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Identifying Essential Genes/reactions of the Rice Photorespiration by in Silico Model-based Analysis

Overview
Journal Rice (N Y)
Date 2013 Nov 28
PMID 24280628
Citations 8
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Abstract

Background: Photorespiration, a highly wasteful process of energy dissipation, depresses the productivity of C3 plants such as rice (Oryza sativa) under dry and hot conditions. Thus, it is highly required to understand the cellular physiology and relevant metabolic states under photorespiration using systems approaches, thereby devising strategies for improving rice production.

Findings: In silico model-driven gene deletion analysis was performed on photorespiring leaf cells under ambient and stressed environmental conditions using our central metabolic network of rice cells. As a result, we identified a number of essential genes for the cell growth across various functional pathways such as photorespiratory cycle, Calvin cycle, GS-GOGAT cycle and sucrose metabolism as well as certain inter-compartmental transporters, which are mostly in good agreement with previous experiments. Synthetic lethal (SL) screening was also performed to identify the pair of non-essential genes whose simultaneous deletion become lethal, revealing the existence of more than 220 pairs of SLs on rice central metabolism.

Conclusions: The gene deletion and synthetic lethal analyses highlighted the rigid nature of rice photosynthetic pathways and characterized functional interactions between central metabolic genes, respectively. The biological roles of such reported essential genes should be further explored to better understand the rice photorespiration in future.

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References
1.
Pick T, Brautigam A, Schulz M, Obata T, Fernie A, Weber A . PLGG1, a plastidic glycolate glycerate transporter, is required for photorespiration and defines a unique class of metabolite transporters. Proc Natl Acad Sci U S A. 2013; 110(8):3185-90. PMC: 3581909. DOI: 10.1073/pnas.1215142110. View

2.
Suthers P, Zomorrodi A, Maranas C . Genome-scale gene/reaction essentiality and synthetic lethality analysis. Mol Syst Biol. 2009; 5:301. PMC: 2736653. DOI: 10.1038/msb.2009.56. View

3.
Zelitch I, Schultes N, Peterson R, Brown P, Brutnell T . High glycolate oxidase activity is required for survival of maize in normal air. Plant Physiol. 2008; 149(1):195-204. PMC: 2613714. DOI: 10.1104/pp.108.128439. View

4.
Wingler A, Lea P, Quick W, Leegood R . Photorespiration: metabolic pathways and their role in stress protection. Philos Trans R Soc Lond B Biol Sci. 2000; 355(1402):1517-29. PMC: 1692872. DOI: 10.1098/rstb.2000.0712. View

5.
Voll L, Jamai A, Renne P, Voll H, McClung C, Weber A . The photorespiratory Arabidopsis shm1 mutant is deficient in SHM1. Plant Physiol. 2005; 140(1):59-66. PMC: 1326031. DOI: 10.1104/pp.105.071399. View