Abstract

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.

Highlights

  • Genome-wide association studies in the FTO gene have identified single nucleotide polymorphisms (SNPs) correlating with obesity and type 2 diabetes

  • The highest Fto mRNA levels were observed in the hypothalamus, but we found that in our pigs the cerebellum was the richest source of FTO protein

  • The role of the FTO protein was practically unknown, even though FTO SNPs have been described as strong genetic factors linked to predisposition to obesity and the development of Type 2 diabetes (T2D)

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Summary

Introduction

Genome-wide association studies in the FTO gene have identified SNPs correlating with obesity and type 2 diabetes. Our data suggest that FTO protein may play a number of distinct, yet unknown intracellular functions due to its localization It may play a role in animal growth/development and metabolic state, additional studies are necessary to clarify the detailed mechanism(s) of action. Evidence from genetic epidemiology studies, life-course modeling, and diet-induced fetal programming data suggests that the FTO gene plays an important role in these complex biological interactions. It may provide the missing link in the developmental regulation of energy metabolism. Far researchers have measured the level of FTO mRNA, rather than the level of the protein, and the experiments have been performed primarily in rodents and not species with metabolisms more similar to h­ umans[40] (Supplementary Figure S1)

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