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

IF 6 1区 生物学 Q1 PLANT SCIENCES Plant, Cell & Environment Pub Date : 2024-11-19 DOI:10.1111/pce.15285
Yanyang Zhang, Chunying Ma, Xiangqiang Li, Xiaoyang Hou, Ziyi Wang, Jiaqi Zhang, Chunlin Zhang, Xinxin Shi, Wanrong Duan, Chengjin Guo, Kai Xiao
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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.

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小麦 Tae-MIR1118 与钙调蛋白 TaCaM2-1 和 MYB 成员 TaMYB44 组成一个功能模块,共同调节植物的低氮胁迫反应。
不同的靶基因受 microRNA 成员的调控,并影响与植物非生物胁迫反应相关的各种生物过程。在这项研究中,我们鉴定了一个由 miRNA/靶标和下游 MYB 转录因子伙伴 Tae-MIR1118/TaCaM2/TaMYB44 组成的功能模块,该模块在小麦中介导植物的低氮(N)胁迫响应。双荧光素酶(LUC)测定和表达分析表明,TaCaM2 通过转录后裂解机制受 Tae-MIR1118 的调控。用效应物 CaMV35S::Tae-MIR1118 和报告物 TaCaM2::LUC 共同转化的 N. benthamiana 叶片中报告物 LUC 活性显著降低,组织中 Tae-MIR1118 和 TaCaM2 的转录本在不同 N 水平下表现出相反的表达模式。具体来说,在低氮胁迫下,Tae-MIR1118的转录本减少,而TaCaM2的转录本则以时间依赖的方式增加。酵母双杂交、双分子荧光互补(BiFC)和共免疫沉淀(Co-IP)分析表明,TaCaM2与MYB转录因子TaMYB44相互作用。转基因分析表明,Tae-MIR1118 在通过调节谷氨酰胺合成酶活性、氮吸收能力和根系形态来调控植物对低氮胁迫的适应方面具有负作用,而 TaCaM2 和 TaMYB44 则具有正功能。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能与基因TaGS2.2、TaNRT2.1和TaPIN4的启动子结合,并诱导这些胁迫防御基因的转录。敲除这三个基因可降低氮饥饿植物的 GS 活性、氮积累和根系生长性状。在缺氮的田间条件下培养的植物中,小麦品种组的产量与 Tae-MIR1118、TaCaM2 和 TaMYB44 的转录本高度相关。Tae-MIR1118 的一个主要单倍型 TaMIR1118-Hap1 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响应。
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来源期刊
Plant, Cell & Environment
Plant, Cell & Environment 生物-植物科学
CiteScore
13.30
自引率
4.10%
发文量
253
审稿时长
1.8 months
期刊介绍: Plant, Cell & Environment is a premier plant science journal, offering valuable insights into plant responses to their environment. Committed to publishing high-quality theoretical and experimental research, the journal covers a broad spectrum of factors, spanning from molecular to community levels. Researchers exploring various aspects of plant biology, physiology, and ecology contribute to the journal's comprehensive understanding of plant-environment interactions.
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