摘要
Proteasome-mediated degradation and autophagy are the two major pathways mediating the turnover of cellularproteins.The proteasomal pathway is known to be a highly specific and regulated process mediating the degradationof short-lived proteins such as many important factors involved in cellular signaling.In contrast,it is generally thoughtthat autophagy is rather nonselective as it is responsible for the bulk degradation of long-lived proteins and organelles.Challenging this general view,in this issue of Cell Research,Qing et al.report that selective degradation of the IκBkinase(IKK)triggered by the loss of Hsp90 function is mediated by autophagy[1].
Proteasome-mediated degradation and autophagy are the two major pathways mediating the turnover of cellular proteins. The proteasomal pathway is known to be a highly specific and regulated process mediating the degradation of short-lived proteins such as many important factors involved in cellular signaling. In contrast, it is generally thought that autophagy is rather nonselective as it is responsible for the bulk degradation of long-lived proteins and organelles. Challenging this general view, in this issue of Cell Research, Qing et al. report that selective degradation of the IκB kinase （IKK） triggered by the loss of Hsp90 function is mediated by autophagy [1].
