Abstract
Chemical genetics has emerged as a powerful approach to dissect biological processes, based on the utilization of small molecules disturbing the function of specific target proteins. By analogy with classical genetics, ‘reverse chemical genetics’ refers to the utilization of drugs acting on a known target, enabling its functional characterization at the levels of the cells, tissues and organisms. Likewise, ‘direct chemical genetics’ refers to the utilization of a drug of unknown mode of action, but triggering a phenotype of interest. In that case, one has to identify the target(s) possibly blocked (or possibly activated) by the small molecule. This chapter illustrates both approaches, like the analysis of the elongation of fatty acids, the biosynthesis of galactoglycerolipids or the catabolism of phosphoglycerolipids by reverse chemical genetics or the study of the membrane glycerolipid remodeling triggered upon phosphate starvation, by direct chemical genetics.
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Acknowledgements
All authors are supported by a grant from Agence Nationale de la Recherche (ANR Reglisse). EM is also supported by the ANR DiaDomOil grant, the OCEANOMICS program from the French Ministry of Research and the Institut Carnot LISA (Lipides pour la santé et l’industrie).
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Chevalier, F., Carrera, L.C., Nussaume, L., Maréchal, E. (2016). Chemical Genetics in Dissecting Membrane Glycerolipid Functions. In: Nakamura, Y., Li-Beisson, Y. (eds) Lipids in Plant and Algae Development. Subcellular Biochemistry, vol 86. Springer, Cham. https://doi.org/10.1007/978-3-319-25979-6_7
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DOI: https://doi.org/10.1007/978-3-319-25979-6_7
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