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© The Rockefeller University Press, 0021-9525/2002/7/91 $5.00
The Journal of Cell Biology, Volume 158, Number 1, July 8, 2002 91-102

An HRD/DER-independent ER quality control mechanism involves Rsp5p-dependent ubiquitination and ER-Golgi transport

University of Missouri-Kansas City, Division of Cell Biology and Biophysics, School of Biological Sciences, Kansas City, MO 64110

Address correspondence to Antony A. Cooper, University of Missouri-Kansas City, Division of Cell Biology and Biophysics, School of Biological Sciences, 5100 Rockhill Rd., Kansas City, MO 64110. Tel.: (816) 235-2265. Fax: (816) 235-1503. E-mail: coopera{at}umkc.edu

We have identified a new pathway of ER-associated degradation in Saccharomyces cerevisiae that functions separately from the HRD/DER pathway comprised of Hrd1p, Hrd3p, Der1p, and Ubc7p. This pathway, termed Hrd1p independent-proteolysis (HIP), is capable of recognizing and degrading both lumenal (CPY* and PrA*), and integral membrane proteins (Sec61–2p) that misfold in the ER. CPY* overexpression likely saturates the HRD/DER pathway and activates the HIP pathway, so the slowed degradation kinetics of CPY* in a hrd1 strain is restored to a wild-type rate when CPY* is overexpressed. Substrates of HIP require vesicular trafficking between the ER and Golgi apparatus before degradation by the ubiquitin-proteasome system. Ubiquitination of HIP substrates does not involve the HRD/DER pathway ubiquitin ligase Hrd1p, but instead uses another ubiquitin ligase, Rsp5p. HIP is regulated by the unfolded protein response as Ire1p is necessary for the degradation of CPY* when overexpressed, but not when CPY* is expressed at normal levels. Both the HIP and HRD/DER pathways contribute to the degradation of CPY*, and only by eliminating both is CPY* degradation completely blocked.

Key Words: endoplasmic reticulum; ER-associated degradation; degradation; ubiquitin ligase; secretory pathway

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