Schlüter Urte, Bräutigam Andrea, Gowik Udo, Melzer Michael, Christin Pascal-Antoine, Kurz Samantha, Mettler-Altmann Tabea, Weber Andreas Pm
Institute of Plant Biochemistry, Cluster of Excellence on Plant Sciences (CEPLAS), Heinrich Heine University, Universitätsstr. 1, 40225 Düsseldorf, Germany.
Network Analysis and Modelling, Leibniz Institute of Plant Genetics and Crop Research (IPK), OT Gatersleben, Corrensstr. 3, 06466 Stadt Seeland, Germany.
J Exp Bot. 2017 Jan;68(2):191-206. doi: 10.1093/jxb/erw391. Epub 2016 Oct 19.
Evolution of C photosynthesis is not distributed evenly in the plant kingdom. Particularly interesting is the situation in the Brassicaceae, because the family contains no C species, but several C-C intermediates, mainly in the genus Moricandia Investigation of leaf anatomy, gas exchange parameters, the metabolome, and the transcriptome of two C-C intermediate Moricandia species, M. arvensis and M. suffruticosa, and their close C relative M. moricandioides enabled us to unravel the specific C-C characteristics in these Moricandia lines. Reduced CO compensation points in these lines were accompanied by anatomical adjustments, such as centripetal concentration of organelles in the bundle sheath, and metabolic adjustments, such as the balancing of C and N metabolism between mesophyll and bundle sheath cells by multiple pathways. Evolution from C to C-C intermediacy was probably facilitated first by loss of one copy of the glycine decarboxylase P-protein, followed by dominant activity of a bundle sheath-specific element in its promoter. In contrast to recent models, installation of the C-C pathway was not accompanied by enhanced activity of the C cycle. Our results indicate that metabolic limitations connected to N metabolism or anatomical limitations connected to vein density could have constrained evolution of C in Moricandia.
C4光合作用的进化在植物界的分布并不均匀。十字花科的情况尤其有趣,因为该科没有C4物种,但有几种C3-C4中间类型,主要存在于辣根菜属。对两种C3-C4中间类型的辣根菜属植物——田野辣根菜和半灌木辣根菜,以及它们近缘的C3植物桑氏辣根菜的叶片解剖结构、气体交换参数、代谢组和转录组进行研究,使我们能够揭示这些辣根菜属植物品系中特定的C3-C4特征。这些品系中较低的CO2补偿点伴随着解剖结构的调整,如维管束鞘中细胞器向心集中,以及代谢调整,如通过多种途径平衡叶肉细胞和维管束鞘细胞之间的碳和氮代谢。从C3到C3-C4中间类型的进化可能首先是由于甘氨酸脱羧酶P蛋白的一个拷贝缺失,随后是其启动子中一个维管束鞘特异性元件的显性活性。与最近的模型不同,C3-C4途径的建立并没有伴随着C3循环活性的增强。我们的结果表明,与氮代谢相关的代谢限制或与叶脉密度相关的解剖限制可能限制了辣根菜属植物中C4的进化。