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Nudix 水解酶基因家族的功能多样化驱动了野蔷薇属杂种香水月季中倍半萜生物合成。

Functional diversification in the Nudix hydrolase gene family drives sesquiterpene biosynthesis in Rosa × wichurana.

机构信息

Univ Lyon, UJM-Saint-Etienne, CNRS, BVpam FRE 3727, Saint-Etienne, F-42023, France.

Green Life Sciences Research Cluster, Swammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, Amsterdam, 1098 XH, The Netherlands.

出版信息

Plant J. 2020 Sep;104(1):185-199. doi: 10.1111/tpj.14916. Epub 2020 Jul 22.

Abstract

Roses use a non-canonical pathway involving a Nudix hydrolase, RhNUDX1, to synthesize their monoterpenes, especially geraniol. Here we report the characterization of another expressed NUDX1 gene from the rose cultivar Rosa x wichurana, RwNUDX1-2. In order to study the function of the RwNUDX1-2 protein, we analyzed the volatile profiles of an F progeny generated by crossing R. chinensis cv. 'Old Blush' with R. x wichurana. A correlation test of the volatilomes with gene expression data revealed that RwNUDX1-2 is involved in the biosynthesis of a group of sesquiterpenoids, especially E,E-farnesol, in addition to other sesquiterpenes. In vitro enzyme assays and heterologous in planta functional characterization of the RwNUDX1-2 gene corroborated this result. A quantitative trait locus (QTL) analysis was performed using the data of E,E-farnesol contents in the progeny and a genetic map was constructed based on gene markers. The RwNUDX1-2 gene co-localized with the QTL for E,E-farnesol content, thereby confirming its function in sesquiterpenoid biosynthesis in R. x wichurana. Finally, in order to understand the structural bases for the substrate specificity of rose NUDX proteins, the RhNUDX1 protein was crystallized, and its structure was refined to 1.7 Å. By molecular modeling of different rose NUDX1 protein complexes with their respective substrates, a structural basis for substrate discrimination by rose NUDX1 proteins is proposed.

摘要

玫瑰利用一种非经典途径,涉及一种 Nudix 水解酶 RhNUDX1,来合成其单萜,特别是香叶醇。在这里,我们报道了另一种来自玫瑰品种 Rosa x wichurana 的表达 NUDX1 基因,RwNUDX1-2。为了研究 RwNUDX1-2 蛋白的功能,我们分析了通过杂交 R. chinensis cv. 'Old Blush' 和 R. x wichurana 产生的 F 后代的挥发性图谱。挥发物图谱与基因表达数据的相关测试表明,RwNUDX1-2 除了其他倍半萜外,还参与一组倍半萜,特别是 E,E-法呢醇的生物合成。体外酶测定和 RwNUDX1-2 基因的异源植物功能鉴定证实了这一结果。使用后代中 E,E-法呢醇含量的数据进行了数量性状位点 (QTL) 分析,并基于基因标记构建了遗传图谱。RwNUDX1-2 基因与 E,E-法呢醇含量的 QTL 共定位,从而证实了其在 R. x wichurana 中倍半萜生物合成中的功能。最后,为了了解玫瑰 NUDX 蛋白底物特异性的结构基础,我们对 RhNUDX1 蛋白进行了结晶,并将其结构精修至 1.7 Å。通过不同玫瑰 NUDX1 蛋白与各自底物的复合物的分子建模,提出了玫瑰 NUDX1 蛋白对底物进行区分的结构基础。

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