1. Academic Validation
  2. A novel mammalian endoplasmic reticulum ubiquitin ligase homologous to the yeast Hrd1

A novel mammalian endoplasmic reticulum ubiquitin ligase homologous to the yeast Hrd1

  • Biochem Biophys Res Commun. 2003 Mar 28;303(1):91-7. doi: 10.1016/s0006-291x(03)00279-1.
Eran Nadav 1 Ayelet Shmueli Haim Barr Hedva Gonen Aaron Ciechanover Yuval Reiss
Affiliations

Affiliation

  • 1 Department of Biochemistry, George S. Wise Faculty of Life sciences, Tel Aviv University, Tel Aviv 69978, Israel. [email protected]
Abstract

The yeast hHrd1 is a ubiquitin-protein ligase (E3) involved in ER-associated degradation. It was originally identified by genetic methods as an E3 of the yeast Cholesterol biosynthetic Enzyme HMG-CoA reductase (HMGR). We report the identification and cloning of a human homologue of Hrd1 (hHrd1). Immunofluorescence imaging confirms that the endogenous hHrd1 resides in the ER and in vitro assay demonstrates that it has a ubiquitin-ligase activity. However, the homology between the human and yeast Hrd1 is limited to the N-terminal domain of the proteins, and hHrd1 does not appear to be involved in the degradation of mammalian HMGR.

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