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Pooled RNAi Screens - Technical and Biological Aspects

RNA interference (RNAi) screens have recently emerged as an exciting new tool for studying gene function in mammalian cells. In order to facilitate those studies, short hairpin RNA (shRNA) expression libraries covering the entire human transcriptome have become commercially available. To make use of...

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Detalles Bibliográficos
Autores principales: Boettcher, M., Hoheisel, J.D.
Formato: Texto
Lenguaje:English
Publicado: Bentham Science Publishers Ltd. 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2878981/
https://www.ncbi.nlm.nih.gov/pubmed/21037854
http://dx.doi.org/10.2174/138920210791110988
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author Boettcher, M.
Hoheisel, J.D.
author_facet Boettcher, M.
Hoheisel, J.D.
author_sort Boettcher, M.
collection PubMed
description RNA interference (RNAi) screens have recently emerged as an exciting new tool for studying gene function in mammalian cells. In order to facilitate those studies, short hairpin RNA (shRNA) expression libraries covering the entire human transcriptome have become commercially available. To make use of the full potential of such large-scale shRNA libraries, microarray-based methods have been developed to analyze complex pooled RNAi screens. In terms of microarray analysis, different strategies have been pursued by different research groups, largely influenced by the employed shRNA library. In this review, we compare the three major shRNA expression libraries with a focus on their suitability for a microarray-based analysis of pooled screens. We analyze and compare approaches previously used to perform pooled RNAi screens and point out their advantages as well as limitations.
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spelling pubmed-28789812010-11-01 Pooled RNAi Screens - Technical and Biological Aspects Boettcher, M. Hoheisel, J.D. Curr Genomics Article RNA interference (RNAi) screens have recently emerged as an exciting new tool for studying gene function in mammalian cells. In order to facilitate those studies, short hairpin RNA (shRNA) expression libraries covering the entire human transcriptome have become commercially available. To make use of the full potential of such large-scale shRNA libraries, microarray-based methods have been developed to analyze complex pooled RNAi screens. In terms of microarray analysis, different strategies have been pursued by different research groups, largely influenced by the employed shRNA library. In this review, we compare the three major shRNA expression libraries with a focus on their suitability for a microarray-based analysis of pooled screens. We analyze and compare approaches previously used to perform pooled RNAi screens and point out their advantages as well as limitations. Bentham Science Publishers Ltd. 2010-05 /pmc/articles/PMC2878981/ /pubmed/21037854 http://dx.doi.org/10.2174/138920210791110988 Text en ©2010 Bentham Science Publishers Ltd. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestrictive use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Boettcher, M.
Hoheisel, J.D.
Pooled RNAi Screens - Technical and Biological Aspects
title Pooled RNAi Screens - Technical and Biological Aspects
title_full Pooled RNAi Screens - Technical and Biological Aspects
title_fullStr Pooled RNAi Screens - Technical and Biological Aspects
title_full_unstemmed Pooled RNAi Screens - Technical and Biological Aspects
title_short Pooled RNAi Screens - Technical and Biological Aspects
title_sort pooled rnai screens - technical and biological aspects
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2878981/
https://www.ncbi.nlm.nih.gov/pubmed/21037854
http://dx.doi.org/10.2174/138920210791110988
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