Abstract

C57BL/6J (B6) mice are susceptible to high-fat diet (HFD)-induced obesity and have been used in metabolism research for many decades. However, the genetic component of HFD-induced obesity has not yet been elucidated. This study reports evidence for a paternal transmission of HFD-induced obesity and a correlated expression of Igf2 and Peg3 (paternal expressed gene 3) imprinted genes. We found that PWK mice are resistant to HFD-induced obesity compared to C57BL/6J mice. Therefore, we generated and analyzed reciprocal crosses between these mice, namely; (PWK×B6) F1 progeny with B6 father and (B6×PWK) F1 progeny with PWK father. The (PWK×B6) F1 mice were more sensitive to diet-induced obesity compared to (B6×PWK) F1 mice, suggesting a paternal transmission of diet-induced obesity. Expression analysis of imprinted genes in adipocytes revealed that HFD influences the expression of some of the imprinted genes in adipose tissue in B6 and PWK mice. Interestingly, Igf2 and Peg3, which are paternally expressed imprinted genes involved in the regulation of body fat accumulation, were down-regulated in B6 and (PWK×B6) F1 mice, which are susceptible to HFD-induced obesity, but not in PWK and (B6×PWK) F1 mice, which are resistant. Furthermore, in vitro analysis showed that Igf2, but not Peg3, had an anti-inflammatory effect on TNF-α induced MCP-1 expression in adipocytes. Taken together, our findings suggest that the down-regulation of Igf2 and Peg3 imprinted genes in adipocytes may be involved in the paternal transmission of HFD-induced obesity.

Highlights

  • In mammals, the maternal and paternal genomes are not functionally equivalent

  • We report evidence for paternal transmission of high-fat diet (HFD)-induced obesity, which correlated with the expression of Peg3 and Igf2 imprinted genes

  • We found that PWK mice are resistant to HFD-induced obesity compared to C57BL/6J (B6) mice

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Summary

Introduction

The maternal and paternal genomes are not functionally equivalent This is due to a small number of genes called imprinted genes, which exhibit the parental allele-specific expression. Genetic disorders affecting imprinted genes lead to obesity. Prader-Willi syndrome (PWS) is a genetic disorder resulting from the loss of expression of a cluster of paternally expressed genes on chromosome 15q11-q13 [1], which leads to obesity. Peg1/Mest is a paternally-expressed gene1/ mesoderm-specific transcript, which promotes adipogenesis and obesity when overexpressed [2,3]. Peg knockout mice are characterized by increased body fat [7]. Other imprinted genes, such as Igf, Igf2r, and p57Kip, may be involved in the regulation of adipocyte growth [8]

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