Regulation of the CoA Biosynthetic Complex Assembly in Mammalian Cells

• Published in: International journal of molecular sciences 2021-01, Vol.22 (3), p.1131
• Main Authors: Baković, Jovana, López Martínez, David, Nikolaou, Savvas, Yu, Bess Yi Kun, Tossounian, Maria-Armineh, Tsuchiya, Yugo, Thrasivoulou, Christopher, Filonenko, Valeriy, Gout, Ivan
• Format: Article
• Language: English
• Subjects: A549 Cells; Antioxidants; Biosynthesis; Biosynthetic Pathways - genetics; Cellular stress response; Coenzyme A; Coenzyme A - biosynthesis; Coenzyme A - metabolism; Diabetes mellitus; Enzymes; extracellular stimuli; Fatty acids; Gene expression; Gene Expression Regulation; Growth factors; HEK293 Cells; Homeostasis; Hormones; Humans; Hypertrophy; Insulin; Insulin - metabolism; Intercellular Signaling Peptides and Proteins - metabolism; Investigations; Kinases; Mammalian cells; Mammals; Metabolism; Metabolites; Mutation; Neurodegeneration; Neurotransmitters; Nutrients; Oxidative Stress; Protein thiols; Proteins; Regulation; Signal Transduction; Thioesters; Thiols
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms22031131

Coenzyme A (CoA) is an essential cofactor present in all living cells. Under physiological conditions, CoA mainly functions to generate metabolically active CoA thioesters, which are indispensable for cellular metabolism, the regulation of gene expression, and the biosynthesis of neurotransmitters. When cells are exposed to oxidative or metabolic stress, CoA acts as an important cellular antioxidant that protects protein thiols from overoxidation, and this function is mediated by protein CoAlation. CoA and its derivatives are strictly maintained at levels controlled by nutrients, hormones, metabolites, and cellular stresses. Dysregulation of their biosynthesis and homeostasis has deleterious consequences and has been noted in a range of pathological conditions, including cancer, diabetes, Reye's syndrome, cardiac hypertrophy, and neurodegeneration. The biochemistry of CoA biosynthesis, which involves five enzymatic steps, has been extensively studied. However, the existence of a CoA biosynthetic complex and the mode of its regulation in mammalian cells are unknown. In this study, we report the assembly of all five enzymes that drive CoA biosynthesis, in HEK293/Pank1β and A549 cells, using the in situ proximity ligation assay. Furthermore, we show that the association of CoA biosynthetic enzymes is strongly upregulated in response to serum starvation and oxidative stress, whereas insulin and growth factor signaling downregulate their assembly.