The proteasome is a multisubunit proteolytic enzyme comprising activator complexes bound to the 20 S catalytic core. The functions of the proteasomal activator (PA) 700 in ubiquitin/ATP-dependent protein degradation and of the PA28α/β activators in antigen presentation are well defined. However, the function of a third PA, PA28γ, remains elusive. We now show that mitogen-activated protein kinase (MAPK)/extracellular-signal-regulated kinase (ERK) kinase kinase 3 (MEKK3), a MAPK kinase kinase (MAPKKK) involved in MAPK kinase 7 (MKK7)–c-Jun N-terminal kinase (‘JNK’) and MKK6–p38 signalling, can bind PA28γ but not PA28α. In contrast, B-Raf, a MAPKKK specific for the MAPK/ERK kinase (‘MEK’)–ERK module, binds PA28γ and α. The PA28γ-binding domain of MEKK3 is located within its N-terminal regulatory domain (amino acids 1–178). Expression of MEKK3 in Cos-7 cells led to an increase in endogenous and co-expressed PA28γ protein levels, whereas kinase-deficient MEKK3 had no effect on PA28γ expression. Furthermore, in vitro assays indicated that PA28γ was a MEKK3 substrate. MEKK3 represents the first protein kinase capable of binding and phosphorylating a PA, and provides a potential mechanism to link stress-activated protein kinase signalling with the PA28γ-dependent proteasome.

HAGEMANN, C., PATEL, R., & BLANK, J. L. (2003). MEKK3 interacts with the PA28gamma regulatory subunit of the proteasome. Biochemical Journal, 373(1), 71–79.