-endoglucanase and pathogenesis-related protein (PR-4, PR-1) and up-regulation of MYB/SANT domain-containing RADIALIS (RAD)-like transcription factors. The medium NUE cultivar Spitfire and low NUE cultivar Volcani demonstrated strong down-regulation of Photosystem II 10 kDa polypeptide family protein and predominant up-regulation of 11S globulin seed storage protein 2 and protein transport protein Sec61 subunit gamma. In grain tissue, most of the DEGs were related to nitrogen metabolism and proteolysis. The DEGs with high abundance in high NUE cultivar can be good candidates to develop nitrogen stress-tolerant variety with improved NUE.
面包小麦的高氮利用效率(NUE)对于维持高生产力至关重要。了解调节NUE的生理和转录组变化,特别是植物在开花期和灌浆期如何应对氮(N)胁迫,对于实现高NUE至关重要。氮响应在不同组织中表现不同,并显示出显著的遗传变异性。利用RNA-seq分析进行了一项比较转录组研究,以调查氮水平对三个已知具有不同NUE的澳大利亚小麦品种的第二片叶子和籽粒组织在开花后0天(0 DPA)和10 DPA时基因表达的影响。在氮胁迫下共鉴定出12344个差异表达基因(DEG),其中下调的DEG主要与碳水化合物代谢过程、光合作用、光捕获和防御反应相关,而上调的DEG在氮胁迫下与核苷酸代谢、蛋白水解和跨膜运输相关。蛋白质-蛋白质相互作用和京都基因与基因组百科全书(KEGG)通路分析进一步表明,高度相互作用的下调DEG参与光捕获和光合作用,而上调的DEG在N胁迫下大多参与类固醇生物合成。不同品种间共同下调的基因包括光系统II 10 kDa多肽家族蛋白、功能未表征的植物蛋白1589等,而共同上调的基因包括谷氨酸羧肽酶2、胎盘特异性8(PLAC8)家族蛋白和一种硫酸盐转运蛋白。另一方面,高NUE品种Mace通过下调一个注释为β-1,3-内切葡聚糖酶和病程相关蛋白(PR-4、PR-1)的胁迫相关基因以及上调含MYB/SANT结构域的辐射状(RAD)样转录因子来响应氮胁迫。中等NUE品种Spitfire和低NUE品种Volcani表现出光系统II 10 kDa多肽家族蛋白的强烈下调以及11S球蛋白种子贮藏蛋白2和蛋白转运蛋白Sec61亚基γ的主要上调。在籽粒组织中,大多数DEG与氮代谢和蛋白水解相关。高NUE品种中高丰度的DEG可能是培育具有更高NUE的耐氮胁迫品种的良好候选基因。