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小麦Tae-MIR1118与钙调蛋白TaCaM2-1和MYB成员TaMYB44构成一个功能模块,以调节植物低氮胁迫反应。

Wheat Tae-MIR1118 Constitutes a Functional Module With Calmodulin TaCaM2-1 and MYB Member TaMYB44 to Modulate Plant Low-N Stress Response.

作者信息

Zhang Yanyang, Ma Chunying, Li Xiangqiang, Hou Xiaoyang, Wang Ziyi, Zhang Jiaqi, Zhang Chunlin, Shi Xinxin, Duan Wanrong, Guo Chengjin, Xiao Kai

机构信息

State Key Laboratory of North China Crop Improvement and Regulation, Baoding, Hebei, P.R. China.

College of Agronomy and Biotechnology, Hebei Normal University of Science & Technology, Qinhuangdao, Hebei, P.R. China.

出版信息

Plant Cell Environ. 2025 Mar;48(3):2178-2199. doi: 10.1111/pce.15285. Epub 2024 Nov 19.

Abstract

Distinct target genes are modulated by microRNA members and affect various biological processes associated with abiotic stress responses in plants. In this study, we characterized a functional module comprising miRNA/target and a downstream MYB transcription factor partner, Tae-MIR1118/TaCaM2/TaMYB44, in Triticum aestivum to mediate the plant low-nitrogen (N) stress response. Dual luciferase (LUC) assay and expression analysis indicated that TaCaM2 is regulated by Tae-MIR1118 through a posttranscriptional cleavage mechanism. Reporter LUC activity in N. benthamiana leaves co-transformed with effector CaMV35S::Tae-MIR1118 and reporter TaCaM2::LUC was significantly reduced, and the transcripts of Tae-MIR1118 and TaCaM2 in tissues exhibited converse expression patterns under varying N levels. Specifically, the transcripts of Tae-MIR1118 decreased, whereas those of TaCaM2 increased under low-N stress in a temporal-dependent manner. Yeast two-hybrid, bimolecular fluorescence complementation (BiFC) and co-immunoprecipitation (Co-IP) assays indicated that TaCaM2 interacted with the MYB transcription factor TaMYB44. Transgene analysis revealed the negative roles of Tae-MIR1118 and the positive functions of TaCaM2 and TaMYB44 in regulating plants for low-N stress adaptation by modulating glutamine synthetase activity, N uptake capacity, and root morphology. Yeast one-hybrid, transcriptional activation, and chromatin immunoprecipitation-quantitative polymerase chain reaction (ChIP-PCR) assays indicated that TaMYB44 could bind to the promoters of genes TaGS2.2, TaNRT2.1, and TaPIN4 and induce transcription of these stress-defensive genes. Knockdown of these three genes reduced GS activity, N accumulation, and root growth traits in plants subjected to N starvation. The yield in the wheat variety panel was highly correlated with the transcripts of Tae-MIR1118, TaCaM2, and TaMYB44 in plants cultured under N-deprived field conditions. A major haplotype of Tae-MIR1118, TaMIR1118-Hap1, enhanced the low-N stress tolerance of plants. Our findings indicate that the Tae-MIR1118/TaCaM2/TaMYB44 pathway primarily affects the low-N response of plants by modulating associated physiological processes.

摘要

不同的靶基因受微小RNA成员调控,并影响植物中与非生物胁迫反应相关的各种生物学过程。在本研究中,我们在普通小麦中鉴定了一个由微小RNA/靶标和下游MYB转录因子伴侣Tae-MIR1118/TaCaM2/TaMYB44组成的功能模块,以介导植物低氮胁迫反应。双荧光素酶(LUC)检测和表达分析表明,TaCaM2受Tae-MIR1118通过转录后切割机制调控。在与效应子CaMV35S::Tae-MIR1118和报告基因TaCaM2::LUC共转化的本氏烟草叶片中,报告基因LUC活性显著降低,并且在不同氮水平下,组织中Tae-MIR1118和TaCaM2的转录本呈现相反的表达模式。具体而言,在低氮胁迫下,Tae-MIR1118的转录本减少,而TaCaM2的转录本以时间依赖性方式增加。酵母双杂交、双分子荧光互补(BiFC)和免疫共沉淀(Co-IP)检测表明,TaCaM2与MYB转录因子TaMYB44相互作用。转基因分析揭示了Tae-MIR1118的负作用以及TaCaM2和TaMYB44通过调节谷氨酰胺合成酶活性、氮吸收能力和根系形态在调控植物适应低氮胁迫方面的正功能。酵母单杂交、转录激活和染色质免疫沉淀-定量聚合酶链反应(ChIP-PCR)检测表明,TaMYB44可以结合基因TaGS2.2、TaNRT2.1和TaPIN4的启动子并诱导这些胁迫防御基因的转录。敲低这三个基因会降低氮饥饿条件下植物的谷氨酰胺合成酶活性、氮积累和根系生长性状。在缺氮田间条件下培养的植物中,小麦品种面板中的产量与Tae-MIR1118、TaCaM2和TaMYB44的转录本高度相关。Tae-MIR1118的一个主要单倍型TaMIR1118-Hap增强了植物对低氮胁迫的耐受性。我们的研究结果表明,Tae-MIR1118/TaCaM2/TaMYB44途径主要通过调节相关生理过程来影响植物的低氮反应。

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