Evaluation of RNAi and CRISPR technologies by large-scale gene expression profiling in the Connectivity Map.

The application of RNA interference (RNAi) to mammalian cells has provided the means to perform phenotypic screens to determine the functions of genes. Although RNAi has revolutionized loss-of-function genetic experiments, it has been difficult to systematically assess the prevalence and consequence...

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Main Authors: Ian Smith, Peyton G Greenside, Ted Natoli, David L Lahr, David Wadden, Itay Tirosh, Rajiv Narayan, David E Root, Todd R Golub, Aravind Subramanian, John G Doench
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-11-01
Series:PLoS Biology
Online Access:http://europepmc.org/articles/PMC5726721?pdf=render
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spelling doaj-82e3a0766aa34da98e8d13fb5dd3c2322021-07-02T13:42:21ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852017-11-011511e200321310.1371/journal.pbio.2003213Evaluation of RNAi and CRISPR technologies by large-scale gene expression profiling in the Connectivity Map.Ian SmithPeyton G GreensideTed NatoliDavid L LahrDavid WaddenItay TiroshRajiv NarayanDavid E RootTodd R GolubAravind SubramanianJohn G DoenchThe application of RNA interference (RNAi) to mammalian cells has provided the means to perform phenotypic screens to determine the functions of genes. Although RNAi has revolutionized loss-of-function genetic experiments, it has been difficult to systematically assess the prevalence and consequences of off-target effects. The Connectivity Map (CMAP) represents an unprecedented resource to study the gene expression consequences of expressing short hairpin RNAs (shRNAs). Analysis of signatures for over 13,000 shRNAs applied in 9 cell lines revealed that microRNA (miRNA)-like off-target effects of RNAi are far stronger and more pervasive than generally appreciated. We show that mitigating off-target effects is feasible in these datasets via computational methodologies to produce a consensus gene signature (CGS). In addition, we compared RNAi technology to clustered regularly interspaced short palindromic repeat (CRISPR)-based knockout by analysis of 373 single guide RNAs (sgRNAs) in 6 cells lines and show that the on-target efficacies are comparable, but CRISPR technology is far less susceptible to systematic off-target effects. These results will help guide the proper use and analysis of loss-of-function reagents for the determination of gene function.http://europepmc.org/articles/PMC5726721?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ian Smith
Peyton G Greenside
Ted Natoli
David L Lahr
David Wadden
Itay Tirosh
Rajiv Narayan
David E Root
Todd R Golub
Aravind Subramanian
John G Doench
spellingShingle Ian Smith
Peyton G Greenside
Ted Natoli
David L Lahr
David Wadden
Itay Tirosh
Rajiv Narayan
David E Root
Todd R Golub
Aravind Subramanian
John G Doench
Evaluation of RNAi and CRISPR technologies by large-scale gene expression profiling in the Connectivity Map.
PLoS Biology
author_facet Ian Smith
Peyton G Greenside
Ted Natoli
David L Lahr
David Wadden
Itay Tirosh
Rajiv Narayan
David E Root
Todd R Golub
Aravind Subramanian
John G Doench
author_sort Ian Smith
title Evaluation of RNAi and CRISPR technologies by large-scale gene expression profiling in the Connectivity Map.
title_short Evaluation of RNAi and CRISPR technologies by large-scale gene expression profiling in the Connectivity Map.
title_full Evaluation of RNAi and CRISPR technologies by large-scale gene expression profiling in the Connectivity Map.
title_fullStr Evaluation of RNAi and CRISPR technologies by large-scale gene expression profiling in the Connectivity Map.
title_full_unstemmed Evaluation of RNAi and CRISPR technologies by large-scale gene expression profiling in the Connectivity Map.
title_sort evaluation of rnai and crispr technologies by large-scale gene expression profiling in the connectivity map.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2017-11-01
description The application of RNA interference (RNAi) to mammalian cells has provided the means to perform phenotypic screens to determine the functions of genes. Although RNAi has revolutionized loss-of-function genetic experiments, it has been difficult to systematically assess the prevalence and consequences of off-target effects. The Connectivity Map (CMAP) represents an unprecedented resource to study the gene expression consequences of expressing short hairpin RNAs (shRNAs). Analysis of signatures for over 13,000 shRNAs applied in 9 cell lines revealed that microRNA (miRNA)-like off-target effects of RNAi are far stronger and more pervasive than generally appreciated. We show that mitigating off-target effects is feasible in these datasets via computational methodologies to produce a consensus gene signature (CGS). In addition, we compared RNAi technology to clustered regularly interspaced short palindromic repeat (CRISPR)-based knockout by analysis of 373 single guide RNAs (sgRNAs) in 6 cells lines and show that the on-target efficacies are comparable, but CRISPR technology is far less susceptible to systematic off-target effects. These results will help guide the proper use and analysis of loss-of-function reagents for the determination of gene function.
url http://europepmc.org/articles/PMC5726721?pdf=render
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