Genome-scale RNAi screens for high-throughput phenotyping in bloodstream-form African trypanosomes

被引:42
作者
Glover, Lucy [1 ]
Alsford, Sam [2 ]
Baker, Nicola [1 ]
Turner, Daniel J. [3 ]
Sanchez-Flores, Alejandro [4 ]
Hutchinson, Sebastian [1 ]
Hertz-Fowler, Christiane [5 ]
Berriman, Matthew [6 ]
Horn, David [1 ]
机构
[1] Univ Dundee, Coll Life Sci, Div Biol Chem & Drug Discovery, Dundee, Scotland
[2] London Sch Hyg & Trop Med, London WC1, England
[3] Oxford Nanopore Technol, Oxford, England
[4] Univ Nacl Autonoma Mexico, Inst Biotechnol, Cuernavaca 62191, Morelos, Mexico
[5] Univ Liverpool, Inst Integrat Biol, Ctr Genom Res, Liverpool L69 3BX, Merseyside, England
[6] Wellcome Trust Sanger Inst, Cambridge, England
基金
英国惠康基金;
关键词
DOUBLE-STRANDED-RNA; GENE-EXPRESSION; INTERFERENCE LIBRARY; BRUCEI; RESISTANCE; EFFICIENCY; PROMOTERS; SUSCEPTIBILITY; TRANSFORMATION; MELARSOPROL;
D O I
10.1038/nprot.2015.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:106 / 133
页数:28
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