Zhang Jingxia, Zhang Pei, Huo Xuehan, Gao Yang, Chen Yu, Song Zhangqiang, Wang Furong, Zhang Jun
Key Laboratory of Cotton Breeding and Cultivation in Huang-Huai-Hai Plain, Ministry of Agriculture, Cotton Research Center of Shandong Academy of Agricultural Sciences, Jinan, China.
Key Laboratory of Plant Stress Research, College of Life Sciences, Shandong Normal University, Jinan, China.
Front Plant Sci. 2021 Apr 13;12:639104. doi: 10.3389/fpls.2021.639104. eCollection 2021.
To understand the molecular mechanisms of salinity tolerance during seed germination and post-germination stages, this study characterized phenotypic and transcriptome responses of two cotton cultivars during salinity stress. The two cultivars were salt-tolerant (ST) LMY37 and salt-sensitive (SS) ZM12, with the former exhibiting higher germination rate, growth, and primary-root fresh weight under salinity stress. Transcriptomic comparison revealed that up-regulation of differentially expressed genes (DEGs) was the main characteristic of transcriptional regulation in ST, while SS DEGs were mainly down-regulated. GO and KEGG analyses uncovered both common and specific responses in ST and SS. Common processes, such as reactive oxygen species (ROS) metabolism and cell wall biosynthesis, may be general responses to salinity in cotton. In contrast, DEGs involved in MAPK-signaling pathway activated by ROS, carotenoid biosynthesis pathway and cysteine and methionine metabolism pathway [producing the precursors of stress hormone abscisic acid (ABA) and ethylene (ET), respectively] as well as stress tolerance related transcription factor genes, showed significant expression differences between ST and SS. These differences might be the molecular basis leading to contrasting salinity tolerance. Silencing of , an ethylene response factor gene, caused higher salinity sensitivity and increased ROS accumulation after salinity stress. In addition, peroxidase (POD) and superoxide dismutase (SOD) activity obviously declined after silencing . These results suggest that is involved in salinity tolerance during early development. This study provides a novel and comprehensive perspective to understand key mechanisms of salinity tolerance and explores candidate genes that may be useful in developing stress-tolerant crops through biotechnology.
为了解棉花种子萌发和萌发后阶段耐盐性的分子机制,本研究对两个棉花品种在盐胁迫下的表型和转录组反应进行了表征。这两个品种分别是耐盐(ST)的LMY37和盐敏感(SS)的ZM12,前者在盐胁迫下表现出更高的发芽率、生长量和初生根鲜重。转录组比较显示,差异表达基因(DEGs)上调是ST转录调控的主要特征,而SS中的DEGs主要下调。GO和KEGG分析揭示了ST和SS中常见和特异的反应。常见过程,如活性氧(ROS)代谢和细胞壁生物合成,可能是棉花对盐胁迫的普遍反应。相反,参与由ROS激活的MAPK信号通路、类胡萝卜素生物合成途径以及半胱氨酸和甲硫氨酸代谢途径(分别产生胁迫激素脱落酸(ABA)和乙烯(ET)的前体)的DEGs以及与胁迫耐受性相关的转录因子基因,在ST和SS之间表现出显著的表达差异。这些差异可能是导致耐盐性差异的分子基础。乙烯反应因子基因沉默后,盐敏感性增加,盐胁迫后ROS积累增加。此外,沉默后过氧化物酶(POD)和超氧化物歧化酶(SOD)活性明显下降。这些结果表明, 参与早期发育阶段的耐盐性。本研究为理解耐盐性的关键机制提供了一个新颖而全面的视角,并探索了可能有助于通过生物技术培育耐胁迫作物的候选基因。