Software College, Heilongjiang University, Harbin, 150080, China.
Software College, Heilongjiang University, Harbin, 150080, China.
Comput Biol Chem. 2018 Aug;75:1-10. doi: 10.1016/j.compbiolchem.2018.04.014. Epub 2018 Apr 22.
Sugar beet (Beta vulgaris) is an important crop of sugar production in the world. Previous studies reported that sugar beet monosomic addition line M14 obtained from the intercross between Beta vulgaris L. (cultivated species) and B. corolliflora Zoss (wild species) exhibited tolerance to salt (up to 0.5 M NaCl) stress. To estimate a broad spectrum of genes involved in the M14 salt tolerance will help elucidate the molecular mechanisms underlying salt stress. Comparative transcriptomics was performed to monitor genes differentially expressed in the leaf and root samples of the sugar beet M14 seedlings treated with 0, 200 and 400 mM NaCl, respectively. Digital gene expression revealed that 3856 unigenes in leaves and 7157 unigenes in roots were differentially expressed under salt stress. Enrichment analysis of the differentially expressed genes based on GO and KEGG databases showed that in both leaves and roots genes related to regulation of redox balance, signal transduction, and protein phosphorylation were differentially expressed. Comparison of gene expression in the leaf and root samples treated with 200 and 400 mM NaCl revealed different mechanisms for coping with salt stress. In addition, the expression levels of nine unigenes in the reactive oxygen species (ROS) scavenging system exhibited significant differences in the leaves and roots. Our transcriptomics results have provided new insights into the salt-stress responses in the leaves and roots of sugar beet.
甜菜(Beta vulgaris)是世界上重要的制糖作物。先前的研究报道,通过栽培种(Beta vulgaris L.)和野生种(B. corolliflora Zoss)杂交获得的甜菜单体附加系 M14 对盐(高达 0.5 M NaCl)胁迫具有耐受性。估计广泛参与 M14 耐盐性的基因有助于阐明盐胁迫的分子机制。为了监测甜菜 M14 幼苗叶片和根部在 0、200 和 400 mM NaCl 处理下差异表达的基因,进行了比较转录组学分析。数字基因表达显示,叶片中有 3856 个基因和根部中有 7157 个基因在盐胁迫下差异表达。基于 GO 和 KEGG 数据库的差异表达基因富集分析显示,叶片和根部中与氧化还原平衡、信号转导和蛋白磷酸化调节相关的基因均有差异表达。比较叶片和根部在 200 和 400 mM NaCl 处理下的基因表达,发现了应对盐胁迫的不同机制。此外,在活性氧(ROS)清除系统中的 9 个基因的表达水平在叶片和根部之间存在显著差异。我们的转录组学结果为甜菜叶片和根部的盐胁迫反应提供了新的见解。