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Quality assessment and control of tissue specific RNA-seq libraries of Drosophila transgenic RNAi models

RNA-sequencing (RNA-seq) is rapidly emerging as the technology of choice for whole-transcriptome studies. However, RNA-seq is not a bias free technique. It requires large amounts of RNA and library preparation can introduce multiple artifacts, compounded by problems from later stages in the process....

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Autores principales: Amaral, Andreia J., Brito, Francisco F., Chobanyan, Tamar, Yoshikawa, Seiko, Yokokura, Takakazu, Van Vactor, David, Gama-Carvalho, Margarida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942661/
https://www.ncbi.nlm.nih.gov/pubmed/24634674
http://dx.doi.org/10.3389/fgene.2014.00043
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author Amaral, Andreia J.
Brito, Francisco F.
Chobanyan, Tamar
Yoshikawa, Seiko
Yokokura, Takakazu
Van Vactor, David
Gama-Carvalho, Margarida
author_facet Amaral, Andreia J.
Brito, Francisco F.
Chobanyan, Tamar
Yoshikawa, Seiko
Yokokura, Takakazu
Van Vactor, David
Gama-Carvalho, Margarida
author_sort Amaral, Andreia J.
collection PubMed
description RNA-sequencing (RNA-seq) is rapidly emerging as the technology of choice for whole-transcriptome studies. However, RNA-seq is not a bias free technique. It requires large amounts of RNA and library preparation can introduce multiple artifacts, compounded by problems from later stages in the process. Nevertheless, RNA-seq is increasingly used in multiple studies, including the characterization of tissue-specific transcriptomes from invertebrate models of human disease. The generation of samples in this context is complex, involving the establishment of mutant strains and the delicate contamination prone process of dissecting the target tissue. Moreover, in order to achieve the required amount of RNA, multiple samples need to be pooled. Such datasets pose extra challenges due to the large variability that may occur between similar pools, mostly due to the presence of cells from surrounding tissues. Therefore, in addition to standard quality control of RNA-seq data, analytical procedures for control of “biological quality” are critical for successful comparison of gene expression profiles. In this study, the transcriptome of the central nervous system (CNS) of a Drosophila transgenic strain with neuronal-specific RNAi of an ubiquitous gene was profiled using RNA-seq. After observing the existence of an unusual variance in our dataset, we showed that the expression profile of a small panel of marker genes, including GAL4 under control of a tissue specific driver, can identify libraries with low levels of contamination from neighboring tissues, enabling the selection of a robust dataset for differential expression analysis. We further analyzed the potential of profiling a complex tissue to identify cell-type specific changes in response to target gene down-regulation. Finally, we showed that trimming 5′ ends of reads decreases nucleotide frequency biases, increasing the coverage of protein coding genes with a potential positive impact in the incurrence of systematic technical errors.
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spelling pubmed-39426612014-03-14 Quality assessment and control of tissue specific RNA-seq libraries of Drosophila transgenic RNAi models Amaral, Andreia J. Brito, Francisco F. Chobanyan, Tamar Yoshikawa, Seiko Yokokura, Takakazu Van Vactor, David Gama-Carvalho, Margarida Front Genet Genetics RNA-sequencing (RNA-seq) is rapidly emerging as the technology of choice for whole-transcriptome studies. However, RNA-seq is not a bias free technique. It requires large amounts of RNA and library preparation can introduce multiple artifacts, compounded by problems from later stages in the process. Nevertheless, RNA-seq is increasingly used in multiple studies, including the characterization of tissue-specific transcriptomes from invertebrate models of human disease. The generation of samples in this context is complex, involving the establishment of mutant strains and the delicate contamination prone process of dissecting the target tissue. Moreover, in order to achieve the required amount of RNA, multiple samples need to be pooled. Such datasets pose extra challenges due to the large variability that may occur between similar pools, mostly due to the presence of cells from surrounding tissues. Therefore, in addition to standard quality control of RNA-seq data, analytical procedures for control of “biological quality” are critical for successful comparison of gene expression profiles. In this study, the transcriptome of the central nervous system (CNS) of a Drosophila transgenic strain with neuronal-specific RNAi of an ubiquitous gene was profiled using RNA-seq. After observing the existence of an unusual variance in our dataset, we showed that the expression profile of a small panel of marker genes, including GAL4 under control of a tissue specific driver, can identify libraries with low levels of contamination from neighboring tissues, enabling the selection of a robust dataset for differential expression analysis. We further analyzed the potential of profiling a complex tissue to identify cell-type specific changes in response to target gene down-regulation. Finally, we showed that trimming 5′ ends of reads decreases nucleotide frequency biases, increasing the coverage of protein coding genes with a potential positive impact in the incurrence of systematic technical errors. Frontiers Media S.A. 2014-03-05 /pmc/articles/PMC3942661/ /pubmed/24634674 http://dx.doi.org/10.3389/fgene.2014.00043 Text en Copyright © 2014 Amaral, Brito, Chobanyan, Yoshikawa, Yokokura, Van Vactor and Gama-Carvalho. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Amaral, Andreia J.
Brito, Francisco F.
Chobanyan, Tamar
Yoshikawa, Seiko
Yokokura, Takakazu
Van Vactor, David
Gama-Carvalho, Margarida
Quality assessment and control of tissue specific RNA-seq libraries of Drosophila transgenic RNAi models
title Quality assessment and control of tissue specific RNA-seq libraries of Drosophila transgenic RNAi models
title_full Quality assessment and control of tissue specific RNA-seq libraries of Drosophila transgenic RNAi models
title_fullStr Quality assessment and control of tissue specific RNA-seq libraries of Drosophila transgenic RNAi models
title_full_unstemmed Quality assessment and control of tissue specific RNA-seq libraries of Drosophila transgenic RNAi models
title_short Quality assessment and control of tissue specific RNA-seq libraries of Drosophila transgenic RNAi models
title_sort quality assessment and control of tissue specific rna-seq libraries of drosophila transgenic rnai models
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942661/
https://www.ncbi.nlm.nih.gov/pubmed/24634674
http://dx.doi.org/10.3389/fgene.2014.00043
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