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茉莉酸激活的转录因子MdMYC2在苹果果实成熟过程中调控乙烯生物合成基因以促进乙烯生物合成。

The Jasmonate-Activated Transcription Factor MdMYC2 Regulates and Ethylene Biosynthetic Genes to Promote Ethylene Biosynthesis during Apple Fruit Ripening.

作者信息

Li Tong, Xu Yaxiu, Zhang Lichao, Ji Yinglin, Tan Dongmei, Yuan Hui, Wang Aide

机构信息

College of Horticulture, Shenyang Agricultural University, Shenyang 110866, China.

College of Horticulture, Shenyang Agricultural University, Shenyang 110866, China

出版信息

Plant Cell. 2017 Jun;29(6):1316-1334. doi: 10.1105/tpc.17.00349. Epub 2017 May 26.

Abstract

The plant hormone ethylene is critical for ripening in climacteric fruits, including apple (). Jasmonate (JA) promotes ethylene biosynthesis in apple fruit, but the underlying molecular mechanism is unclear. Here, we found that JA-induced ethylene production in apple fruit is dependent on the expression of , an ACC synthase gene involved in ethylene biosynthesis. The expression of , encoding a transcription factor involved in the JA signaling pathway, was enhanced by MeJA treatment in apple fruits, and MdMYC2 directly bound to the promoters of both and the ACC oxidase gene and enhanced their transcription. Furthermore, MdMYC2 bound to the promoter of , encoding a transcription factor involved in the ethylene-signaling pathway, thereby activating transcription. We also found that MdMYC2 interacted with MdERF2, a suppressor of and This protein interaction prevented MdERF2 from interacting with MdERF3 and from binding to the promoter, leading to increased transcription of Collectively, these results indicate that JA promotes ethylene biosynthesis through the regulation of MdERFs and ethylene biosynthetic genes by MdMYC2.

摘要

植物激素乙烯对于跃变型果实(包括苹果)的成熟至关重要。茉莉酸(JA)促进苹果果实中的乙烯生物合成,但其潜在的分子机制尚不清楚。在这里,我们发现JA诱导苹果果实中乙烯的产生依赖于MdACS1,这是一个参与乙烯生物合成的ACC合酶基因的表达。MdMYC2的表达,编码一个参与JA信号通路的转录因子,在苹果果实中通过茉莉酸甲酯(MeJA)处理得到增强,并且MdMYC2直接结合到MdACS1和ACC氧化酶基因MdACO1的启动子上并增强它们的转录。此外,MdMYC2结合到MdEIL1的启动子上,MdEIL1编码一个参与乙烯信号通路的转录因子,从而激活MdEIL1转录。我们还发现MdMYC2与MdERF2相互作用,MdERF2是MdEIL1和MdACS1的一个抑制因子。这种蛋白质相互作用阻止MdERF2与MdERF3相互作用以及与MdACS1启动子结合,导致MdACS1转录增加。总的来说,这些结果表明JA通过MdMYC2对MdERFs和乙烯生物合成基因的调控促进乙烯生物合成。

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