MicroRNA responses to alkaline stress and the key role of the miR156–MsSPL2/6B module in alfalfa

IF 5.7 2区 生物学 Q1 PLANT SCIENCES
Tongtong Yao , Siyue Qi , Hongjiao Zhang , Hongrui Zhang , Jiang Su , Zhongyong Cen , Zheyuan Wang , Bo Qin , Huihui Zhang
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引用次数: 0

Abstract

The global expansion of saline-alkali soils has made alkaline stress a major abiotic factor limiting plant growth and crop yield. Alfalfa (Medicago sativa L.), as an important high-quality forage grass, also has its growth and development significantly been constrained by alkaline stress. To investigate the molecular mechanisms underlying alfalfa's response to alkaline stress, this study focused on two previously identified alfalfa cultivars with distinct tolerance levels: the tolerant “ZD (Zhaodong)” and the sensitive “ZM (Zhongmu No.1).” Using miRNA-Seq and RNA-Seq, we systematically analyzed the expression changes of miRNAs and mRNAs in both cultivars under alkaline stress, aiming to identify key regulatory miRNAs and their target gene modules. The analysis identified 112 miRNAs that were significantly differentially expressed miRNAs (DEMs) following NaHCO3 treatment. Integrative miRNA-mRNA analysis revealed 258 high-confidence miRNA-target gene interaction pairs. Functional enrichment of DEMs and differentially expressed genes (DEGs) highlighted several biological processes and signaling pathways closely associated with stress response, including transcription factor regulation, phenylpropanoid biosynthesis, flavonoid metabolism, plant hormone signaling, and calcium (Ca2+) signaling. Notably, many genes related to hormone and Ca2+ signaling were reportedly regulated by differentially expressed miRNAs, exhibiting significant expression differences between the two cultivars. This underscores their critical role in balancing growth and stress response. Additionally, numerous differentially expressed miRNAs indirectly regulate alfalfa's alkaline tolerance by targeting transcription factors, with the miR156-SPL module identified as a potentially key contributor to alkaline stress adaptation. Transient co-expression assays demonstrated that Ms-miR156 target to MsSPL2 and MsSPL6B. Overexpression of MsSPL2 and MsSPL6B in Arabidopsis enhanced tolerance to alkaline stress, alleviating its adverse effects on root growth, photoinhibition, and oxidative damage. In summary, this study systematically elucidates the miRNA-mediated regulatory network underlying alfalfa's response to alkaline stress, providing a theoretical foundation and potential molecular targets for understanding and improving salt-alkali tolerance in alfalfa.
紫花苜蓿对碱性胁迫的MicroRNA响应及miR156-MsSPL2/6B模块的关键作用
全球盐碱地的扩张使碱性胁迫成为限制植物生长和作物产量的主要非生物因子。紫花苜蓿(Medicago sativa L.)作为重要的优质牧草,其生长发育也明显受到碱胁迫的制约。为了探究紫花苜蓿对碱性胁迫响应的分子机制,本研究以两个已鉴定的耐碱性水平不同的紫花苜蓿品种“ZD(肇东)”和“ZM(中牧1号)”为研究对象。我们利用miRNA-Seq和RNA-Seq技术,系统分析了两个品种在碱性胁迫下mirna和mrna的表达变化,旨在鉴定关键调控mirna及其靶基因模块。分析发现112个mirna在NaHCO3处理后显著表达差异mirna (dem)。综合miRNA-mRNA分析显示258对高置信度的mirna -靶基因相互作用对。dem和差异表达基因(DEGs)的功能富集突出了与胁迫反应密切相关的几种生物过程和信号通路,包括转录因子调节、苯丙类生物合成、类黄酮代谢、植物激素信号传导和钙(Ca2+)信号传导。值得注意的是,据报道,许多与激素和Ca2+信号相关的基因受差异表达的mirna调控,在两个品种之间表现出显著的表达差异。这强调了它们在平衡生长和应激反应方面的关键作用。此外,许多差异表达的mirna通过靶向转录因子间接调节苜蓿的碱性耐受性,其中miR156-SPL模块被认为是碱性胁迫适应的潜在关键因素。瞬时共表达实验表明Ms-miR156靶向MsSPL2和MsSPL6B。过表达MsSPL2和MsSPL6B可增强拟南芥对碱性胁迫的耐受性,减轻其对根系生长、光抑制和氧化损伤的不利影响。综上所述,本研究系统阐明了紫花苜蓿对碱性胁迫响应的mirna调控网络,为了解和提高紫花苜蓿的耐盐碱性提供了理论基础和潜在的分子靶点。
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来源期刊
Plant Physiology and Biochemistry
Plant Physiology and Biochemistry 生物-植物科学
CiteScore
11.10
自引率
3.10%
发文量
410
审稿时长
33 days
期刊介绍: Plant Physiology and Biochemistry publishes original theoretical, experimental and technical contributions in the various fields of plant physiology (biochemistry, physiology, structure, genetics, plant-microbe interactions, etc.) at diverse levels of integration (molecular, subcellular, cellular, organ, whole plant, environmental). Opinions expressed in the journal are the sole responsibility of the authors and publication does not imply the editors'' agreement. Manuscripts describing molecular-genetic and/or gene expression data that are not integrated with biochemical analysis and/or actual measurements of plant physiological processes are not suitable for PPB. Also "Omics" studies (transcriptomics, proteomics, metabolomics, etc.) reporting descriptive analysis without an element of functional validation assays, will not be considered. Similarly, applied agronomic or phytochemical studies that generate no new, fundamental insights in plant physiological and/or biochemical processes are not suitable for publication in PPB. Plant Physiology and Biochemistry publishes several types of articles: Reviews, Papers and Short Papers. Articles for Reviews are either invited by the editor or proposed by the authors for the editor''s prior agreement. Reviews should not exceed 40 typewritten pages and Short Papers no more than approximately 8 typewritten pages. The fundamental character of Plant Physiology and Biochemistry remains that of a journal for original results.
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