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Automated Workflow for Preparation of cDNA for Cap Analysis of Gene Expression on a Single Molecule Sequencer

BACKGROUND: Cap analysis of gene expression (CAGE) is a 5′ sequence tag technology to globally determine transcriptional starting sites in the genome and their expression levels and has most recently been adapted to the HeliScope single molecule sequencer. Despite significant simplifications in the...

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Autores principales: Itoh, Masayoshi, Kojima, Miki, Nagao-Sato, Sayaka, Saijo, Eri, Lassmann, Timo, Kanamori-Katayama, Mutsumi, Kaiho, Ai, Lizio, Marina, Kawaji, Hideya, Carninci, Piero, Forrest, Alistair R. R., Hayashizaki, Yoshihide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268765/
https://www.ncbi.nlm.nih.gov/pubmed/22303458
http://dx.doi.org/10.1371/journal.pone.0030809
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author Itoh, Masayoshi
Kojima, Miki
Nagao-Sato, Sayaka
Saijo, Eri
Lassmann, Timo
Kanamori-Katayama, Mutsumi
Kaiho, Ai
Lizio, Marina
Kawaji, Hideya
Carninci, Piero
Forrest, Alistair R. R.
Hayashizaki, Yoshihide
author_facet Itoh, Masayoshi
Kojima, Miki
Nagao-Sato, Sayaka
Saijo, Eri
Lassmann, Timo
Kanamori-Katayama, Mutsumi
Kaiho, Ai
Lizio, Marina
Kawaji, Hideya
Carninci, Piero
Forrest, Alistair R. R.
Hayashizaki, Yoshihide
author_sort Itoh, Masayoshi
collection PubMed
description BACKGROUND: Cap analysis of gene expression (CAGE) is a 5′ sequence tag technology to globally determine transcriptional starting sites in the genome and their expression levels and has most recently been adapted to the HeliScope single molecule sequencer. Despite significant simplifications in the CAGE protocol, it has until now been a labour intensive protocol. METHODOLOGY: In this study we set out to adapt the protocol to a robotic workflow, which would increase throughput and reduce handling. The automated CAGE cDNA preparation system we present here can prepare 96 ‘HeliScope ready’ CAGE cDNA libraries in 8 days, as opposed to 6 weeks by a manual operator.We compare the results obtained using the same RNA in manual libraries and across multiple automation batches to assess reproducibility. CONCLUSIONS: We show that the sequencing was highly reproducible and comparable to manual libraries with an 8 fold increase in productivity. The automated CAGE cDNA preparation system can prepare 96 CAGE sequencing samples simultaneously. Finally we discuss how the system could be used for CAGE on Illumina/SOLiD platforms, RNA-seq and full-length cDNA generation.
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spelling pubmed-32687652012-02-02 Automated Workflow for Preparation of cDNA for Cap Analysis of Gene Expression on a Single Molecule Sequencer Itoh, Masayoshi Kojima, Miki Nagao-Sato, Sayaka Saijo, Eri Lassmann, Timo Kanamori-Katayama, Mutsumi Kaiho, Ai Lizio, Marina Kawaji, Hideya Carninci, Piero Forrest, Alistair R. R. Hayashizaki, Yoshihide PLoS One Research Article BACKGROUND: Cap analysis of gene expression (CAGE) is a 5′ sequence tag technology to globally determine transcriptional starting sites in the genome and their expression levels and has most recently been adapted to the HeliScope single molecule sequencer. Despite significant simplifications in the CAGE protocol, it has until now been a labour intensive protocol. METHODOLOGY: In this study we set out to adapt the protocol to a robotic workflow, which would increase throughput and reduce handling. The automated CAGE cDNA preparation system we present here can prepare 96 ‘HeliScope ready’ CAGE cDNA libraries in 8 days, as opposed to 6 weeks by a manual operator.We compare the results obtained using the same RNA in manual libraries and across multiple automation batches to assess reproducibility. CONCLUSIONS: We show that the sequencing was highly reproducible and comparable to manual libraries with an 8 fold increase in productivity. The automated CAGE cDNA preparation system can prepare 96 CAGE sequencing samples simultaneously. Finally we discuss how the system could be used for CAGE on Illumina/SOLiD platforms, RNA-seq and full-length cDNA generation. Public Library of Science 2012-01-30 /pmc/articles/PMC3268765/ /pubmed/22303458 http://dx.doi.org/10.1371/journal.pone.0030809 Text en Itoh et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Itoh, Masayoshi
Kojima, Miki
Nagao-Sato, Sayaka
Saijo, Eri
Lassmann, Timo
Kanamori-Katayama, Mutsumi
Kaiho, Ai
Lizio, Marina
Kawaji, Hideya
Carninci, Piero
Forrest, Alistair R. R.
Hayashizaki, Yoshihide
Automated Workflow for Preparation of cDNA for Cap Analysis of Gene Expression on a Single Molecule Sequencer
title Automated Workflow for Preparation of cDNA for Cap Analysis of Gene Expression on a Single Molecule Sequencer
title_full Automated Workflow for Preparation of cDNA for Cap Analysis of Gene Expression on a Single Molecule Sequencer
title_fullStr Automated Workflow for Preparation of cDNA for Cap Analysis of Gene Expression on a Single Molecule Sequencer
title_full_unstemmed Automated Workflow for Preparation of cDNA for Cap Analysis of Gene Expression on a Single Molecule Sequencer
title_short Automated Workflow for Preparation of cDNA for Cap Analysis of Gene Expression on a Single Molecule Sequencer
title_sort automated workflow for preparation of cdna for cap analysis of gene expression on a single molecule sequencer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268765/
https://www.ncbi.nlm.nih.gov/pubmed/22303458
http://dx.doi.org/10.1371/journal.pone.0030809
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