Functional Overlap of Long-Chain Acyl-CoA Synthetases in Arabidopsis.

Long-chain acyl-CoA synthetases (LACSs) play diverse and essential roles in lipid metabolism. The genomes of model eukaryotic organisms encode multiple LACS genes, and the substrate specificities of LACS homologs often overlap substantially. Homologous LACSs tend to differ in their expression patterns, localizations, and, by extension, the metabolic pathways to which they contribute. The Arabidopsis genome encodes a family of nine LACS genes, which have been characterized largely by reverse genetic analysis of mutant phenotypes. Because of redundancy, distinguishing the contributions of some Arabidopsis LACS genes has been challenging. Here, we have attempted to clarify the functions of LACSs that functionally overlap by synopsizing the results of previous work, isolating a suite of higher-order mutants that were previously lacking, and analyzing oil, wax, cutin, cuticle permeability, fertility and growth phenotypes. LACS1, LACS2, LACS4, LACS8 and LACS9 all affect cuticular lipid metabolism, but have different precise roles. Seed set, seed weight and storage oil amounts of higher-order lacs1, lacs2, lacs4, lacs8 and lacs9 mutants vary greatly, with these traits subject to different effects of fertility and oil synthesis defects. LACS4, LACS8 and LACS9 have partially redundant roles in development, as lacs4 lacs8 and lacs4 lacs9 double mutants are dwarf. lacs4 lacs8 lacs9 triple mutants were not recovered, and are assumed to be non-viable. Together, these results sketch a complex network of functions and functional interactions within the Arabidopsis LACS gene family.

Zhao L ，Haslam TM ，Sonntag A ，Molina I ，Kunst L ... -  《-》

Insertional mutant analysis reveals that long-chain acyl-CoA synthetase 1 (LACS1), but not LACS8, functionally overlaps with LACS9 in Arabidopsis seed oil biosynthesis.

Triacylglycerols (TAGs) are major storage materials that accumulate in developing seeds and serve as carbon and energy reserves for germination and growth of the seedling. One of the critical reactions in TAG biosynthesis is activation of fatty acyl chains to fatty acyl CoAs, catalyzed by long-chain acyl CoA synthetases (LACSs). Of the nine LACSs identified in Arabidopsis, only LACS9 is known to reside in the plastid, the site of de novo fatty acid synthesis, and is considered the major LACS isoform involved in plastidial fatty acid export for TAG formation. Because the lacs9 null mutant did not show any detectable phenotype, it was hypothesized that at least one additional LACS enzyme must be active in the plastid. Expression analyses to identify potential plastid-localized LACSs involved in TAG biosynthesis revealed that, in addition to LACS9, isoforms LACS1, LACS2, LACS4 and LACS8 are transcribed in the seed. LACS8 showed the highest expression level in the embryo and a high sequence similarity with LACS9, and was therefore characterized further and shown to be associated with the ER, not the plastid. Furthermore, disruption of LACS8 in the lacs8 mutant and lacs8 lacs9 double mutant, and over-expression of LACS8, did not affect the seed fatty acid content. In contrast, 11 and 12% decreases in fatty acid content were detected in lacs1 lacs9 and lacs1 lacs8 lacs9 seeds, respectively, indicating that LACS1 and LACS9 have overlapping functions in TAG biosynthesis. This result is surprising because, unlike LACS9, LACS1 is localized in the ER and has been shown to be involved in cuticular lipid synthesis.

Zhao L ，Katavic V ，Li F ，Haughn GW ，Kunst L ... -  《-》

Organ fusion and defective cuticle function in a lacs1 lacs2 double mutant of Arabidopsis.

Weng H ，Molina I ，Shockey J ，Browse J ... -  《-》

Arabidopsis CER8 encodes LONG-CHAIN ACYL-COA SYNTHETASE 1 (LACS1) that has overlapping functions with LACS2 in plant wax and cutin synthesis.

Lü S ，Song T ，Kosma DK ，Parsons EP ，Rowland O ，Jenks MA ... -  《-》

Two activities of long-chain acyl-coenzyme A synthetase are involved in lipid trafficking between the endoplasmic reticulum and the plastid in Arabidopsis.

In plants, fatty acids are synthesized within the plastid and need to be distributed to the different sites of lipid biosynthesis within the cell. Free fatty acids released from the plastid need to be converted to their corresponding coenzyme A thioesters to become metabolically available. This activation is mediated by long-chain acyl-coenzyme A synthetases (LACSs), which are encoded by a family of nine genes in Arabidopsis (Arabidopsis thaliana). So far, it has remained unclear which of the individual LACS activities are involved in making plastid-derived fatty acids available to cytoplasmic glycerolipid biosynthesis. Because of its unique localization at the outer envelope of plastids, LACS9 was regarded as a candidate for linking plastidial fatty export and cytoplasmic use. However, data presented in this study show that LACS9 is involved in fatty acid import into the plastid. The analyses of mutant lines revealed strongly overlapping functions of LACS4 and LACS9 in lipid trafficking from the endoplasmic reticulum to the plastid. In vivo labeling experiments with lacs4 lacs9 double mutants suggest strongly reduced synthesis of endoplasmic reticulum-derived lipid precursors, which are required for the biosynthesis of glycolipids in the plastids. In conjunction with this defect, double-mutant plants accumulate significant amounts of linoleic acid in leaf tissue.

Jessen D ，Roth C ，Wiermer M ，Fulda M ... -  《-》