Characterization of maize leaf pyruvate orthophosphate dikinase using high throughput sequencing

被引:12
作者
Zhang, Yuling [1 ]
Giuliani, Rita [2 ]
Zhang, Youjun [3 ]
Zhang, Yang [4 ]
Araujo, Wagner Luiz [3 ]
Wang, Baichen [5 ]
Liu, Peng [6 ]
Sun, Qi [7 ]
Cousins, Asaph [2 ]
Edwards, Gerald [2 ]
Fernie, Alisdair [3 ]
Brutnell, Thomas P. [8 ]
Li, Pinghua [1 ]
机构
[1] Shandong Agr Univ, Coll Agron Sci, State Key Lab Crop Biol, Tai An 271018, Shandong, Peoples R China
[2] Washington State Univ, Sch Biol Sci, Mol Plant Sci, Pullman, WA 99164 USA
[3] Max Planck Inst Mol Pflanzenphysiol, Muhlenberg 1, D-14476 Potsdam, Germany
[4] Univ Nebraska, Dept Agron & Hort, Lincoln, NE 68583 USA
[5] Chinese Acad Sci, Inst Bot, Photosynthesis Res Ctr, Key Lab Photobiol, 20 Nanxincun, Beijing 100093, Peoples R China
[6] Iowa State Univ, Dept Stat, Ames, IA 50011 USA
[7] Cornell Univ, Life Sci Core Labs Ctr, Computat Biol Serv Unit, Ithaca, NY 14850 USA
[8] Donald Danforth Plant Sci Ctr, St Louis, MO 63132 USA
关键词
NADP-MALATE DEHYDROGENASE; BUNDLE-SHEATH-CELLS; C-4; PHOTOSYNTHESIS; PYRUVATE; ORTHOPHOSPHATE DIKINASE; DIFFERENTIAL EXPRESSION; NITROGEN REMOBILIZATION; GAS-CHROMATOGRAPHY; GLOBAL FOOD; ZEA-MAYS; ARABIDOPSIS;
D O I
10.1111/jipb.12656
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In C-4 photosynthesis, pyruvate orthophosphate dikinase (PPDK) catalyzes the regeneration of phosphoenolpyruvate in the carbon shuttle pathway. Although the biochemical function of PPDK in maize is well characterized, a genetic analysis of PPDK has not been reported. In this study, we use the maize transposable elements Mutator and Ds to generate multiple mutant alleles of PPDK. Loss-of-function mutants are seedling lethal, even when plants were grown under 2% CO2, and they show very low capacity for CO2 assimilation, indicating C-4 photosynthesis is essential in maize. Using RNA-seq and GC-MS technologies, we examined the transcriptional and metabolic responses to a deficiency in PPDK activity. These results indicate loss of PPDK results in downregulation of gene expression of enzymes of the C-4 cycle, the Calvin cycle, and components of photochemistry. Furthermore, the loss of PPDK did not change Kranz anatomy, indicating that this metabolic defect in the C-4 cycle did not impinge on the morphological differentiation of C-4 characters. However, sugar metabolism and nitrogen utilization were altered in the mutants. An interaction between light intensity and genotype was also detected from transcriptome profiling, suggesting altered transcriptional and metabolic responses to environmental and endogenous signals in the PPDK mutants.
引用
收藏
页码:670 / 690
页数:21
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