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多组学综合分析为苜蓿耐碱机制提供了新视角。

Multi-omics integrative analysis provided new insights into alkaline stress in alfalfa.

机构信息

Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China; College of Life Science and Technology, Harbin Normal University, Harbin, 150025, China.

Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.

出版信息

Plant Physiol Biochem. 2024 Oct;215:109048. doi: 10.1016/j.plaphy.2024.109048. Epub 2024 Aug 18.

Abstract

Saline-alkali stress is one of the main abiotic stresses that limits plant growth. Salt stress has been widely studied, but alkaline salt degradation caused by NaHCO has rarely been investigated. In the present study, the alfalfa cultivar 'Zhongmu No. 1' was treated with 50 mM NaHCO (0, 4, 8, 12 and 24 h) to study the resulting enzyme activity and changes in mRNA, miRNA and metabolites in the roots. The results showed that the enzyme activity changed significantly after alkali stress treatment. The genomic analysis revealed 14,970 differentially expressed mRNAs (DEMs), 53 differentially expressed miRNAs (DEMis), and 463 differentially accumulated metabolites (DAMs). Combined analysis of DEMs and DEMis revealed that 21 DEMis negatively regulated 42 DEMs. In addition, when combined with Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis of DEMs and DAMs, we found that phenylpropanoid biosynthesis, flavonoid biosynthesis, starch and sucrose metabolism and plant hormone signal transduction played important roles in the alkali stress response. The results of this study further elucidated the regulatory mechanism underlying the plant response to alkali stress and provided valuable information for the breeding of new saline-alkaline tolerance plant varieties.

摘要

盐碱性胁迫是限制植物生长的主要非生物胁迫之一。盐胁迫已得到广泛研究,但很少研究由 NaHCO 引起的碱性盐降解。本研究以紫花苜蓿品种‘中苜 1 号’为材料,用 50 mM NaHCO(0、4、8、12 和 24 h)处理,研究其根系的酶活性变化和 mRNA、miRNA 和代谢物的变化。结果表明,碱胁迫处理后酶活性发生显著变化。基因组分析显示,有 14970 个差异表达的 mRNA(DEMs)、53 个差异表达的 miRNA(DEMis)和 463 个差异积累的代谢物(DAMs)。对 DEMs 和 DEMis 的综合分析表明,21 个 DEMis 负调控 42 个 DEMs。此外,当将 DEMs 和 DAMs 与京都基因与基因组百科全书(KEGG)分析相结合时,发现苯丙烷生物合成、类黄酮生物合成、淀粉和蔗糖代谢以及植物激素信号转导在碱胁迫响应中发挥重要作用。本研究的结果进一步阐明了植物对碱胁迫响应的调控机制,为培育新的耐盐碱性植物品种提供了有价值的信息。

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