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相互作用的MeZFP29和MebZIPW调节木薯中响应硝酸盐信号的MeNRT2.2。

Interacting MeZFP29 and MebZIPW regulates MeNRT2.2 from cassava responding to nitrate signaling.

作者信息

Li Wenbin, Yu Xiaoling, Zhao Pingjuan, Li Shuxia, Zou Liangping, Zhang Xiuchun, Li Jiuhui, Ruan Mengbin

机构信息

National Key Laboratory for Tropical Crop Breeding/Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture and Rural Affairs, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101, China.

Hainan Key Laboratory of Conservation and Utilization of Tropical Agricultural Biological Resources, Hainan Institute of Tropical Agricultural Resources, Haikou, China.

出版信息

Plant Cell Rep. 2025 Mar 4;44(3):69. doi: 10.1007/s00299-025-03455-4.

Abstract

Cassava is a significant tropical cash crop. MeZFP29 interacting with MebZIPW improves MeNRT2.2, encoding a high-affinity nitrate transporter, through binding to NREs under low nitrate and shows a nitrate-signaling-triggered regulation. Cassava (Manihot esculenta) is a globally significant tropical root crop and exhibits exceptional adaptability to native soil fertility. MeNRT2.2 encodes a high-affinity nitrate transporter in cassava and heterologous overexpression of MeNRT2.2 in Arabidopsis increases nitrate transportation and utilization under nitrogen scarcity. However, the responsive mechanism of MeNRT2.2 to nitrate remains unclear. In this study, we identified a nitrate-responsive fragment of 450 bp located upstream of the start codon of MeNRT2.2, and two potential regulators, MeZFP29 and MebZIPW, of MeNRT2.2. Two regulators specifically bound to nitrate-responsive cis-element (NRE), i.e., TGCATT and CAGATG, in the 450 bp fragment and together significantly stimulated promoter activity. Furthermore, we confirmed the interaction between two regulators in vivo and in vitro via Y2H, BiFC, Co-IP, and GST-pull-down assays. In addition, the distribution of MeZFP29 and its heterodimers (MeZFP&MebZIPW) are determined by nitrate signaling, i.e., in the cytoplasm and nucleus under nitrogen limitation, and predominantly in nucleus under sufficient nitrate. In contrast, MebZIPW consistently localizes to the cytoplasm and nucleus regardless of nitrate conditions. Moreover, overexpression of MeZFP29 in Arabidopsis enhanced growth and chlorophyll content, particularly, under low nitrate conditions, while MebZIPW did not. These findings not only confirm the regulation of MeZFP29 and MebZIPW on MeNRT2.2, but also illustrate the nitrate signaling-triggered promotion and feedback on MeNRT2.2. Our study provides a novel approach to enhancing nitrogen-use efficiency in cassava by modulating the regulators under moderate nitrogen levels as low as possible.

摘要

木薯是一种重要的热带经济作物。与MebZIPW相互作用的MeZFP29通过在低硝酸盐条件下与NRE结合来改善编码高亲和力硝酸盐转运蛋白的MeNRT2.2,并显示出硝酸盐信号触发的调控。木薯(Manihot esculenta)是一种全球重要的热带块根作物,对当地土壤肥力表现出非凡的适应性。MeNRT2.2在木薯中编码一种高亲和力硝酸盐转运蛋白,在拟南芥中异源过表达MeNRT2.2可增加氮缺乏条件下硝酸盐的运输和利用。然而,MeNRT2.2对硝酸盐的响应机制仍不清楚。在本研究中,我们鉴定了位于MeNRT2.2起始密码子上游450 bp的硝酸盐响应片段,以及MeNRT2.2的两个潜在调节因子MeZFP29和MebZIPW。两个调节因子特异性结合450 bp片段中的硝酸盐响应顺式元件(NRE),即TGCATT和CAGATG,并共同显著刺激启动子活性。此外,我们通过酵母双杂交、双分子荧光互补、免疫共沉淀和谷胱甘肽S-转移酶下拉试验在体内和体外证实了两个调节因子之间的相互作用。此外,MeZFP29及其异二聚体(MeZFP&MebZIPW)的分布由硝酸盐信号决定,即在氮限制条件下位于细胞质和细胞核中,在硝酸盐充足时主要位于细胞核中。相比之下,无论硝酸盐条件如何,MebZIPW始终定位于细胞质和细胞核。此外,在拟南芥中过表达MeZFP29可促进生长并提高叶绿素含量,特别是在低硝酸盐条件下,而MebZIPW则没有。这些发现不仅证实了MeZFP29和MebZIPW对MeNRT2.2的调控,还说明了硝酸盐信号对MeNRT2.2的触发促进和反馈作用。我们的研究提供了一种新方法,通过在尽可能低的适度氮水平下调节调节因子来提高木薯的氮利用效率。

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