Maximizing CRISPRi efficacy and accessibility with dual-sgRNA libraries and optimal effectors

Bibliographic Details
Title: Maximizing CRISPRi efficacy and accessibility with dual-sgRNA libraries and optimal effectors
Authors: Joseph M Replogle, Jessica L Bonnar, Angela N Pogson, Christina R Liem, Nolan K Maier, Yufang Ding, Baylee J Russell, Xingren Wang, Kun Leng, Alina Guna, Thomas M Norman, Ryan A Pak, Daniel M Ramos, Michael E Ward, Luke A Gilbert, Martin Kampmann, Jonathan S Weissman, Marco Jost
Source: eLife, Vol 11 (2022)
Publisher Information: eLife Sciences Publications Ltd, 2022.
Publication Year: 2022
Collection: LCC:Medicine
LCC:Science
LCC:Biology (General)
Subject Terms: CRISPR, CRISPR interference, genetic screen, functional genomics, knockdown, Medicine, Science, Biology (General), QH301-705.5
More Details: CRISPR interference (CRISPRi) enables programmable, reversible, and titratable repression of gene expression (knockdown) in mammalian cells. Initial CRISPRi-mediated genetic screens have showcased the potential to address basic questions in cell biology, genetics, and biotechnology, but wider deployment of CRISPRi screening has been constrained by the large size of single guide RNA (sgRNA) libraries and challenges in generating cell models with consistent CRISPRi-mediated knockdown. Here, we present next-generation CRISPRi sgRNA libraries and effector expression constructs that enable strong and consistent knockdown across mammalian cell models. First, we combine empirical sgRNA selection with a dual-sgRNA library design to generate an ultra-compact (1–3 elements per gene), highly active CRISPRi sgRNA library. Next, we compare CRISPRi effectors to show that the recently published Zim3-dCas9 provides an excellent balance between strong on-target knockdown and minimal non-specific effects on cell growth or the transcriptome. Finally, we engineer a suite of cell lines with stable expression of Zim3-dCas9 and robust on-target knockdown. Our results and publicly available reagents establish best practices for CRISPRi genetic screening.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2050-084X
Relation: https://elifesciences.org/articles/81856; https://doaj.org/toc/2050-084X
DOI: 10.7554/eLife.81856
Access URL: https://doaj.org/article/af03cd98b4f34c128b98cd963fa2ba56
Accession Number: edsdoj.f03cd98b4f34c128b98cd963fa2ba56
Database: Directory of Open Access Journals
More Details
ISSN:2050084X
DOI:10.7554/eLife.81856
Published in:eLife
Language:English