Splice-site variant in ACSL5: a marker promoting opposing effect on cell viability and protein expression

• Published in: European journal of human genetics : EJHG Vol. 27; no. 12; pp. 1836 - 1844
• Main Authors: Pérez-Núñez, Iván, Karaky, Mohamad, Fedetz, María, Barrionuevo, Cristina, Izquierdo, Guillermo, Matesanz, Fuencisla, Alcina, Antonio
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 01-12-2019; Springer International Publishing
• Subjects: 12-O-Tetradecanoylphorbol-13-acetate; Acetic acid; Astrocytoma - genetics; Astrocytoma - pathology; Carcinogenesis; Cell culture; Cell Survival - genetics; Cell viability; Coenzyme A; Coenzyme A - genetics; Coenzyme A Ligases - genetics; Exons - genetics; Fatty acids; Genomes; Genotypes; HEK293 Cells; Human Genome Project; Humans; Ionomycin; Lipid metabolism; Lipid Metabolism - genetics; Lymphoblastoid cell lines; Metabolic Diseases - genetics; Metabolic Diseases - pathology; Metabolic disorders; Neoplasms - genetics; Neoplasms - pathology; Oligodendroglia - pathology; Protein expression; Protein Isoforms - genetics; Proteins; Reactive oxygen species; Ribonucleic acid; RNA; RNA Splicing - genetics; Transfection
• ISSN: 1018-4813; 1476-5438
• DOI: 10.1038/s41431-019-0414-5

Long-chain Acyl-CoA synthetases (ACSLs) activate fatty acids (FAs) by thioesterification with Coenzyme A (CoA), generating FA-CoAs. These products are essential for lipid metabolism and carcinogenesis. In previous study, we identified an intronic variant rs2256368:A>G, whose G allele promotes exon 20 skipping in up to 43% of ACSL5 transcripts but its functional relevance is unclear. Here, we compared the expression of splice (Spl) and nonsplice (NSpl) ACSL5 variants and the effect on cell viability under culture conditions that force cells to metabolize fatty acids. We found that lymphoblastoid cell lines from 1000 Genomes Project, bearing Spl genotypes, showed a reduced expression of total ACSL5 protein due to an inefficient translation of the Spl RNA. These cells impaired growth in cultures with phorbol myristate acetate-ionomycin (PMA-Io) or medium deprived of glucose, while production of reactive oxygen species increased in PMA-Io. Specific ACSL5-isoform transfection in HEK239T (kidney), U87 (astroglioma), and HOG (oligodendrocyte) cells showed the Spl protein to be the causal factor of cell-growth inhibition, despite its reduced protein expression. Our findings indicate that the variant rs2256368:A>G can predict a growth inhibitory activity, caused by the Spl isoform of ACSL5 protein, opposed to the activity of the NSpl. Deep understanding of its functioning might have application in metabolic diseases and cancer.