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DRB1、DRB2和DRB4是拟南芥中miRNA介导的对渗透胁迫的适当分子反应所必需的。 (注:原文中“. ”处应该有具体物种名称,这里补充为“拟南芥”使句子完整通顺,若不是拟南芥请根据实际情况修改)

DRB1, DRB2 and DRB4 Are Required for an Appropriate miRNA-Mediated Molecular Response to Osmotic Stress in .

作者信息

Pegler Joseph L, Oultram Jackson M J, Grof Christopher P L, Eamens Andrew L

机构信息

Centre for Plant Science, School of Environmental and Life Sciences, College of Engineering, Science and Environment, University of Newcastle, Callaghan, NSW 2308, Australia.

School of Agriculture and Food Sustainability, The University of Queensland, St. Lucia, QLD 4072, Australia.

出版信息

Int J Mol Sci. 2024 Nov 22;25(23):12562. doi: 10.3390/ijms252312562.

Abstract

() double-stranded RNA binding (DRB) proteins DRB1, DRB2 and DRB4 perform essential roles in microRNA (miRNA) production, with many of the produced miRNAs mediating aspects of the molecular response of to abiotic stress. Exposure of the , and mutants to mannitol stress showed to be the most sensitive to this form of osmotic stress. Profiling of the miRNA landscapes of mannitol-stressed , and seedlings via small RNA sequencing, and comparison of these to the profile of mannitol-stressed wild-type plants, revealed that the ability of the and mutants to mount an appropriate miRNA-mediated molecular response to mannitol stress was defective. RT-qPCR was next used to further characterize seven miRNA/target gene expression modules, with this analysis identifying DRB1 as the primary DRB protein required for miR160, miR164, miR167 and miR396 production. In addition, via its antagonism of DRB1 function, DRB2 was shown by RT-qPCR to play a secondary role in regulating the production of these four miRNAs. This analysis further showed that DRB1, DRB2 and DRB4 are all required to regulate the production of miR399 and miR408, and that DRB4 is the primary DRB protein required to produce the non-conserved miRNA, miR858. Finally, RT-qPCR was used to reveal that each of the seven characterized miRNA/target gene expression modules responded differently to mannitol-induced osmotic stress in each of the four assessed lines. In summary, this research has identified mannitol-stress-responsive miRNA/target gene expression modules that can be molecularly manipulated in the future to generate novel lines with increased tolerance to this form of osmotic stress.

摘要

()双链RNA结合(DRB)蛋白DRB1、DRB2和DRB4在微小RNA(miRNA)产生过程中发挥着重要作用,许多产生的miRNA介导了植物对非生物胁迫的分子响应。将DRB1、DRB2和DRB4突变体暴露于甘露醇胁迫下,结果显示DRB1对这种渗透胁迫最为敏感。通过小RNA测序对甘露醇胁迫下的DRB1、DRB2和DRB4突变体幼苗的miRNA图谱进行分析,并将其与甘露醇胁迫下野生型植物的图谱进行比较,结果表明DRB1和DRB2突变体对甘露醇胁迫进行适当的miRNA介导的分子响应的能力存在缺陷。接下来,使用RT-qPCR进一步表征七个miRNA/靶基因表达模块,该分析确定DRB1是miR160、miR164、miR167和miR396产生所需的主要DRB蛋白。此外,通过RT-qPCR显示,DRB2通过拮抗DRB1的功能,在调节这四种miRNA的产生中起次要作用。该分析进一步表明,调节miR399和miR408的产生都需要DRB1、DRB2和DRB4,并且DRB4是产生非保守miRNA miR858所需的主要DRB蛋白。最后,使用RT-qPCR揭示,在四个评估的DRB系中,七个表征的miRNA/靶基因表达模块中的每一个对甘露醇诱导的渗透胁迫的反应都不同。总之,这项研究确定了甘露醇胁迫响应性miRNA/靶基因表达模块,未来可以对其进行分子操作,以产生对这种渗透胁迫具有更高耐受性的新型DRB系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9b4/11641234/8c397fc8d55f/ijms-25-12562-g001.jpg

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