| Literature DB >> 25502887 |
Lucy Glover1, Sam Alsford2, Nicola Baker1, Daniel J Turner3, Alejandro Sanchez-Flores4, Sebastian Hutchinson1, Christiane Hertz-Fowler5, Matthew Berriman6, David Horn1.
Abstract
The ability to simultaneously assess every gene in a genome for a role in a particular process has obvious appeal. This protocol describes how to perform genome-scale RNAi library screens in bloodstream-form African trypanosomes, a family of parasites that causes lethal human and animal diseases and also serves as a model for studies on basic aspects of eukaryotic biology and evolution. We discuss strain assembly, screen design and implementation, the RNAi target sequencing approach and hit validation, and we provide a step-by-step protocol. A screen can yield from one to thousands of 'hits' associated with the phenotype of interest. The screening protocol itself takes 2 weeks or less to be completed, and high-throughput sequencing may also be completed within weeks. Pre- and post-screen strain assembly, validation and follow-up can take several months, depending on the type of screen and the number of hits analyzed.Entities:
Mesh:
Year: 2014 PMID: 25502887 DOI: 10.1038/nprot.2015.005
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 13.491