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The MARCHF6 E3 ubiquitin ligase acts as an NADPH sensor for the regula…

  • 첨부된 파일이 없습니다.
  • 저널명Nat Cell Biol . 2022 Aug;24(8):1239-1251
    • 담당교수Cheol-Sang Hwang, Yoontae Lee
    • 조회157
    • 작성자최고관리자
    • 2022-09-14


    ■ Abstract

    Ferroptosis is a unique form of cell death caused by excessive iron-dependent lipid peroxidation. The level of the anabolic reductant NADPH is a biomarker of ferroptosis sensitivity. However, specific regulators that detect cellular NADPH levels, thereby modulating downstream ferroptosis cascades, are largely unknown. We show here that the transmembrane endoplasmic reticulum MARCHF6 E3 ubiquitin ligase recognizes NADPH through its C-terminal regulatory region. This interaction upregulates the E3 ligase activity of MARCHF6, thus downregulating ferroptosis. We also found that MARCHF6 mediates the degradation of the key ferroptosis effectors ACSL4 and p53. Furthermore, inhibiting ferroptosis rescued the growth of MARCHF6-deficient tumours and peri-natal lethality of Marchf6-/- mice. Together, these findings identify MARCHF6 as a previously unknown NADPH sensor in the ubiquitin system and a crucial regulator of ferroptosis.