Journal of Lipid Research (Apr 2014)

TG-interacting factor 1 acts as a transcriptional repressor of sterol O-acyltransferase 2[S]

  • Camilla Pramfalk,
  • Tiffany A. Melhuish,
  • David Wotton,
  • Zhao-Yan Jiang,
  • Mats Eriksson,
  • Paolo Parini

Journal volume & issue
Vol. 55, no. 4
pp. 709 – 717

Abstract

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Acat2 [gene name: sterol O-acyltransferase 2 (SOAT2)] esterifies cholesterol in enterocytes and hepatocytes. This study aims to identify repressor elements in the human SOAT2 promoter and evaluate their in vivo relevance. We identified TG-interacting factor 1 (Tgif1) to function as an important repressor of SOAT2. Tgif1 could also block the induction of the SOAT2 promoter activity by hepatocyte nuclear factor 1α and 4α. Women have ∼30% higher hepatic TGIF1 mRNA compared with men. Depletion of Tgif1 in mice increased the hepatic Soat2 expression and resulted in higher hepatic lipid accumulation and plasma cholesterol levels. Tgif1 is a new player in human cholesterol metabolism.

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