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A genome-scale CRISPR interference guide library enables comprehensive phenotypic profiling in yeast

BACKGROUND: CRISPR/Cas9-mediated transcriptional interference (CRISPRi) enables programmable gene knock-down, yielding loss-of-function phenotypes for nearly any gene. Effective, inducible CRISPRi has been demonstrated in budding yeast, and genome-scale guide libraries enable systematic, genome-wide...

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Autores principales: McGlincy, Nicholas J., Meacham, Zuriah A., Reynaud, Kendra K., Muller, Ryan, Baum, Rachel, Ingolia, Nicholas T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986282/
https://www.ncbi.nlm.nih.gov/pubmed/33757429
http://dx.doi.org/10.1186/s12864-021-07518-0
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author McGlincy, Nicholas J.
Meacham, Zuriah A.
Reynaud, Kendra K.
Muller, Ryan
Baum, Rachel
Ingolia, Nicholas T.
author_facet McGlincy, Nicholas J.
Meacham, Zuriah A.
Reynaud, Kendra K.
Muller, Ryan
Baum, Rachel
Ingolia, Nicholas T.
author_sort McGlincy, Nicholas J.
collection PubMed
description BACKGROUND: CRISPR/Cas9-mediated transcriptional interference (CRISPRi) enables programmable gene knock-down, yielding loss-of-function phenotypes for nearly any gene. Effective, inducible CRISPRi has been demonstrated in budding yeast, and genome-scale guide libraries enable systematic, genome-wide genetic analysis. RESULTS: We present a comprehensive yeast CRISPRi library, based on empirical design rules, containing 10 distinct guides for most genes. Competitive growth after pooled transformation revealed strong fitness defects for most essential genes, verifying that the library provides comprehensive genome coverage. We used the relative growth defects caused by different guides targeting essential genes to further refine yeast CRISPRi design rules. In order to obtain more accurate and robust guide abundance measurements in pooled screens, we link guides with random nucleotide barcodes and carry out linear amplification by in vitro transcription. CONCLUSIONS: Taken together, we demonstrate a broadly useful platform for comprehensive, high-precision CRISPRi screening in yeast. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07518-0.
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spelling pubmed-79862822021-03-24 A genome-scale CRISPR interference guide library enables comprehensive phenotypic profiling in yeast McGlincy, Nicholas J. Meacham, Zuriah A. Reynaud, Kendra K. Muller, Ryan Baum, Rachel Ingolia, Nicholas T. BMC Genomics Methodology Article BACKGROUND: CRISPR/Cas9-mediated transcriptional interference (CRISPRi) enables programmable gene knock-down, yielding loss-of-function phenotypes for nearly any gene. Effective, inducible CRISPRi has been demonstrated in budding yeast, and genome-scale guide libraries enable systematic, genome-wide genetic analysis. RESULTS: We present a comprehensive yeast CRISPRi library, based on empirical design rules, containing 10 distinct guides for most genes. Competitive growth after pooled transformation revealed strong fitness defects for most essential genes, verifying that the library provides comprehensive genome coverage. We used the relative growth defects caused by different guides targeting essential genes to further refine yeast CRISPRi design rules. In order to obtain more accurate and robust guide abundance measurements in pooled screens, we link guides with random nucleotide barcodes and carry out linear amplification by in vitro transcription. CONCLUSIONS: Taken together, we demonstrate a broadly useful platform for comprehensive, high-precision CRISPRi screening in yeast. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07518-0. BioMed Central 2021-03-23 /pmc/articles/PMC7986282/ /pubmed/33757429 http://dx.doi.org/10.1186/s12864-021-07518-0 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology Article
McGlincy, Nicholas J.
Meacham, Zuriah A.
Reynaud, Kendra K.
Muller, Ryan
Baum, Rachel
Ingolia, Nicholas T.
A genome-scale CRISPR interference guide library enables comprehensive phenotypic profiling in yeast
title A genome-scale CRISPR interference guide library enables comprehensive phenotypic profiling in yeast
title_full A genome-scale CRISPR interference guide library enables comprehensive phenotypic profiling in yeast
title_fullStr A genome-scale CRISPR interference guide library enables comprehensive phenotypic profiling in yeast
title_full_unstemmed A genome-scale CRISPR interference guide library enables comprehensive phenotypic profiling in yeast
title_short A genome-scale CRISPR interference guide library enables comprehensive phenotypic profiling in yeast
title_sort genome-scale crispr interference guide library enables comprehensive phenotypic profiling in yeast
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986282/
https://www.ncbi.nlm.nih.gov/pubmed/33757429
http://dx.doi.org/10.1186/s12864-021-07518-0
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