College of Agriculture, Fujian Agriculture and Forestry University, No. 15 Shangxiadian Road, Cangshan District, Fuzhou, 350002, People's Republic of China.
Guangxi key Laboratory of Medicinal Resources Protection and Genetic Improvement, Guangxi Botanical Garden of Medicinal Plants, No. 189 Changgang Road, Xingning District, Nanning, 530023, People's Republic of China.
BMC Plant Biol. 2021 Dec 2;21(1):566. doi: 10.1186/s12870-021-03334-6.
Sophora tonkinensis Gagnep is a traditional Chinese medical plant that is mainly cultivated in southern China. Drought stress is one of the major abiotic stresses that negatively impacts S. tonkinensis growth. However, the molecular mechanisms governing the responses to drought stress in S. tonkinensis at the transcriptional and posttranscriptional levels are not well understood.
To identify genes and miRNAs involved in drought stress responses in S. tonkinensis, both mRNA and small RNA sequencing was performed in root samples under control, mild drought, and severe drought conditions. mRNA sequencing revealed 66,476 unigenes, and the differentially expressed unigenes (DEGs) were associated with several key pathways, including phenylpropanoid biosynthesis, sugar metabolism, and quinolizidine alkaloid biosynthesis pathways. A total of 10 and 30 transcription factors (TFs) were identified among the DEGs under mild and severe drought stress, respectively. Moreover, small RNA sequencing revealed a total of 368 miRNAs, including 255 known miRNAs and 113 novel miRNAs. The differentially expressed miRNAs and their target genes were involved in the regulation of plant hormone signal transduction, the spliceosome, and ribosomes. Analysis of the regulatory network involved in the response to drought stress revealed 37 differentially expressed miRNA-mRNA pairs.
This is the first study to simultaneously profile the expression patterns of mRNAs and miRNAs on a genome-wide scale to elucidate the molecular mechanisms of the drought stress responses of S. tonkinensis. Our results suggest that S. tonkinensis implements diverse mechanisms to modulate its responses to drought stress.
苦参是一种传统的中药植物,主要在中国南方种植。干旱胁迫是影响苦参生长的主要非生物胁迫之一。然而,苦参在转录和转录后水平上对干旱胁迫的响应的分子机制尚不清楚。
为了鉴定苦参响应干旱胁迫的基因和 miRNA,在对照、轻度干旱和重度干旱条件下对苦参根样进行了 mRNA 和小 RNA 测序。mRNA 测序共鉴定出 66476 条 unigenes,差异表达 unigenes(DEGs)与几个关键途径有关,包括苯丙烷生物合成、糖代谢和喹诺里西啶生物碱生物合成途径。在轻度和重度干旱胁迫下,分别鉴定到 10 和 30 个转录因子(TFs)。此外,小 RNA 测序共鉴定到 368 个 miRNA,包括 255 个已知 miRNA 和 113 个新 miRNA。差异表达的 miRNA 及其靶基因参与植物激素信号转导、剪接体和核糖体的调控。对参与干旱胁迫响应的调控网络的分析揭示了 37 个差异表达的 miRNA-mRNA 对。
这是首次在全基因组范围内同时分析 mRNA 和 miRNA 的表达模式,阐明苦参对干旱胁迫响应的分子机制。我们的研究结果表明,苦参采用多种机制来调节其对干旱胁迫的响应。