Abstract
PDI1 is the essential gene encoding protein disulfide isomerase in yeast. The Saccharomyces cerevisiae genome, however, contains four other nonessential genes with homology to PDI1: MPD1, MPD2, EUG1, and EPS1. We have investigated the effects of simultaneous deletions of these genes. In several cases, we found that the ability of the PDI1 homologues to restore viability to a pdi1-deleted strain when overexpressed was dependent on the presence of low endogenous levels of one or more of the other homologues. This shows that the homologues are not functionally interchangeable. In fact, Mpd1p was the only homologue capable of carrying out all the essential functions of Pdi1p. Furthermore, the presence of endogenous homologues with a CXXC motif in the thioredoxin-like domain is required for suppression of a pdi1 deletion by EUG1 (which contains two CXXS active site motifs). This underlines the essentiality of protein disulfide isomerase-catalyzed oxidation. Most mutant combinations show defects in carboxypeptidase Y folding as well as in glycan modification. There are, however, no significant effects on ER-associated protein degradation in the various protein disulfide isomerase-deleted strains.
| Original language | English |
|---|---|
| Journal | Journal of Cell Biology |
| Volume | 152 |
| Issue number | 3 |
| Pages (from-to) | 553-62 |
| Number of pages | 10 |
| ISSN | 0021-9525 |
| Publication status | Published - 2001 |
Keywords
- Blotting, Western
- Dithiothreitol
- Endoplasmic Reticulum
- Escherichia coli
- Gene Deletion
- Genes, Essential
- Genes, Fungal
- Glycosylation
- Mutation
- Plasmids
- Precipitin Tests
- Protein Disulfide-Isomerases
- Protein Folding
- Saccharomyces cerevisiae