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Global mapping of translation initiation sites by TIS profiling in budding yeast

Translation initiation site (TIS) profiling allows for the genome-wide identification of TISs in vivo by exclusively capturing mRNA fragments within ribosomes that have just completed translation initiation. It leverages translation inhibitors, such as harringtonine and lactimidomycin (LTM), that pr...

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Autores principales: Hollerer, Ina, Powers, Emily N., Brar, Gloria A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7797918/
https://www.ncbi.nlm.nih.gov/pubmed/33458709
http://dx.doi.org/10.1016/j.xpro.2020.100250
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author Hollerer, Ina
Powers, Emily N.
Brar, Gloria A.
author_facet Hollerer, Ina
Powers, Emily N.
Brar, Gloria A.
author_sort Hollerer, Ina
collection PubMed
description Translation initiation site (TIS) profiling allows for the genome-wide identification of TISs in vivo by exclusively capturing mRNA fragments within ribosomes that have just completed translation initiation. It leverages translation inhibitors, such as harringtonine and lactimidomycin (LTM), that preferentially capture ribosomes at start codon positions, protecting TIS-derived mRNA fragments from nuclease digestion. Here, we describe a step-by-step protocol for TIS profiling in LTM-treated budding yeast that we developed to identify TISs and open reading frames in vegetative and meiotic cells. For complete details on the use and execution of this protocol, please refer to Eisenberg et al. (2020).
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spelling pubmed-77979182021-01-15 Global mapping of translation initiation sites by TIS profiling in budding yeast Hollerer, Ina Powers, Emily N. Brar, Gloria A. STAR Protoc Protocol Translation initiation site (TIS) profiling allows for the genome-wide identification of TISs in vivo by exclusively capturing mRNA fragments within ribosomes that have just completed translation initiation. It leverages translation inhibitors, such as harringtonine and lactimidomycin (LTM), that preferentially capture ribosomes at start codon positions, protecting TIS-derived mRNA fragments from nuclease digestion. Here, we describe a step-by-step protocol for TIS profiling in LTM-treated budding yeast that we developed to identify TISs and open reading frames in vegetative and meiotic cells. For complete details on the use and execution of this protocol, please refer to Eisenberg et al. (2020). Elsevier 2020-12-30 /pmc/articles/PMC7797918/ /pubmed/33458709 http://dx.doi.org/10.1016/j.xpro.2020.100250 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Hollerer, Ina
Powers, Emily N.
Brar, Gloria A.
Global mapping of translation initiation sites by TIS profiling in budding yeast
title Global mapping of translation initiation sites by TIS profiling in budding yeast
title_full Global mapping of translation initiation sites by TIS profiling in budding yeast
title_fullStr Global mapping of translation initiation sites by TIS profiling in budding yeast
title_full_unstemmed Global mapping of translation initiation sites by TIS profiling in budding yeast
title_short Global mapping of translation initiation sites by TIS profiling in budding yeast
title_sort global mapping of translation initiation sites by tis profiling in budding yeast
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7797918/
https://www.ncbi.nlm.nih.gov/pubmed/33458709
http://dx.doi.org/10.1016/j.xpro.2020.100250
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