Control of iron homeostasis by an iron-regulated ubiquitin ligase.

نویسندگان

  • Ajay A Vashisht
  • Kimberly B Zumbrennen
  • Xinhua Huang
  • David N Powers
  • Armando Durazo
  • Dahui Sun
  • Nimesh Bhaskaran
  • Anja Persson
  • Mathias Uhlen
  • Olle Sangfelt
  • Charles Spruck
  • Elizabeth A Leibold
  • James A Wohlschlegel
چکیده

Eukaryotic cells require iron for survival and have developed regulatory mechanisms for maintaining appropriate intracellular iron concentrations. The degradation of iron regulatory protein 2 (IRP2) in iron-replete cells is a key event in this pathway, but the E3 ubiquitin ligase responsible for its proteolysis has remained elusive. We found that a SKP1-CUL1-FBXL5 ubiquitin ligase protein complex associates with and promotes the iron-dependent ubiquitination and degradation of IRP2. The F-box substrate adaptor protein FBXL5 was degraded upon iron and oxygen depletion in a process that required an iron-binding hemerythrin-like domain in its N terminus. Thus, iron homeostasis is regulated by a proteolytic pathway that couples IRP2 degradation to intracellular iron levels through the stability and activity of FBXL5.

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An E3 ligase possessing an iron-responsive hemerythrin domain is a regulator of iron homeostasis.

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عنوان ژورنال:
  • Science

دوره 326 5953  شماره 

صفحات  -

تاریخ انتشار 2009