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苹果模块通过整合抗坏血酸代谢增强干旱胁迫耐受性。

The Apple Module Enhances Drought Stress Tolerance by Integrating Ascorbic Acid Metabolism.

机构信息

Department of Pomology, College of Horticulture, China Agricultural University, Beijing 100193, China.

Department of Pomology, College of Horticulture, China Agricultural University, Beijing 100193, China

出版信息

Plant Physiol. 2020 Sep;184(1):194-211. doi: 10.1104/pp.20.00476. Epub 2020 Jul 17.

DOI:10.1104/pp.20.00476
PMID:32680976
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7479918/
Abstract

Drought stress severely restricts crop yield and quality. Small noncoding RNAs play critical roles in plant growth, development, and stress responses by regulating target gene expression, but their roles in drought stress tolerance in apple () are poorly understood. Here, we identified various small noncoding RNAs and their targets from the wild apple species via high-throughput sequencing and degradome analysis. Forty known microRNAs (miRNAs) and eight new small noncoding RNAs were differentially expressed in response to 2 or 4 h of drought stress treatment. We experimentally verified the expression patterns of five selected miRNAs and their targets. We established that one miRNA, mdm-miR171i, specifically targeted and degraded - ( ) transcripts. Both knockout of - and overexpression of improved drought stress tolerance in the cultivated apple line 'GL-3' by regulating the expression of antioxidant enzyme genes, especially that of , which functions in metabolism under drought stress. Transient expression analysis demonstrated that MsSCL26.1 activates transcription by positively regulating the activity of the region in its promoter. Therefore, the - module enhances drought stress tolerance in apple by regulating antioxidant gene expression and ascorbic acid metabolism.

摘要

干旱胁迫严重限制了作物的产量和品质。小非编码 RNA 通过调控靶基因的表达,在植物的生长、发育和应激反应中发挥着关键作用,但它们在苹果中对干旱胁迫耐受性的作用还知之甚少。在这里,我们通过高通量测序和降解组分析,从野生苹果中鉴定出了各种小非编码 RNA 及其靶标。在 2 或 4 小时的干旱胁迫处理下,有 40 个已知的 microRNAs(miRNAs)和 8 个新的小非编码 RNA 呈现出差异表达。我们通过实验验证了 5 个选定的 miRNAs 和它们的靶标表达模式。我们确定了一个 miRNA,mdm-miR171i,特异性地靶向并降解了 的转录本。敲除 和过表达 都通过调节抗氧化酶基因的表达,特别是在干旱胁迫下发挥作用的 基因的表达,改善了栽培苹果品种 'GL-3' 的耐旱性。瞬时表达分析表明,MsSCL26.1 通过正向调节其启动子中的 区域的活性来激活 转录。因此,- 模块通过调节抗氧化基因表达和抗坏血酸代谢来增强苹果的耐旱性。