CFTR degradation in yeast is compromised in
strains defective for proteasome function and ubiquitin conjugation.
CFTR-expressing cells grown at 26°C and then incubated for 1 h
at 40°C were harvested at the indicated time points after the
addition of cycloheximide, and cell extracts were prepared and
subjected to SDS-PAGE and immunoblot analysis as described
in MATERIALS AND METHODS. Results from a quantitative
immunoblot analysis are shown. The amount of CFTR at time
zero was set to 1. ●, PRE1PRE2; ○,
pre1-1pre2-2; ▪, UBC6UBC7; □,
ubc6ubc7.