Figure 3
Figure 3. CYTIP is degraded via the proteasome, and vhs and ICP0 do not contribute to its degradation. Western blot analyses were performed with an antibody specific for CYTIP. Infection with either a vhs deletion mutant virus (A) or an ICP0 deletion mutant (C) leads to degradation of CYTIP with kinetics similar to that of HSV-1 wild-type infection. DCs were infected at a MOI of 1 and harvested at the indicated time points after infection (pi). (B) Inhibition of the proteasome by the addition of 10 μM MG-132 beginning 1 hour after infection completely blocks the loss of CYTIP. Notably, an additional band with higher molecular weight accumulates in MG-132-treated samples. The enrichment of this band in HSV-1–infected DCs indicates a modification that is marked for degradation. Experiments were performed at least 3 times independently, and 1 representative experiment is shown.

CYTIP is degraded via the proteasome, and vhs and ICP0 do not contribute to its degradation. Western blot analyses were performed with an antibody specific for CYTIP. Infection with either a vhs deletion mutant virus (A) or an ICP0 deletion mutant (C) leads to degradation of CYTIP with kinetics similar to that of HSV-1 wild-type infection. DCs were infected at a MOI of 1 and harvested at the indicated time points after infection (pi). (B) Inhibition of the proteasome by the addition of 10 μM MG-132 beginning 1 hour after infection completely blocks the loss of CYTIP. Notably, an additional band with higher molecular weight accumulates in MG-132-treated samples. The enrichment of this band in HSV-1–infected DCs indicates a modification that is marked for degradation. Experiments were performed at least 3 times independently, and 1 representative experiment is shown.

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