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A fast and efficient translational control system for conditional expression of yeast genes

  • A new artificial regulatory system for essential genes in yeast is described. It prevents translation of target mRNAs upon tetracycline (tc) binding to aptamers introduced into their 5'UTRs. Exploiting direct RNA–ligand interaction renders auxiliary protein factors unnecessary. Therefore, our approach is strain independent and not susceptible to interferences by heterologous expressed regulatory proteins. We use a simple PCR-based strategy, which allows easy tagging of any target gene and the level of gene expression can be adjusted due to various tc aptamer-regulated promoters. As proof of concept, five differently expressed genes were targeted, two of which could not be regulated previously. In all cases, adding tc completely prevented growth and, as shown for Nop14p, rapidly abolished de novo protein synthesis providing a powerful tool for conditional regulation of yeast gene expression.

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Verfasserangaben:Peter KötterORCiD, Julia E. WeigandORCiDGND, Britta Meyer, Karl-Dieter Entian, Beatrix SüßGND
URN:urn:nbn:de:hebis:30-80630
DOI:https://doi.org/10.1093/nar/gkp578
ISSN:0301-5610
ISSN:0305-1048
Pubmed-Id:https://pubmed.ncbi.nlm.nih.gov/19592423
Titel des übergeordneten Werkes (Englisch):Nucleic acids research
Verlag:Oxford Univ. Press
Verlagsort:Oxford
Dokumentart:Wissenschaftlicher Artikel
Sprache:Englisch
Datum der Veröffentlichung (online):10.07.2009
Datum der Erstveröffentlichung:10.07.2009
Veröffentlichende Institution:Universitätsbibliothek Johann Christian Senckenberg
Datum der Freischaltung:24.09.2010
Jahrgang:37
Ausgabe / Heft:(18): e120
Seitenzahl:7
Erste Seite:1
Letzte Seite:7
Bemerkung:
©  2009 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Quelle:Nucleic acids research, Vol. 37, No. 18 e120 ; doi:10.1093/nar/gkp578 ; http://nar.oxfordjournals.org/content/37/18/e120.abstract
HeBIS-PPN:228850614
Institute:Biowissenschaften / Biowissenschaften
DDC-Klassifikation:5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Sammlungen:Universitätspublikationen
Sammlung Biologie / Sondersammelgebiets-Volltexte
Lizenz (Deutsch):License LogoCreative Commons - Namensnennung-Nicht kommerziell 2.0