Advances in genome-wide RNAi cellular screens: a case study using the <it>Drosophila</it> JAK/STAT pathway

<p>Abstract</p> <p>Background</p> <p>Genome-scale RNA-interference (RNAi) screens are becoming ever more common gene discovery tools. However, whilst every screen identifies interacting genes, less attention has been given to how factors such as library design and post-...

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Main Authors: Fisher Katherine H, Wright Victoria M, Taylor Amy, Zeidler Martin P, Brown Stephen
Format: Article
Language:English
Published: BMC 2012-09-01
Series:BMC Genomics
Subjects:
Online Access:http://www.biomedcentral.com/1471-2164/13/506
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spelling doaj-663ac7c5067248ab856dc9d91b55dbe82020-11-24T20:49:50ZengBMCBMC Genomics1471-21642012-09-0113150610.1186/1471-2164-13-506Advances in genome-wide RNAi cellular screens: a case study using the <it>Drosophila</it> JAK/STAT pathwayFisher Katherine HWright Victoria MTaylor AmyZeidler Martin PBrown Stephen<p>Abstract</p> <p>Background</p> <p>Genome-scale RNA-interference (RNAi) screens are becoming ever more common gene discovery tools. However, whilst every screen identifies interacting genes, less attention has been given to how factors such as library design and post-screening bioinformatics may be effecting the data generated.</p> <p>Results</p> <p>Here we present a new genome-wide RNAi screen of the <it>Drosophila</it> JAK/STAT signalling pathway undertaken in the Sheffield RNAi Screening Facility (SRSF). This screen was carried out using a second-generation, computationally optimised dsRNA library and analysed using current methods and bioinformatic tools. To examine advances in RNAi screening technology, we compare this screen to a biologically very similar screen undertaken in 2005 with a first-generation library. Both screens used the same cell line, reporters and experimental design, with the SRSF screen identifying 42 putative regulators of JAK/STAT signalling, 22 of which verified in a secondary screen and 16 verified with an independent probe design. Following reanalysis of the original screen data, comparisons of the two gene lists allows us to make estimates of false discovery rates in the SRSF data and to conduct an assessment of off-target effects (OTEs) associated with both libraries. We discuss the differences and similarities between the resulting data sets and examine the relative improvements in gene discovery protocols.</p> <p>Conclusions</p> <p>Our work represents one of the first direct comparisons between first- and second-generation libraries and shows that modern library designs together with methodological advances have had a significant influence on genome-scale RNAi screens.</p> http://www.biomedcentral.com/1471-2164/13/506Genome screeningRNAiOff-target effectJAK/STAT pathwayFunctional genomicsdsRNA
collection DOAJ
language English
format Article
sources DOAJ
author Fisher Katherine H
Wright Victoria M
Taylor Amy
Zeidler Martin P
Brown Stephen
spellingShingle Fisher Katherine H
Wright Victoria M
Taylor Amy
Zeidler Martin P
Brown Stephen
Advances in genome-wide RNAi cellular screens: a case study using the <it>Drosophila</it> JAK/STAT pathway
BMC Genomics
Genome screening
RNAi
Off-target effect
JAK/STAT pathway
Functional genomics
dsRNA
author_facet Fisher Katherine H
Wright Victoria M
Taylor Amy
Zeidler Martin P
Brown Stephen
author_sort Fisher Katherine H
title Advances in genome-wide RNAi cellular screens: a case study using the <it>Drosophila</it> JAK/STAT pathway
title_short Advances in genome-wide RNAi cellular screens: a case study using the <it>Drosophila</it> JAK/STAT pathway
title_full Advances in genome-wide RNAi cellular screens: a case study using the <it>Drosophila</it> JAK/STAT pathway
title_fullStr Advances in genome-wide RNAi cellular screens: a case study using the <it>Drosophila</it> JAK/STAT pathway
title_full_unstemmed Advances in genome-wide RNAi cellular screens: a case study using the <it>Drosophila</it> JAK/STAT pathway
title_sort advances in genome-wide rnai cellular screens: a case study using the <it>drosophila</it> jak/stat pathway
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2012-09-01
description <p>Abstract</p> <p>Background</p> <p>Genome-scale RNA-interference (RNAi) screens are becoming ever more common gene discovery tools. However, whilst every screen identifies interacting genes, less attention has been given to how factors such as library design and post-screening bioinformatics may be effecting the data generated.</p> <p>Results</p> <p>Here we present a new genome-wide RNAi screen of the <it>Drosophila</it> JAK/STAT signalling pathway undertaken in the Sheffield RNAi Screening Facility (SRSF). This screen was carried out using a second-generation, computationally optimised dsRNA library and analysed using current methods and bioinformatic tools. To examine advances in RNAi screening technology, we compare this screen to a biologically very similar screen undertaken in 2005 with a first-generation library. Both screens used the same cell line, reporters and experimental design, with the SRSF screen identifying 42 putative regulators of JAK/STAT signalling, 22 of which verified in a secondary screen and 16 verified with an independent probe design. Following reanalysis of the original screen data, comparisons of the two gene lists allows us to make estimates of false discovery rates in the SRSF data and to conduct an assessment of off-target effects (OTEs) associated with both libraries. We discuss the differences and similarities between the resulting data sets and examine the relative improvements in gene discovery protocols.</p> <p>Conclusions</p> <p>Our work represents one of the first direct comparisons between first- and second-generation libraries and shows that modern library designs together with methodological advances have had a significant influence on genome-scale RNAi screens.</p>
topic Genome screening
RNAi
Off-target effect
JAK/STAT pathway
Functional genomics
dsRNA
url http://www.biomedcentral.com/1471-2164/13/506
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