Li Ning, Wang Zhongyu, Wang Baike, Wang Juan, Xu Ruiqiang, Yang Tao, Huang Shaoyong, Wang Huan, Yu Qinghui
Institute of Horticulture Crops, Xinjiang Academy of Agricultural Sciences, Urumqi, China.
Key Laboratory of Horticulture Crop Genomics and Genetic Improvement in Xinjiang, Urumqi, China.
Front Plant Sci. 2022 Jul 4;13:834027. doi: 10.3389/fpls.2022.834027. eCollection 2022.
As one of the most important vegetable crops in the world, the production of tomatoes was restricted by salt stress. Therefore, it is of great interest to analyze the salt stress tolerance genes. As the non-coding RNAs (ncRNAs) with a length of more than 200 nucleotides, long non-coding RNAs (lncRNAs) lack the ability of protein-coding, but they can play crucial roles in plant development and response to abiotic stresses by regulating gene expression. Nevertheless, there are few studies on the roles of salt-induced lncRNAs in tomatoes. Therefore, we selected wild tomato () and cultivated tomato M82 to be materials. By high-throughput sequencing, 1,044 putative lncRNAs were identified here. Among them, 154 and 137 lncRNAs were differentially expressed in M82 and , respectively. Through functional analysis of target genes of differentially expressed lncRNAs (DE-lncRNAs), some genes were found to respond positively to salt stress by participating in abscisic acid (ABA) signaling pathway, brassinosteroid (BR) signaling pathway, ethylene (ETH) signaling pathway, and anti-oxidation process. We also construct a salt-induced lncRNA-mRNA co-expression network to dissect the putative mechanisms of high salt tolerance in . We analyze the function of salt-induced lncRNAs in tomato roots at the genome-wide levels for the first time. These results will contribute to understanding the molecular mechanisms of salt tolerance in tomatoes from the perspective of lncRNAs.
作为世界上最重要的蔬菜作物之一,番茄的产量受到盐胁迫的限制。因此,分析耐盐胁迫基因具有重要意义。长链非编码RNA(lncRNA)作为长度超过200个核苷酸的非编码RNA(ncRNA),缺乏蛋白质编码能力,但它们可以通过调控基因表达在植物发育和对非生物胁迫的响应中发挥关键作用。然而,关于盐诱导的lncRNA在番茄中的作用的研究很少。因此,我们选择野生番茄()和栽培番茄M82作为材料。通过高通量测序,在此鉴定出1044个假定的lncRNA。其中,分别有154个和137个lncRNA在M82和中差异表达。通过对差异表达lncRNA(DE-lncRNA)的靶基因进行功能分析,发现一些基因通过参与脱落酸(ABA)信号通路、油菜素内酯(BR)信号通路、乙烯(ETH)信号通路和抗氧化过程对盐胁迫产生积极响应。我们还构建了一个盐诱导的lncRNA-mRNA共表达网络,以剖析(此处原文缺失具体品种名)高耐盐性的假定机制。我们首次在全基因组水平上分析了盐诱导的lncRNA在番茄根中的功能。这些结果将有助于从lncRNA的角度理解番茄耐盐性的分子机制。