Identification of IRS-1 Ser-1101 as a target of S6K1 in nutrient- and obesity-induced insulin resistance

Frédéric Tremblay(Université Laval), Sophie Brûlé(Université Laval), Sung Hee Um(University of Cincinnati), Yu Li(Cell Signaling Technology (United States)), Kohei Masuda(University of Cincinnati), Michael Roden(Hanusch Hospital), Xiao‐Jian Sun(University of Chicago), Michael Krebs(Medical University of Vienna), Roberto D. Polakiewicz(Cell Signaling Technology (United States)), George Thomas(University of Cincinnati), André Marette(Université Laval)
Proceedings of the National Academy of Sciences
August 21, 2007
Cited by 463Open Access
Full Text

Abstract

S6K1 has emerged as a critical signaling component in the development of insulin resistance through phosphorylation and inhibition of IRS-1 function. This effect can be triggered directly by nutrients such as amino acids or by insulin through a homeostatic negative-feedback loop. However, the role of S6K1 in mediating IRS-1 phosphorylation in a physiological setting of nutrient overload is unresolved. Here we show that S6K1 directly phosphorylates IRS-1 Ser-1101 in vitro in the C-terminal domain of the protein and that mutation of this site largely blocks the ability of amino acids to suppress IRS-1 tyrosine and Akt phosphorylation. Consistent with this finding, phosphorylation of IRS-1 Ser-1101 is increased in the liver of obese db/db and wild-type, but not S6K1(-/-), mice maintained on a high-fat diet and is blocked by siRNA knockdown of S6K1 protein. Finally, infusion of amino acids in humans leads to the concomitant activation of S6K1, phosphorylation of IRS-1 Ser-1101, a reduction in IRS-1 function, and insulin resistance in skeletal muscle. These findings indicate that nutrient- and hormonal-dependent activation of S6K1 causes insulin resistance in mice and humans, in part, by mediating IRS-1 Ser-1101 phosphorylation.


Related Papers