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Resolution: standard / high Figure 5.
UBXN7 over-expression causes HIF1α accumulation in a UIM-dependent manner. (A) Non-ubiquitylated HIF1α accumulates in cells over-expressing wild-type Flag-UBXN7,
but not in cells expressing a UIM-deleted version. 10 μM MG132 was added two hours
prior to cell lysis to facilitate HIF1α detection. UBXN7 over-expression had no effect
on CRL2 subunit levels. (B) Over-expression of another UIM-containing protein, PSMD4, does not alter HIF1α levels.
(C, D) UIM-dependent accumulation of non-ubiquitylated HIF1α upon UBXN7 over-expression
is also observed in the absence of proteasome inhibition (right panels). Wild-type
UBXN7 interacted with HIF1α at various degrees of ubiquitylation, while UIM-defective
UBXN7 (upon UIM deletion or point mutation at Ser297) only interacted with slow-migrating,
poly-ubiquitylated HIF1α (left panels). The corresponding Flag, CUL2 and p97 western
blots for the experiment in (C) are shown in figure 3D. (D) UBXN7 mutated at Ser288 within the UIM motif binds CUL2 (left panel) and causes
HIF1α accumulation (right panel), similar to the wild-type protein. The indicated
proteins were detected using specific antibodies.
Bandau et al. BMC Biology 2012 10:36 doi:10.1186/1741-7007-10-36 |