Removal of damaged proteins during ES cell fate specification requires the proteasome activator PA28.

Malin Hernebring, Åsa Fredriksson, Maria Liljevald, Marija Cvijovic, Karin Norrman, John Wiseman, Henrik Semb, Thomas Nyström

Scientific reports 2013

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In embryonic stem cells, removal of oxidatively damaged proteins is triggered upon the first signs of cell fate specification but the underlying mechanism is not known. Here, we report that this phase of differentiation encompasses an unexpected induction of genes encoding the proteasome activator PA28αβ (11S), subunits of the immunoproteasome (20Si), and the 20Si regulator TNFα. This induction is accompanied by assembly of mature PA28-20S(i) proteasomes and elevated proteasome activity. Inhibiting accumulation of PA28α using miRNA counteracted the removal of damaged proteins demonstrating that PA28αβ has a hitherto unidentified role required for resetting the levels of protein damage at the transition from self-renewal to cell differentiation.

Citation

Malin Hernebring, Åsa Fredriksson, Maria Liljevald, Marija Cvijovic, Karin Norrman, John Wiseman, Henrik Semb, Thomas Nyström. Removal of damaged proteins during ES cell fate specification requires the proteasome activator PA28. Scientific reports. 2013;3:1381