Hello darkness, my old friend: 3-KETOACYL-COENZYME A SYNTHASE4 is a branch point in the regulation of triacylglycerol synthesis in Arabidopsis thaliana

Abstract Plant lipids are important as alternative sources of carbon and energy when sugars or starch are limited. Here, we applied combined heat and darkness or extended darkness to a panel of ∼300 Arabidopsis (Arabidopsis thaliana) accessions to study lipid remodeling under carbon starvation. Natu...

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Published inThe Plant cell Vol. 35; no. 6; pp. 1984 - 2005
Main Authors Luzarowska, Urszula, Ruß, Anne-Kathrin, Joubès, Jérôme, Batsale, Marguerite, Szymański, Jędrzej, P. Thirumalaikumar, Venkatesh, Luzarowski, Marcin, Wu, Si, Zhu, Feng, Endres, Niklas, Khedhayir, Sarah, Schumacher, Julia, Jasinska, Weronika, Xu, Ke, Correa Cordoba, Sandra Marcela, Weil, Simy, Skirycz, Aleksandra, Fernie, Alisdair Robert, Li-Beisson, Yonghua, Fusari, Corina M, Brotman, Yariv
Format Journal Article
LanguageEnglish
Published US Oxford University Press 29.05.2023
American Society of Plant Biologists (ASPB)
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Summary:Abstract Plant lipids are important as alternative sources of carbon and energy when sugars or starch are limited. Here, we applied combined heat and darkness or extended darkness to a panel of ∼300 Arabidopsis (Arabidopsis thaliana) accessions to study lipid remodeling under carbon starvation. Natural allelic variation at 3-KETOACYL-COENZYME A SYNTHASE4 (KCS4), a gene encoding an enzyme involved in very long chain fatty acid (VLCFA) synthesis, underlies the differential accumulation of polyunsaturated triacylglycerols (puTAGs) under stress. Ectopic expression of KCS4 in yeast and plants proved that KCS4 is a functional enzyme localized in the endoplasmic reticulum with specificity for C22 and C24 saturated acyl-CoA. Allelic mutants and transient overexpression in planta revealed the differential role of KCS4 alleles in VLCFA synthesis and leaf wax coverage, puTAG accumulation, and biomass. Moreover, the region harboring KCS4 is under high selective pressure and allelic variation at KCS4 correlates with environmental parameters from the locales of Arabidopsis accessions. Our results provide evidence that KCS4 plays a decisive role in the subsequent fate of fatty acids released from chloroplast membrane lipids under carbon starvation. This work sheds light on both plant response mechanisms and the evolutionary events shaping the lipidome under carbon starvation. Natural variation at KCS4 underlies a differential accumulation of polyunsaturated triacylglycerols under carbon starvation, by acting as a branch point in the fate of fatty acids.
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Corina M. Fusari and Yariv Brotman senior authors.
The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (https://academic.oup.com/plcell) is: Corina M. Fusari and Yariv Brotman.
Conflict of interest statement. None declared.
ISSN:1040-4651
1532-298X
DOI:10.1093/plcell/koad059