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Setting of graded levels of a protein in yeast by a t-degron technique as applied to phosphoglycerate mutase

BACKGROUND: Setting of graded levels of a protein for in vivo studies by controlled gene expression has inconveniences, and we here explore the use of the t-degron technique instead. RESULTS: In a yeast t-degron (ubiquitin-argDHFR(ts))- phosphoglycerate mutase (GPM1) fusion strain, increasing period...

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Autores principales: Heidrich, Katja, Fraenkel, Dan G
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC117797/
https://www.ncbi.nlm.nih.gov/pubmed/12149134
http://dx.doi.org/10.1186/1471-2156-3-13
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author Heidrich, Katja
Fraenkel, Dan G
author_facet Heidrich, Katja
Fraenkel, Dan G
author_sort Heidrich, Katja
collection PubMed
description BACKGROUND: Setting of graded levels of a protein for in vivo studies by controlled gene expression has inconveniences, and we here explore the use of the t-degron technique instead. RESULTS: In a yeast t-degron (ubiquitin-argDHFR(ts))- phosphoglycerate mutase (GPM1) fusion strain, increasing periods of exposure to the non-permissive temperature 37°C, even in the presence of cycloheximide, gave decreasing function, as assessed at 23°C in vivo by glucose metabolism and confirmed by immunoblot. CONCLUSION: An ideal system would set a range of lower levels of a protein, do so without compensating protein synthesis, and give stable activity for in vitro comparisons. Although the first two aims appear obtainable, the third was not in this example of the application, limiting its uses for some but not all purposes.
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spelling pubmed-1177972002-08-14 Setting of graded levels of a protein in yeast by a t-degron technique as applied to phosphoglycerate mutase Heidrich, Katja Fraenkel, Dan G BMC Genet Methodology Article BACKGROUND: Setting of graded levels of a protein for in vivo studies by controlled gene expression has inconveniences, and we here explore the use of the t-degron technique instead. RESULTS: In a yeast t-degron (ubiquitin-argDHFR(ts))- phosphoglycerate mutase (GPM1) fusion strain, increasing periods of exposure to the non-permissive temperature 37°C, even in the presence of cycloheximide, gave decreasing function, as assessed at 23°C in vivo by glucose metabolism and confirmed by immunoblot. CONCLUSION: An ideal system would set a range of lower levels of a protein, do so without compensating protein synthesis, and give stable activity for in vitro comparisons. Although the first two aims appear obtainable, the third was not in this example of the application, limiting its uses for some but not all purposes. BioMed Central 2002-07-30 /pmc/articles/PMC117797/ /pubmed/12149134 http://dx.doi.org/10.1186/1471-2156-3-13 Text en Copyright © 2002 Heidrich and Fraenkel; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Methodology Article
Heidrich, Katja
Fraenkel, Dan G
Setting of graded levels of a protein in yeast by a t-degron technique as applied to phosphoglycerate mutase
title Setting of graded levels of a protein in yeast by a t-degron technique as applied to phosphoglycerate mutase
title_full Setting of graded levels of a protein in yeast by a t-degron technique as applied to phosphoglycerate mutase
title_fullStr Setting of graded levels of a protein in yeast by a t-degron technique as applied to phosphoglycerate mutase
title_full_unstemmed Setting of graded levels of a protein in yeast by a t-degron technique as applied to phosphoglycerate mutase
title_short Setting of graded levels of a protein in yeast by a t-degron technique as applied to phosphoglycerate mutase
title_sort setting of graded levels of a protein in yeast by a t-degron technique as applied to phosphoglycerate mutase
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC117797/
https://www.ncbi.nlm.nih.gov/pubmed/12149134
http://dx.doi.org/10.1186/1471-2156-3-13
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