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亚麻 LuWRKY36 的鉴定,作为一种转录因子,其能响应亚麻发根中的尖孢镰刀菌诱导子促进次生亚麻醇的生物合成。

Characterization of LuWRKY36, a flax transcription factor promoting secoisolariciresinol biosynthesis in response to Fusarium oxysporum elicitors in Linum usitatissimum L. hairy roots.

机构信息

Laboratoire de Biologie des Ligneux et des Grandes Cultures, EA 1207, INRA USC 1328, Université d'Orléans, Pôle Universitaire d'Eure et Loir, 21 Rue de Loigny la Bataille, 28000, Chartres, France.

出版信息

Planta. 2019 Jul;250(1):347-366. doi: 10.1007/s00425-019-03172-9. Epub 2019 Apr 29.

DOI:10.1007/s00425-019-03172-9
PMID:31037486
Abstract

The involvement of a WRKY transcription factor in the regulation of lignan biosynthesis in flax using a hairy root system is described. Secoisolariciresinol is the main flax lignan synthesized by action of LuPLR1 (pinoresinol-lariciresinol reductase 1). LuPLR1 gene promoter deletion experiments have revealed a promoter region containing W boxes potentially responsible for the response to Fusarium oxysporum. W boxes are bound by WRKY transcription factors that play a role in the response to stress. A candidate WRKY transcription factor, LuWRKY36, was isolated from both abscisic acid and Fusarium elicitor-treated flax cell cDNA libraries. This transcription factors contains two WRKY DNA-binding domains and is a homolog of AtWRKY33. Different approaches confirmed LuWRKY36 binding to a W box located in the LuPLR1 promoter occurring through a unique direct interaction mediated by its N-terminal WRKY domain. Our results propose that the positive regulator action of LuWRKY36 on the LuPLR1 gene regulation and lignan biosynthesis in response to biotic stress is positively mediated by abscisic acid and inhibited by ethylene. Additionally, we demonstrate a differential Fusarium elicitor response in susceptible and resistant flax cultivars, seen as a faster and stronger LuPLR1 gene expression response accompanied with higher secoisolariciresinol accumulation in HR of the resistant cultivar.

摘要

描述了利用发根系统中 WRKY 转录因子参与调控亚麻木质素生物合成的机制。亚麻木脂素是由 LuPLR1(松脂醇-落叶松脂素还原酶 1)作用合成的主要亚麻木质素。LuPLR1 基因启动子缺失实验揭示了一个含有 W 盒的启动子区域,该区域可能负责对尖孢镰刀菌的响应。W 盒由 WRKY 转录因子结合,WRKY 转录因子在应激响应中发挥作用。从脱落酸和尖孢镰刀菌诱导处理的亚麻细胞 cDNA 文库中分离出一个候选 WRKY 转录因子 LuWRKY36。该转录因子包含两个 WRKY DNA 结合域,是 AtWRKY33 的同源物。不同的方法证实了 LuWRKY36 与位于 LuPLR1 启动子中的 W 盒结合,这种结合是通过其 N 端 WRKY 结构域介导的独特直接相互作用发生的。我们的研究结果表明,LuWRKY36 对 LuPLR1 基因调控和木质素生物合成的正调控作用是通过脱落酸正向介导的,而乙烯抑制这种作用。此外,我们还证明了在易感和抗性亚麻品种中尖孢镰刀菌诱导存在差异,表现为抗性品种 HR 中 LuPLR1 基因表达更快、更强,同时伴随着更高水平的亚麻木脂素积累。

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2
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Planta. 2019 Jun;249(6):1695-1714. doi: 10.1007/s00425-019-03137-y. Epub 2019 Mar 20.
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