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AtEDT1/HDG11 的激活表达通过上调茉莉酸生物合成促进拟南芥 edt1 突变体侧根的形成。

Activated expression of AtEDT1/HDG11 promotes lateral root formation in Arabidopsis mutant edt1 by upregulating jasmonate biosynthesis.

机构信息

School of Life Sciences, University of Science and Technology of China, Hefei 230027, China.

出版信息

J Integr Plant Biol. 2015 Dec;57(12):1017-30. doi: 10.1111/jipb.12347. Epub 2015 Jul 27.

DOI:10.1111/jipb.12347
PMID:25752924
Abstract

Root architecture is crucial for plants to absorb water and nutrients. We previously reported edt1 (edt1D) mutant with altered root architecture that contributes significantly to drought resistance. However, the underlying molecular mechanisms are not well understood. Here we report one of the mechanisms underlying EDT1/HDG11-conferred altered root architecture. Root transcriptome comparison between the wild type and edt1D revealed that the upregulated genes involved in jasmonate biosynthesis and signaling pathway were enriched in edt1D root, which were confirmed by quantitative RT-PCR. Further analysis showed that EDT1/HDG11, as a transcription factor, bound directly to the HD binding sites in the promoters of AOS, AOC3, OPR3, and OPCL1, which encode four key enzymes in JA biosynthesis. We found that the jasmonic acid level was significantly elevated in edt1D root compared with that in the wild type subsequently. In addition, more auxin accumulation was observed in the lateral root primordium of edt1D compared with that of wild type. Genetic analysis of edt1D opcl1 double mutant also showed that HDG11 was partially dependent on JA in regulating LR formation. Taken together, overexpression of EDT1/HDG11 increases JA level in the root of edt1D by directly upregulating the expressions of several genes encoding JA biosynthesis enzymes to activate auxin signaling and promote lateral root formation.

摘要

根系结构对于植物吸收水分和养分至关重要。我们之前曾报道过 edt1(edt1D)突变体,其根系结构发生改变,对干旱具有很强的抗性。然而,其潜在的分子机制尚不清楚。在这里,我们报告了 EDT1/HDG11 改变根系结构的潜在分子机制之一。野生型和 edt1D 之间的根系转录组比较表明,茉莉酸生物合成和信号通路中上调的基因在 edt1D 根中富集,这通过定量 RT-PCR 得到了证实。进一步的分析表明,EDT1/HDG11 作为一种转录因子,直接与 AOS、AOC3、OPR3 和 OPCL1 启动子中的 HD 结合位点结合,这些基因编码 JA 生物合成的四个关键酶。我们发现 edt1D 根中的茉莉酸水平明显高于野生型。此外,edt1D 侧根原基中积累的生长素也比野生型多。edt1D opcl1 双突变体的遗传分析也表明,HDG11 在调节侧根形成过程中部分依赖于 JA。综上所述,EDT1/HDG11 的过表达通过直接上调几个编码 JA 生物合成酶的基因的表达,增加 edt1D 根中的 JA 水平,激活生长素信号通路,促进侧根形成。

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