Research Institute of Tropical Forestry, Chinese Academy of Forestry, 682 Guangshan Road 1, Guangzhou 510520, China.
Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Forest Genetics and Biotechnology Ministry of Education, College of Forestry, Nanjing Forestry University, 159 Longpan Road, Nanjing 210037, China.
Int J Mol Sci. 2023 Sep 28;24(19):14655. doi: 10.3390/ijms241914655.
Masson pine ( Lamb.) is a major fast-growing woody tree species and pioneer species for afforestation in barren sites in southern China. However, the regulatory mechanism of gene expression in under drought remains unclear. To uncover candidate microRNAs, their expression profiles, and microRNA-mRNA interactions, small RNA-seq was used to investigate the transcriptome from seedling roots under drought and rewatering in . A total of 421 plant microRNAs were identified. Pairwise differential expression analysis between treatment and control groups unveiled 134, 156, and 96 differential expressed microRNAs at three stages. These constitute 248 unique microRNAs, which were subsequently categorized into six clusters based on their expression profiles. Degradome sequencing revealed that these 248 differentially expressed microRNAs targeted 2069 genes. Gene Ontology enrichment analysis suggested that these target genes were related to translational and posttranslational regulation, cell wall modification, and reactive oxygen species scavenging. miRNAs such as miR482, miR398, miR11571, miR396, miR166, miRN88, and miRN74, along with their target genes annotated as F-box/kelch-repeat protein, 60S ribosomal protein, copper-zinc superoxide dismutase, luminal-binding protein, S-adenosylmethionine synthase, and may play critical roles in drought response. This study provides insights into microRNA responsive to drought and rewatering in Masson pine and advances the understanding of drought tolerance mechanisms in .
马尾松(Lamb.)是中国南方荒山造林的主要速生用材树种和先锋树种。然而,其在干旱条件下基因表达的调控机制尚不清楚。为了揭示候选 microRNA,及其表达谱和 microRNA-mRNA 相互作用,本研究利用小 RNA-seq 技术研究了干旱和复水条件下马尾松幼苗根系的转录组。共鉴定出 421 种植物 microRNA。处理组和对照组之间的成对差异表达分析揭示了在三个阶段分别有 134、156 和 96 个差异表达的 microRNA。这些构成了 248 个独特的 microRNA,随后根据它们的表达谱分为六个簇。降解组测序显示,这 248 个差异表达的 microRNA 靶向了 2069 个基因。基因本体论富集分析表明,这些靶基因与翻译和翻译后调控、细胞壁修饰和活性氧清除有关。miR482、miR398、miR11571、miR396、miR166、miR88 和 miR74 等 microRNA 及其注释为 F-box/kelch-repeat 蛋白、60S 核糖体蛋白、铜锌超氧化物歧化酶、腔结合蛋白、S-腺苷甲硫氨酸合成酶和的靶基因,可能在干旱响应中发挥关键作用。本研究为马尾松对干旱和复水响应的 microRNA 提供了新的见解,同时也加深了对马尾松耐旱机制的理解。