Kong Xiangjun, Wang Rui, Jia Peipei, Li Hengbin, Khan Aziz, Muhammad Ali, Fiaz Sajid, Xing Qunce, Zhang Zhiyong
Henan Key Laboratory for Molecular Ecology and Germplasm Innovation of Cotton and Wheat and Xinxiang Key Laboratory of Crop Root Biology and Green Efficient Production, School of Life Sciences, Henan Collaborative Innovation Center of Modern Biological Breeding, Henan Institute of Science and Technology, Xinxiang, 453003, Henan, China.
Institute of Molecular Biology and Biotechnology, The University of Lahore, Lahore, 54590, Pakistan.
Plant Mol Biol. 2025 Jan 17;115(1):19. doi: 10.1007/s11103-024-01545-7.
Nitrogen (N) is a major plant nutrient and its deficiency can arrest plant growth. However, how low-N stress impair plant growth and its related tolerance mechanisms in peanut seedlings has not yet been explored. To counteract this issue, a hydroponic study was conducted to explore low N stress (0.1 mM NO) and normal (5.0 mM NO) effects on the morpho-physiological and molecular attributes of peanut seedlings. Low-N stress significantly decreased peanut plant height, leaf surface area, total root length, and primary root length after 10 days of treatment. Meanwhile, glutamate dehydrogenase, glutamine oxoglutarate aminotransferase activities, chlorophyll, and soluble protein contents were substantially decreased. Impairment in these parameters further suppressed photochemical efficiency (Fv/Fm), and chlorophyll fluorescence parameters (PI), under low-N stress. Transcriptome sequencing analysis showed a total of 2139 DEGs were identified between the two treatments. KEGG enrichment annotation analysis of DEGs revealed that 119 DEGs related to 10 pathways, including N assimilation, photosynthesis, starch, and sucrose degradation, which may respond to low-N stress in peanuts. Combined with transcriptome, small RNA, and degradome sequencing, we found that PC-3p-142756_56/A.T13EMM (CML3) and PC-5p-43940_274/A.81NSYN (YTH3) are the main modules contributing to low N stress tolerance in peanut crops. Peanut seedlings exposed to N starvation exhibited suppressed gene expression related to nitrate transport and assimilation, chlorophyll synthesis, and carbon assimilation, while also showing improved gene expression in N compensation/energy supply and carbohydrate consumption. Additionally, low N stress tolerance was strongly associated with the miRNA.
氮(N)是植物的主要养分,其缺乏会抑制植物生长。然而,低氮胁迫如何影响花生幼苗的生长及其相关耐受机制尚未得到探索。为了解决这个问题,开展了一项水培研究,以探究低氮胁迫(0.1 mM NO)和正常(5.0 mM NO)对花生幼苗形态生理和分子特性的影响。处理10天后,低氮胁迫显著降低了花生植株高度、叶表面积、总根长度和主根长度。同时,谷氨酸脱氢酶、谷氨酰胺酮戊二酸转氨酶活性、叶绿素和可溶性蛋白含量大幅下降。在低氮胁迫下,这些参数的损伤进一步抑制了光化学效率(Fv/Fm)和叶绿素荧光参数(PI)。转录组测序分析表明,两种处理之间共鉴定出2139个差异表达基因(DEG)。对DEG的KEGG富集注释分析显示,119个DEG与10条通路相关,包括氮同化、光合作用、淀粉和蔗糖降解,这些通路可能对花生的低氮胁迫作出响应。结合转录组、小RNA和降解组测序,我们发现PC-3p-142756_56/A.T13EMM(CML3)和PC-5p-43940_274/A.81NSYN(YTH3)是花生作物耐低氮胁迫的主要模块。暴露于氮饥饿的花生幼苗表现出与硝酸盐转运和同化、叶绿素合成以及碳同化相关的基因表达受到抑制,同时在氮补偿/能量供应和碳水化合物消耗方面的基因表达也有所改善。此外,低氮胁迫耐受性与miRNA密切相关。