Fernández-Escalada Manuel, Zulet-González Ainhoa, Gil-Monreal Miriam, Zabalza Ana, Ravet Karl, Gaines Todd, Royuela Mercedes
Departamento Ciencias del Medio Natural, Universidad Pública de Navarra, Pamplona, Spain.
Department of Bioagricultural Sciences and Pest Management, Colorado State University, Fort Collins, CO, United States.
Front Plant Sci. 2017 Nov 16;8:1970. doi: 10.3389/fpls.2017.01970. eCollection 2017.
A key enzyme of the shikimate pathway, 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS; EC 2.5.1.19), is the known target of the widely used herbicide glyphosate. Glyphosate resistance in , one of the most troublesome weeds in agriculture, has evolved through increased gene copy number. The aim of this work was to study the pleiotropic effects of () increased transcript abundance due to gene copy number variation (CNV) and of () glyphosate application on the aromatic amino acid (AAA) and branched chain amino acid (BCAA) synthesis pathways. Hydroponically grown glyphosate sensitive (GS) and glyphosate resistant (GR) plants were treated with glyphosate 3 days after treatment. In absence of glyphosate treatment, high gene copy number had only a subtle effect on transcriptional regulation of AAA and BCAA pathway genes. In contrast, glyphosate treatment provoked a general accumulation of the transcripts corresponding to genes of the AAA pathway leading to synthesis of chorismate in both GS and GR. After chorismate, anthranilate synthase transcript abundance was higher while chorismate mutase transcription showed a small decrease in GR and remained stable in GS, suggesting a regulatory branch point in the pathway that favors synthesis toward tryptophan over phenylalanine and tyrosine after glyphosate treatment. This was confirmed by studying enzyme activities and amino acid analysis. Importantly, this upregulation was glyphosate dose dependent and was observed similarly in both GS and GR populations. Glyphosate treatment also had a slight effect on the expression of BCAA genes but no general effect on the pathway could be observed. Taken together, our observations suggest that the high CNV of in GR populations has no major pleiotropic effect on the expression of AAA biosynthetic genes, even in response to glyphosate treatment. This finding supports the idea that the fitness cost associated with CNV in may be limited.
莽草酸途径的关键酶——5-烯醇丙酮酰莽草酸-3-磷酸合酶(EPSPS;EC 2.5.1.19),是广泛使用的除草剂草甘膦的已知作用靶点。农业中最棘手的杂草之一—— ,其对草甘膦的抗性是通过增加 基因拷贝数进化而来的。本研究的目的是探讨()由于基因拷贝数变异(CNV)导致的 转录丰度增加以及()草甘膦处理对芳香族氨基酸(AAA)和支链氨基酸(BCAA)合成途径的多效性影响。水培生长的草甘膦敏感(GS)和草甘膦抗性(GR)植株在处理3天后用草甘膦处理。在未进行草甘膦处理时,高 基因拷贝数对AAA和BCAA途径基因的转录调控仅有细微影响。相比之下,草甘膦处理引发了AAA途径中与基因相对应的转录本普遍积累,导致GS和GR中分支酸的合成均增加了。在分支酸之后,邻氨基苯甲酸合酶的转录丰度更高,而分支酸变位酶的转录在GR中略有下降,在GS中保持稳定,这表明在草甘膦处理后,该途径中存在一个调控分支点,有利于向色氨酸而非苯丙氨酸和酪氨酸的合成方向进行。通过研究酶活性和氨基酸分析证实了这一点。重要的是,这种上调是草甘膦剂量依赖性的,并在GS和GR群体中均有类似观察结果。草甘膦处理对BCAA基因的表达也有轻微影响,但未观察到对该途径有普遍影响。综上所述,我们的观察结果表明,即使在草甘膦处理后,GR群体中 的高CNV对AAA生物合成基因的表达也没有主要的多效性影响。这一发现支持了与 中CNV相关的适合度代价可能有限的观点。