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

BACKGROUND: 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 gene...

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Autores principales: Fisher, Katherine H, Wright, Victoria M, Taylor, Amy, Zeidler, Martin P, Brown, Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526451/
https://www.ncbi.nlm.nih.gov/pubmed/23006893
http://dx.doi.org/10.1186/1471-2164-13-506
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author Fisher, Katherine H
Wright, Victoria M
Taylor, Amy
Zeidler, Martin P
Brown, Stephen
author_facet Fisher, Katherine H
Wright, Victoria M
Taylor, Amy
Zeidler, Martin P
Brown, Stephen
author_sort Fisher, Katherine H
collection PubMed
description BACKGROUND: 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. RESULTS: Here we present a new genome-wide RNAi screen of the Drosophila 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. CONCLUSIONS: 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.
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spelling pubmed-35264512012-12-20 Advances in genome-wide RNAi cellular screens: a case study using the Drosophila JAK/STAT pathway Fisher, Katherine H Wright, Victoria M Taylor, Amy Zeidler, Martin P Brown, Stephen BMC Genomics Research Article BACKGROUND: 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. RESULTS: Here we present a new genome-wide RNAi screen of the Drosophila 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. CONCLUSIONS: 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. BioMed Central 2012-09-24 /pmc/articles/PMC3526451/ /pubmed/23006893 http://dx.doi.org/10.1186/1471-2164-13-506 Text en Copyright ©2012 Fisher et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
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 Drosophila JAK/STAT pathway
title Advances in genome-wide RNAi cellular screens: a case study using the Drosophila JAK/STAT pathway
title_full Advances in genome-wide RNAi cellular screens: a case study using the Drosophila JAK/STAT pathway
title_fullStr Advances in genome-wide RNAi cellular screens: a case study using the Drosophila JAK/STAT pathway
title_full_unstemmed Advances in genome-wide RNAi cellular screens: a case study using the Drosophila JAK/STAT pathway
title_short Advances in genome-wide RNAi cellular screens: a case study using the Drosophila JAK/STAT pathway
title_sort advances in genome-wide rnai cellular screens: a case study using the drosophila jak/stat pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526451/
https://www.ncbi.nlm.nih.gov/pubmed/23006893
http://dx.doi.org/10.1186/1471-2164-13-506
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