Department of Systems Biology, Agricultural Research, Education and Extension Organization (AREEO), Agricultural Biotechnology Research Institute of Iran (ABRII), PO Box 31535-1897, Karaj, Iran.
Sci Rep. 2022 Dec 15;12(1):21696. doi: 10.1038/s41598-022-26133-x.
Salinity seriously constrains growth and fertility of rice worldwide. Long non-coding RNAs (lncRNAs) play crucial roles in plant abiotic stress response. However, salt responsive lncRNAs are poorly understood in rice. Herein, salt responsive lncRNAs (DE-lncRNAs) were identified in FL478 (salt tolerant) compared to its susceptible parent (IR29) using RNA-seq in root tissues at seedling stage. In FL478 and IR29, 8724 and 9235 transcripts with length of > 200 bp were nominated as potential lncRNAs, respectively. Rigorous filtering left four (in FL478) and nine (in IR29) DE-lncRNAs with only 2 DE-lncRNAs in common. ATAC-seq data showed that the genomic regions of all four lncRNAs in FL478 and 6/9 in IR29 are significantly accessible for transcription. Weighted correlation network analysis (WGCNA) revealed that lncRNA.2-FL was highly correlated with 173 mRNAs as trans-targets and a gene encoding pentatricopeptide repeat (PPR) protein was predicted as cis-target of lncRNA.2-FL. In silico mutagenesis analysis proposed the same transcription factor binding sites (TFBSs) in vicinity of the trans- and cis-regulatory target genes of lncRNA.2-FL, which significantly affect their transcription start site (TSS). This study provides new insights into involvement of the DE-lncRNAs in rice response to salt stress. Among them, lncRNA.2-FL may play a significant regulatory role in the salt stress tolerance of FL478.
盐度严重限制了全球水稻的生长和产量。长链非编码 RNA(lncRNA)在植物非生物胁迫响应中发挥着关键作用。然而,水稻中盐响应的 lncRNA 知之甚少。本研究利用 RNA-seq 在幼苗期根组织中比较耐盐品种 FL478 与其感盐亲本 IR29 ,鉴定了盐响应的 lncRNA(DE-lncRNA)。在 FL478 和 IR29 中,分别提名了 8724 个和 9235 个长度大于 200bp 的转录本作为潜在的 lncRNA。严格筛选后,FL478 中只剩下 4 个 DE-lncRNA,IR29 中只剩下 9 个 DE-lncRNA,其中只有 2 个 DE-lncRNA是共有的。ATAC-seq 数据表明,FL478 中所有 4 个 lncRNA 和 IR29 中 6/9 个 lncRNA 的基因组区域都可显著转录。加权相关网络分析(WGCNA)显示,lncRNA.2-FL 与 173 个 mRNA 作为反式靶标高度相关,并预测一个编码五肽重复(PPR)蛋白的基因为 lncRNA.2-FL 的顺式靶标。计算机诱变分析提出了 lncRNA.2-FL 的反式和顺式调控靶基因附近相同的转录因子结合位点(TFBSs),这显著影响了它们的转录起始位点(TSS)。本研究为 DE-lncRNA 参与水稻盐胁迫反应提供了新的见解。其中,lncRNA.2-FL 可能在 FL478 耐盐性中发挥重要的调控作用。