1998
DOI: 10.1093/emboj/17.10.2759
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Degradation signals for ubiquitin system proteolysis in Saccharomyces cerevisiae

Abstract: Combinations of different ubiquitin-conjugating (Ubc) enzymes and other factors constitute subsidiary pathways of the ubiquitin system, each of which ubiquitinates a specific subset of proteins. There is evidence that certain sequence elements or structural motifs of target proteins are degradation signals which mark them for ubiquitination by a particular branch of the ubiquitin system and for subsequent degradation. Our aim was to devise a way of searching systematically for degradation signals and to determ… Show more

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Cited by 210 publications
(217 citation statements)
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“…We developed an assay for testing the effect of compounds on mutant Htt-induced proteasome dysfunction and tested the effects of compounds B1-B5 in this assay. A CHO-K1 cell line was generated that stably expresses both a reporter of proteasome function (EGFP fused to the degradation signal peptide CL1) (15) and the first exon of Htt (with mutant 97Q) fused to monomeric red fluorescent protein (mRFP) ( Fig. 2A).…”
Section: Resultsmentioning
confidence: 99%
“…We developed an assay for testing the effect of compounds on mutant Htt-induced proteasome dysfunction and tested the effects of compounds B1-B5 in this assay. A CHO-K1 cell line was generated that stably expresses both a reporter of proteasome function (EGFP fused to the degradation signal peptide CL1) (15) and the first exon of Htt (with mutant 97Q) fused to monomeric red fluorescent protein (mRFP) ( Fig. 2A).…”
Section: Resultsmentioning
confidence: 99%
“…By appending a short degron sequence, CL1 12 to the C terminus of GFP, the protein is constitutively degraded by the proteasome; this fusion protein is referred to as GFP u . 13 Rat 6 fibroblasts (5 Â 10 6 ) were mixed gently with 3 mg of GFP u DNA, 13 electroporated with a Nucleofector Kit Number V for cell lines according to the manual (Amaxa; Köln; Germany).…”
Section: Methodsmentioning
confidence: 99%
“…This is the same E2 enzyme that we show below to mediate degradation of Hac1p. Because other degradation signals target a similar Ura3/HA fusion protein to different E2 enzymes such as Ubc6p and/or Ubc7p (Gilon et al, 1998), our data suggest that residues 122-158 of Hac1p contain a specific recognition signal for Ubc3p/Cdc34p. …”
mentioning
confidence: 86%