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A yeast mutant defective at an early stage in import of secretory protein precursors into the endoplasmic reticulum

We have devised a genetic selection for mutant yeast cells that fail to translocate secretory protein precursors into the lumen of the endoplasmic reticulum (ER). Mutant cells are selected by a procedure that requires a signal peptide-containing cytoplasmic enzyme chimera to remain in contact with t...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1987
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2114772/
https://www.ncbi.nlm.nih.gov/pubmed/3305520
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collection PubMed
description We have devised a genetic selection for mutant yeast cells that fail to translocate secretory protein precursors into the lumen of the endoplasmic reticulum (ER). Mutant cells are selected by a procedure that requires a signal peptide-containing cytoplasmic enzyme chimera to remain in contact with the cytosol. This approach has uncovered a new secretory mutant, sec61, that is thermosensitive for growth and that accumulates multiple secretory and vacuolar precursor proteins that have not acquired any detectable posttranslational modifications associated with translocation into the ER. Preproteins that accumulate at the sec61 block sediment with the particulate fraction, but are exposed to the cytosol as judged by sensitivity to proteinase K. Thus, the sec61 mutation defines a gene that is required for an early cytoplasmic or ER membrane-associated step in protein translocation.
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spelling pubmed-21147722008-05-01 A yeast mutant defective at an early stage in import of secretory protein precursors into the endoplasmic reticulum J Cell Biol Articles We have devised a genetic selection for mutant yeast cells that fail to translocate secretory protein precursors into the lumen of the endoplasmic reticulum (ER). Mutant cells are selected by a procedure that requires a signal peptide-containing cytoplasmic enzyme chimera to remain in contact with the cytosol. This approach has uncovered a new secretory mutant, sec61, that is thermosensitive for growth and that accumulates multiple secretory and vacuolar precursor proteins that have not acquired any detectable posttranslational modifications associated with translocation into the ER. Preproteins that accumulate at the sec61 block sediment with the particulate fraction, but are exposed to the cytosol as judged by sensitivity to proteinase K. Thus, the sec61 mutation defines a gene that is required for an early cytoplasmic or ER membrane-associated step in protein translocation. The Rockefeller University Press 1987-08-01 /pmc/articles/PMC2114772/ /pubmed/3305520 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
A yeast mutant defective at an early stage in import of secretory protein precursors into the endoplasmic reticulum
title A yeast mutant defective at an early stage in import of secretory protein precursors into the endoplasmic reticulum
title_full A yeast mutant defective at an early stage in import of secretory protein precursors into the endoplasmic reticulum
title_fullStr A yeast mutant defective at an early stage in import of secretory protein precursors into the endoplasmic reticulum
title_full_unstemmed A yeast mutant defective at an early stage in import of secretory protein precursors into the endoplasmic reticulum
title_short A yeast mutant defective at an early stage in import of secretory protein precursors into the endoplasmic reticulum
title_sort yeast mutant defective at an early stage in import of secretory protein precursors into the endoplasmic reticulum
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2114772/
https://www.ncbi.nlm.nih.gov/pubmed/3305520