Yao Xiao-Cui, Meng Li-Fang, Zhao Wang-Li, Mao Gui-Lian
School of Life Sciences, Ningxia University, Yinchuan, China.
Front Plant Sci. 2023 Feb 20;14:1090366. doi: 10.3389/fpls.2023.1090366. eCollection 2023.
Salt stress directly affects the growth of plants. The limitation of leaf grow is among the earliest visible effects of salt stress. However, the regulation mechanism of salt treatments on leaf shape has not been fully elucidated. We measured the morphological traits and anatomical structure. In combination with transcriptome analysis, we analyzed differentially expressed genes (DEGs) and verified the RNA-seq data by qRT-PCR. Finally, we analyzed correlation between leaf microstructure parameters and expansin genes. We show that the leaf thickness, the width, and the leaf length significantly increased at elevated salt concentrations after salt stress for 7 days. Low salt mainly promoted the increase in leaves length and width, but high salt concentration accelerated the leaf thickness. The anatomical structure results indicated that palisade mesophyll tissues contribute more to leaf thickness than spongy mesophyll tissues, which possibly contributed to the increase in leaf expansion and thickness. Moreover, a total of 3,572 DEGs were identified by RNA-seq. Notably, six of the DEGs among 92 identified genes concentrated on cell wall synthesis or modification were involved in cell wall loosening proteins. More importantly, we demonstrated that there was a strong positive correlation between the upregulated gene and the thickness of the palisade tissue in leaves. These results suggested that salt stress possibly induced the expression of gene, which in turn increased the thickness of leaves by promoting the longitudinal expansion of cells of the palisade tissue. This study lays a solid knowledge for revealing the underlying molecular mechanisms of leaf thickening in in response to salt stresses.
盐胁迫直接影响植物的生长。叶片生长受限是盐胁迫最早可见的影响之一。然而,盐处理对叶片形状的调控机制尚未完全阐明。我们测量了形态特征和解剖结构。结合转录组分析,我们分析了差异表达基因(DEGs),并通过qRT-PCR验证了RNA-seq数据。最后,我们分析了叶片微观结构参数与扩张蛋白基因之间的相关性。我们发现,盐胁迫7天后,在盐浓度升高时,叶片厚度、宽度和长度显著增加。低盐主要促进叶片长度和宽度的增加,但高盐浓度加速了叶片厚度的增加。解剖结构结果表明,栅栏叶肉组织对叶片厚度的贡献大于海绵叶肉组织,这可能有助于叶片扩展和厚度增加。此外,通过RNA-seq鉴定出总共3572个DEGs。值得注意的是,在92个已鉴定的基因中,有6个DEGs集中在细胞壁合成或修饰上,它们参与细胞壁松弛蛋白的合成。更重要的是,我们证明上调基因与叶片栅栏组织厚度之间存在很强的正相关。这些结果表明,盐胁迫可能诱导了该基因的表达,进而通过促进栅栏组织细胞的纵向扩张增加了叶片厚度。本研究为揭示[植物名称]响应盐胁迫时叶片增厚的潜在分子机制奠定了坚实的知识基础。