Intracellular and tissue specific expression of FTO protein in pig: changes with age, energy intake and metabolic status

• Published in: Scientific reports 2020-08, Vol.10 (1), p.13029-13029, Article 13029
• Main Authors: Ferenc, Karolina, Pilžys, Tomaš, Garbicz, Damian, Marcinkowski, Michał, Skorobogatov, Oleksandr, Dylewska, Małgorzata, Gajewski, Zdzisław, Grzesiuk, Elżbieta, Zabielski, Romuald
• Format: Article
• Language: English
• Subjects: 631/1647; 631/1647/245; 631/1647/328; 631/1647/334; 631/45; 631/45/612; 631/601; 631/601/1737; 692/699; Age; Aging - metabolism; Alpha-Ketoglutarate-Dependent Dioxygenase FTO - genetics; Alpha-Ketoglutarate-Dependent Dioxygenase FTO - metabolism; Animal growth; Animals; Animals, Newborn; Beta cells; Bile; Body weight; Cell interactions; Cerebellum; Cytoplasm; Diabetes mellitus (non-insulin dependent); Diet; Energy Intake; Female; Fetal Growth Retardation - metabolism; Fto gene; Gene Frequency - genetics; Genome-wide association studies; Genomes; Growth rate; HeLa Cells; Hogs; Humanities and Social Sciences; Humans; Insulin - metabolism; Insulin-Secreting Cells - metabolism; Intracellular; Intracellular Space - metabolism; Kidneys; Localization; Male; Metabolism; multidisciplinary; Muscles; Organ Specificity; Pancreas; Phenotypes; Polymorphism, Single Nucleotide - genetics; Protein expression; Proteins; Saliva; Salivary gland; Science; Science (multidisciplinary); Single-nucleotide polymorphism; Swine; Swine - metabolism
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-69856-5

Genome-wide association studies in the FTO gene have identified SNPs correlating with obesity and type 2 diabetes. In mice, lack of Fto function leads to intrauterine growth retardation and lean phenotype, whereas in human it is lethal. The aim of this study in a pig model was to determine the localization of the FTO protein in different tissues and cell compartments, in order to investigate potential targets of FTO action. To better understand physiological role of FTO protein, its expression was studied in pigs of different age, metabolic status and nutrition, using both microscopic methods and Western blot analysis. For the first time, FTO protein was found in vivo in the cytoplasm, of not all, but specific tissues and cells e.g. in the pancreatic β-cells. Abundant FTO protein expression was found in the cerebellum, salivary gland and kidney of adult pigs. No FTO protein expression was detected in blood, saliva, and bile, excluding its role in cell-to-cell communication. In the pancreas, FTO protein expression was positively associated with energy intake, whereas in the muscles it was strictly age-related. In IUGR piglets, FTO protein expression was much higher in the cerebellum and kidneys, as compared to normal birth body weight littermates. In conclusion, our data suggest that FTO protein may play a number of distinct, yet unknown intracellular functions due to its localization. Moreover, it may play a role in animal growth/development and metabolic state, although additional studies are necessary to clarify the detailed mechanism(s) of action.