MdERF1B-miR482c-MdCCR4-MdTLP1b模块调控苹果对炭疽病的抗性。

IF 9.5 Q1 GENETICS & HEREDITY
园艺研究(英文) Pub Date : 2026-05-21 eCollection Date: 2026-10-01 DOI:10.1093/hr/uhag199
Baodong Zhang, Jialin Cong, Zongshan Zhou
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引用次数: 0

摘要

由炭疽病菌(Colletotrichum gloeosporioides)引起的肾小球叶斑病(Glomerella leaf spot, GLS)对苹果(Malus domestica)的生产构成了严重威胁。microRNAs (miRNAs)是植物-病原体串扰的关键调控因子。然而,miR482调控苹果对GLS抗性的潜在机制尚不清楚。在这里,我们发现miR482c的过表达降低了对gloeosporioides的抗性,而沉默miR482c则赋予了对gloeosporioides的抗性。苹果的5'RACE实验和本烟的共表达实验证实,miR482c靶向并切割MdCCR4 mRNA。随后的研究发现,MdCCR4过表达可显著增强苹果对gloeosporioides的抗性。值得注意的是,MdCCR4与thumatin样蛋白MdTLP1b物理相互作用,MdTLP1b也正调控对gloeosporioides的抗性。此外,通过生物信息学和Y1H筛选,MdERF1B被鉴定为miR482c的上游调控因子,并进一步证实MdERF1B通过直接结合其启动子负调控miR482c的转录。与此同时,MdERF1B过表达增强了对gloeosporioides的抗性,而沉默MdERF1B则降低了对gloeosporioides的抗性。综上所述,我们的研究结果表明,MdERF1B-miR482c-MdCCR4-MdTLP1b调控网络在苹果抵御gloeosporioides的过程中起着关键作用,突出了抗病基因改良的有希望的候选基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The MdERF1B-miR482c-MdCCR4-MdTLP1b module regulates apple resistance to Colletotrichum gloeosporioides.

Glomerella leaf spot (GLS), incited by Colletotrichum gloeosporioides, poses a significant threat to apple (Malus domestica) production. microRNAs (miRNAs) are critical regulators of plant-pathogen crosstalk. However, the underlying mechanism through which miR482 regulates apple resistance to GLS remains unclear. Here, we show that overexpression of miR482c compromises resistance against C. gloeosporioides, while silencing miR482c confers resistance to C. gloeosporioides. 5'RACE assays in apple and co-expression assays in Nicotiana benthamiana confirmed that miR482c targets and cleaves the MdCCR4 mRNA. Subsequent research revealed that overexpression of MdCCR4 significantly enhances apple resistance to C. gloeosporioides. Notably, MdCCR4 physically interacts with the thaumatin-like protein MdTLP1b, which also positively regulates resistance to C. gloeosporioides. Additionally, MdERF1B was identified as an upstream regulator of miR482c through bioinformatics and Y1H screening, and was further confirmed to negatively regulate miR482c transcription by directly binding to its promoter. Meanwhile, MdERF1B overexpression enhances resistance to C. gloeosporioides, while silencing MdERF1B compromises resistance to C. gloeosporioides. Collectively, our findings indicate that the MdERF1B-miR482c-MdCCR4-MdTLP1b regulatory network is pivotal for apple defense against C. gloeosporioides, highlighting promising candidates for the genetic improvement of disease resistance.

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CiteScore
12.90
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