Evaluation of RNAi and CRISPR technologies by large-scale gene expression profiling in the Connectivity Map
Author(s) -
Ian C. P. Smith,
Peyton Greenside,
Ted Natoli,
David L. Lahr,
David Wadden,
Itay Tirosh,
Rajiv Narayan,
David E. Root,
Todd R. Golub,
Aravind Subramanian,
John G. Doench
Publication year - 2017
Publication title -
plos biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.127
H-Index - 271
eISSN - 1545-7885
pISSN - 1544-9173
DOI - 10.1371/journal.pbio.2003213
Subject(s) - rna interference , crispr , biology , computational biology , microrna , genetics , gene , small hairpin rna , loss function , gene expression profiling , gene expression , crispr interference , functional genomics , function (biology) , phenotype , gene knockdown , cas9 , genomics , rna , genome
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.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom