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Improved microarray gene expression profiling of virus-infected cells after removal of viral RNA

BACKGROUND: Sensitivity and accuracy are key points when using microarrays to detect alterations in gene expression under different conditions. Critical to the acquisition of reliable results is the preparation of the RNA. In the field of virology, when analyzing the host cell's reaction to inf...

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Autores principales: Raaben, Matthijs, Whitley, Penn, Bouwmeester, Diane, Setterquist, Robert A, Rottier, Peter JM, de Haan, Cornelis AM
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2397413/
https://www.ncbi.nlm.nih.gov/pubmed/18479515
http://dx.doi.org/10.1186/1471-2164-9-221
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author Raaben, Matthijs
Whitley, Penn
Bouwmeester, Diane
Setterquist, Robert A
Rottier, Peter JM
de Haan, Cornelis AM
author_facet Raaben, Matthijs
Whitley, Penn
Bouwmeester, Diane
Setterquist, Robert A
Rottier, Peter JM
de Haan, Cornelis AM
author_sort Raaben, Matthijs
collection PubMed
description BACKGROUND: Sensitivity and accuracy are key points when using microarrays to detect alterations in gene expression under different conditions. Critical to the acquisition of reliable results is the preparation of the RNA. In the field of virology, when analyzing the host cell's reaction to infection, the often high representation of viral RNA (vRNA) within total RNA preparations from infected cells is likely to interfere with microarray analysis. Yet, this effect has not been investigated despite the many reports that describe gene expression profiling of virus-infected cells using microarrays. RESULTS: In this study we used coronaviruses as a model to show that vRNA indeed interferes with microarray analysis, decreasing both sensitivity and accuracy. We also demonstrate that the removal of vRNA from total RNA samples, by means of virus-specific oligonucleotide capturing, significantly reduced the number of false-positive hits and increased the sensitivity of the method as tested on different array platforms. CONCLUSION: We therefore recommend the specific removal of vRNA, or of any other abundant 'contaminating' RNAs, from total RNA samples to improve the quality and reliability of microarray analyses.
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spelling pubmed-23974132008-05-29 Improved microarray gene expression profiling of virus-infected cells after removal of viral RNA Raaben, Matthijs Whitley, Penn Bouwmeester, Diane Setterquist, Robert A Rottier, Peter JM de Haan, Cornelis AM BMC Genomics Methodology Article BACKGROUND: Sensitivity and accuracy are key points when using microarrays to detect alterations in gene expression under different conditions. Critical to the acquisition of reliable results is the preparation of the RNA. In the field of virology, when analyzing the host cell's reaction to infection, the often high representation of viral RNA (vRNA) within total RNA preparations from infected cells is likely to interfere with microarray analysis. Yet, this effect has not been investigated despite the many reports that describe gene expression profiling of virus-infected cells using microarrays. RESULTS: In this study we used coronaviruses as a model to show that vRNA indeed interferes with microarray analysis, decreasing both sensitivity and accuracy. We also demonstrate that the removal of vRNA from total RNA samples, by means of virus-specific oligonucleotide capturing, significantly reduced the number of false-positive hits and increased the sensitivity of the method as tested on different array platforms. CONCLUSION: We therefore recommend the specific removal of vRNA, or of any other abundant 'contaminating' RNAs, from total RNA samples to improve the quality and reliability of microarray analyses. BioMed Central 2008-05-14 /pmc/articles/PMC2397413/ /pubmed/18479515 http://dx.doi.org/10.1186/1471-2164-9-221 Text en Copyright © 2008 Raaben 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 Methodology Article
Raaben, Matthijs
Whitley, Penn
Bouwmeester, Diane
Setterquist, Robert A
Rottier, Peter JM
de Haan, Cornelis AM
Improved microarray gene expression profiling of virus-infected cells after removal of viral RNA
title Improved microarray gene expression profiling of virus-infected cells after removal of viral RNA
title_full Improved microarray gene expression profiling of virus-infected cells after removal of viral RNA
title_fullStr Improved microarray gene expression profiling of virus-infected cells after removal of viral RNA
title_full_unstemmed Improved microarray gene expression profiling of virus-infected cells after removal of viral RNA
title_short Improved microarray gene expression profiling of virus-infected cells after removal of viral RNA
title_sort improved microarray gene expression profiling of virus-infected cells after removal of viral rna
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2397413/
https://www.ncbi.nlm.nih.gov/pubmed/18479515
http://dx.doi.org/10.1186/1471-2164-9-221
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