| Literature DB >> 27795562 |
Benjamin E Housden1, Matthias Muhar2, Matthew Gemberling3, Charles A Gersbach3, Didier Y R Stainier4, Geraldine Seydoux5,6, Stephanie E Mohr1, Johannes Zuber2, Norbert Perrimon1,7.
Abstract
Our understanding of the genetic mechanisms that underlie biological processes has relied extensively on loss-of-function (LOF) analyses. LOF methods target DNA, RNA or protein to reduce or to ablate gene function. By analysing the phenotypes that are caused by these perturbations the wild-type function of genes can be elucidated. Although all LOF methods reduce gene activity, the choice of approach (for example, mutagenesis, CRISPR-based gene editing, RNA interference, morpholinos or pharmacological inhibition) can have a major effect on phenotypic outcomes. Interpretation of the LOF phenotype must take into account the biological process that is targeted by each method. The practicality and efficiency of LOF methods also vary considerably between model systems. We describe parameters for choosing the optimal combination of method and system, and for interpreting phenotypes within the constraints of each method.Entities:
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Year: 2016 PMID: 27795562 PMCID: PMC5206767 DOI: 10.1038/nrg.2016.118
Source DB: PubMed Journal: Nat Rev Genet ISSN: 1471-0056 Impact factor: 53.242