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dc.contributor.authorJohn Calarco
dc.contributor.authorAdam Norris
dc.contributor.otherDepartment of Cell and Systems Biology, University of Toronto, Toronto, Canada
dc.contributor.otherDepartment of Biological Sciences, Southern Methodist University, Dallas, United States
dc.date.accessioned2024-06-05T01:57:10Z
dc.date.accessioned2025-10-08T08:47:36Z
dc.date.available2025-10-08T08:47:36Z
dc.date.issued01-03-2018
dc.identifier.urihttp://digilib.fisipol.ugm.ac.id/repo/handle/15717717/37264
dc.description.abstractGenetic interaction screens are a powerful methodology to establish novel roles for genes and elucidate functional connections between genes. Such studies have been performed to great effect in single-cell organisms such as yeast and E. coli (Schuldiner et al., 2005; Butland et al., 2008; Costanzo et al., 2010), but similar large-scale interaction studies using targeted reverse-genetic deletions in multi-cellular organisms have not been feasible. We developed a CRISPR/Cas9-based method for deleting genes in C. elegans and replacing them with a heterologous fluorescent reporter (Norris et al., 2015). Recently we took advantage of that system to perform a large-scale, reverse genetic screen using null alleles in animals for the first time, focusing on RNA binding protein genes (Norris et al., 2017). This type of approach should be similarly applicable to many other gene classes in C. elegans. Here we detail the protocols involved in generating a library of double mutants and performing medium-throughput competitive fitness assays to test for genetic interactions resulting in fitness changes.
dc.language.isoEN
dc.publisherBio-protocol LLC
dc.subject.lccBiology (General)
dc.titleSynthetic Genetic Interaction (CRISPR-SGI) Profiling in Caenorhabditis elegans
dc.typeArticle
dc.description.doi10.21769/BioProtoc.2756
dc.title.journalBio-Protocol
dc.identifier.e-issn2331-8325
dc.identifier.oaioai:doaj.org/journal:82674e3840944e9697bdcedf7345e7e3
dc.journal.infoVolume 8, Issue 5


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