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ZmEREB25转录因子通过与ZmARF27相互作用介导玉米胚乳中核心淀粉合成基因的反式激活。

ZmEREB25 transcription factor mediates transactivation of core starch synthetic genes in maize endosperm via interaction with ZmARF27.

作者信息

Wang Yayun, Long Tiandan, Hu Xiyue, Qin Aying, Zhang Ruonan, Gao Lei, Fan Xiujun, Hu Yufeng, Wang Mei, Huang Yubi, Li Yangping

机构信息

State Key Laboratory of Crop Gene Resource Exploration and Utilization in Southwest China, Sichuan Agricultural University, Chengdu, 611130, China.

State Key Laboratory of Crop Gene Resource Exploration and Utilization in Southwest China, Sichuan Agricultural University, Chengdu, 611130, China; Sichuan Neijiang Academy of Agricultural Sciences, Neijiang, 641000, China.

出版信息

Plant Physiol Biochem. 2025 Feb;219:109360. doi: 10.1016/j.plaphy.2024.109360. Epub 2024 Nov 28.

Abstract

Starch, as the primary storage material in maize endosperm, is essential in determining yield and quality. Although the starch biosynthetic pathway in maize has been well-documented, the transcriptional network underlying endosperm starch synthesis remains elusive. Through a comprehensive co-expression analysis, we screened an endosperm-preferential AP2/ERF transcription factor ZmEREB25, which exhibited a strong correlation with the expression pattern of starch biosynthetic genes in maize endosperm. ZmEREB25 enhanced the promoter activities of the core starch biosynthetic genes, namely Sh2, SSIIIa and SSI, through specific binding to the GCCGAC-containing elements present in their promoters. Given that ZmEREB25 lacked the transactivation capacity, we further identified an ARF transcription factor, ZmARF27, that interacted with ZmEREB25 to coordinately transactivate the promoters of Sh2, SSIIIa and SSI genes via direct binding to these promoters. Our present study demonstrated that the ZmEREB25-ZmARF27 complex is crucial for transactivating core starch synthetic genes in maize endosperm and uncovered a novel regulatory pathway for starch synthesis in maize endosperm.

摘要

淀粉作为玉米胚乳中的主要储存物质,对于决定产量和品质至关重要。尽管玉米中的淀粉生物合成途径已有充分记载,但胚乳淀粉合成的转录调控网络仍不清楚。通过全面的共表达分析,我们筛选出了一个胚乳优先表达的AP2/ERF转录因子ZmEREB25,它与玉米胚乳中淀粉生物合成基因的表达模式具有很强的相关性。ZmEREB25通过特异性结合其启动子中含GCCGAC的元件,增强了核心淀粉生物合成基因Sh2、SSIIIa和SSI的启动子活性。鉴于ZmEREB25缺乏反式激活能力,我们进一步鉴定了一个ARF转录因子ZmARF27,它与ZmEREB25相互作用,通过直接结合这些启动子来协同反式激活Sh2、SSIIIa和SSI基因的启动子。我们目前的研究表明,ZmEREB25-ZmARF27复合物对于反式激活玉米胚乳中的核心淀粉合成基因至关重要,并揭示了玉米胚乳淀粉合成的一条新的调控途径。

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