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AP2/ERF转录因子ERF56对硝酸盐依赖的植物生长起负调控作用 。

The AP2/ERF Transcription Factor ERF56 Negatively Regulating Nitrate-Dependent Plant Growth in .

作者信息

Yao Guoqi, Mu Chunhua, Yan Zhenwei, Ma Shijun, Liu Xia, Sun Yue, Hou Jing, Liu Qiantong, Cao Bing, Shan Juan, Leng Bingying

机构信息

Maize Research Institute, Shandong Academy of Agricultural Sciences, Jinan 250100, China.

College of Agronomy, Qingdao Agricultural University, Qingdao 266109, China.

出版信息

Int J Mol Sci. 2025 Jan 13;26(2):613. doi: 10.3390/ijms26020613.

Abstract

ERF56, a member of the APETALA2/ETHYLENE-RESPONSIVE FACTOR (AP2/ERF) transcription factor (TF) family, was reported to be an early nitrate-responsive TF in . But the function of in nitrate signaling remains not entirely clear. This study aimed to investigate the role of in nitrate-dependent plant growth and nitrate signaling. We confirmed with reverse transcription quantitative PCR (RT-qPCR) that the transcription of is quickly induced by nitrate. overexpressors displayed decreased nitrate-dependent plant growth, while mutants exhibited increased plant growth. Confocal imaging demonstrated that ERF56 is localized into nuclei. Assays with the glucuronidase (GUS) reporter showed that is mainly expressed at the region of maturation of roots and in anthers. The dual-luciferase assay manifested that the transcription of is not directly regulated by NIN-LIKE PROTEIN 7 (NLP7). The transcriptome analysis identified 1038 candidate genes regulated by ERF56 directly. A gene ontology (GO) over-representation analysis showed that is involved in the processes of water transport, inorganic molecule transmembrane transport, secondary metabolite biosynthesis, and cell wall organization. We revealed that represses nitrate-dependent growth through regulating the processes of inorganic molecule transmembrane transport, the secondary metabolite biosynthesis, and cell wall organization.

摘要

ERF56是APETALA2/乙烯响应因子(AP2/ERF)转录因子家族的成员之一,据报道它是一种早期硝酸盐响应转录因子。但它在硝酸盐信号传导中的功能仍不完全清楚。本研究旨在探究其在硝酸盐依赖的植物生长和硝酸盐信号传导中的作用。我们通过逆转录定量PCR(RT-qPCR)证实,ERF56的转录可被硝酸盐快速诱导。ERF56过表达植株表现出硝酸盐依赖的植物生长减弱,而ERF56突变体则表现出植物生长增强。共聚焦成像显示ERF56定位于细胞核。利用葡糖醛酸糖苷酶(GUS)报告基因的分析表明,ERF56主要在根的成熟区和花药中表达。双荧光素酶测定表明,ERF56的转录不受类NIN蛋白7(NLP7)的直接调控。转录组分析鉴定出1038个受ERF56直接调控的候选基因。基因本体(GO)过度表达分析表明,ERF56参与水运输、无机分子跨膜运输、次生代谢物生物合成和细胞壁组织过程。我们揭示了ERF56通过调节无机分子跨膜运输、次生代谢物生物合成和细胞壁组织过程来抑制硝酸盐依赖的生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11fc/11765960/c0f34beffacc/ijms-26-00613-g001.jpg

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