“…As in the absence of Ubc13/CHIP, where GHR is ubiquitinated to the same extent as in clathrin-depleted cells, it might indicate that Ubc13/CHIP might edit pre-existing, TrCP-derived, ubiquitin chains on GHR. The opposite could be envisioned if we consider that the WD40 propeller domain of TrCP was identified as a ubiquitin-binding domain, indicating that TrCP might also recognize a ubiquitin moiety as its substrate (57). However, if we deplete CHIP, GHR is still ubiquitinated, presumably by TrCP.…”