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Utilization of a labeled tracking oligonucleotide for visualization and quality control of spotted 70-mer arrays

BACKGROUND: Spotted 70-mer oligonucleotide arrays offer potentially greater specificity and an alternative to expensive cDNA library maintenance and amplification. Since microarray fabrication is a considerable source of data variance, we previously directly tagged cDNA probes with a third fluoropho...

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Autores principales: Hessner, Martin J, Singh, Vineet K, Wang, Xujing, Khan, Shehnaz, Tschannen, Michael R, Zahrt, Thomas C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC362869/
https://www.ncbi.nlm.nih.gov/pubmed/15018646
http://dx.doi.org/10.1186/1471-2164-5-12
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author Hessner, Martin J
Singh, Vineet K
Wang, Xujing
Khan, Shehnaz
Tschannen, Michael R
Zahrt, Thomas C
author_facet Hessner, Martin J
Singh, Vineet K
Wang, Xujing
Khan, Shehnaz
Tschannen, Michael R
Zahrt, Thomas C
author_sort Hessner, Martin J
collection PubMed
description BACKGROUND: Spotted 70-mer oligonucleotide arrays offer potentially greater specificity and an alternative to expensive cDNA library maintenance and amplification. Since microarray fabrication is a considerable source of data variance, we previously directly tagged cDNA probes with a third fluorophore for prehybridization quality control. Fluorescently modifying oligonucleotide sets is cost prohibitive, therefore, a co-spotted Staphylococcus aureus-specific fluorescein-labeled "tracking" oligonucleotide is described to monitor fabrication variables of a Mycobacterium tuberculosis oligonucleotide microarray. RESULTS: Significantly (p < 0.01) improved DNA retention was achieved printing in 15% DMSO/1.5 M betaine compared to the vendor recommended buffers. Introduction of tracking oligonucleotide did not effect hybridization efficiency or introduce ratio measurement bias in hybridizations between M. tuberculosis H37Rv and M. tuberculosis mprA. Linearity between the mean log Cy3/Cy5 ratios of genes differentially expressed from arrays either possessing or lacking the tracking oligonucleotide was observed (R(2 )= 0.90, p < 0.05) and there were no significant differences in Pearson's correlation coefficients of ratio data between replicates possessing (0.72 ± 0.07), replicates lacking (0.74 ± 0.10), or replicates with and without (0.70 ± 0.04) the tracking oligonucleotide. ANOVA analysis confirmed the tracking oligonucleotide introduced no bias. Titrating target-specific oligonucleotide (40 μM to 0.78 μM) in the presence of 0.5 μM tracking oligonucleotide, revealed a fluorescein fluorescence inversely related to target-specific oligonucleotide molarity, making tracking oligonucleotide signal useful for quality control measurements and differentiating false negatives (synthesis failures and mechanical misses) from true negatives (no gene expression). CONCLUSIONS: This novel approach enables prehybridization array visualization for spotted oligonucleotide arrays and sets the stage for more sophisticated slide qualification and data filtering applications.
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spelling pubmed-3628692004-03-11 Utilization of a labeled tracking oligonucleotide for visualization and quality control of spotted 70-mer arrays Hessner, Martin J Singh, Vineet K Wang, Xujing Khan, Shehnaz Tschannen, Michael R Zahrt, Thomas C BMC Genomics Methodology Article BACKGROUND: Spotted 70-mer oligonucleotide arrays offer potentially greater specificity and an alternative to expensive cDNA library maintenance and amplification. Since microarray fabrication is a considerable source of data variance, we previously directly tagged cDNA probes with a third fluorophore for prehybridization quality control. Fluorescently modifying oligonucleotide sets is cost prohibitive, therefore, a co-spotted Staphylococcus aureus-specific fluorescein-labeled "tracking" oligonucleotide is described to monitor fabrication variables of a Mycobacterium tuberculosis oligonucleotide microarray. RESULTS: Significantly (p < 0.01) improved DNA retention was achieved printing in 15% DMSO/1.5 M betaine compared to the vendor recommended buffers. Introduction of tracking oligonucleotide did not effect hybridization efficiency or introduce ratio measurement bias in hybridizations between M. tuberculosis H37Rv and M. tuberculosis mprA. Linearity between the mean log Cy3/Cy5 ratios of genes differentially expressed from arrays either possessing or lacking the tracking oligonucleotide was observed (R(2 )= 0.90, p < 0.05) and there were no significant differences in Pearson's correlation coefficients of ratio data between replicates possessing (0.72 ± 0.07), replicates lacking (0.74 ± 0.10), or replicates with and without (0.70 ± 0.04) the tracking oligonucleotide. ANOVA analysis confirmed the tracking oligonucleotide introduced no bias. Titrating target-specific oligonucleotide (40 μM to 0.78 μM) in the presence of 0.5 μM tracking oligonucleotide, revealed a fluorescein fluorescence inversely related to target-specific oligonucleotide molarity, making tracking oligonucleotide signal useful for quality control measurements and differentiating false negatives (synthesis failures and mechanical misses) from true negatives (no gene expression). CONCLUSIONS: This novel approach enables prehybridization array visualization for spotted oligonucleotide arrays and sets the stage for more sophisticated slide qualification and data filtering applications. BioMed Central 2004-02-09 /pmc/articles/PMC362869/ /pubmed/15018646 http://dx.doi.org/10.1186/1471-2164-5-12 Text en Copyright © 2004 Hessner et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Methodology Article
Hessner, Martin J
Singh, Vineet K
Wang, Xujing
Khan, Shehnaz
Tschannen, Michael R
Zahrt, Thomas C
Utilization of a labeled tracking oligonucleotide for visualization and quality control of spotted 70-mer arrays
title Utilization of a labeled tracking oligonucleotide for visualization and quality control of spotted 70-mer arrays
title_full Utilization of a labeled tracking oligonucleotide for visualization and quality control of spotted 70-mer arrays
title_fullStr Utilization of a labeled tracking oligonucleotide for visualization and quality control of spotted 70-mer arrays
title_full_unstemmed Utilization of a labeled tracking oligonucleotide for visualization and quality control of spotted 70-mer arrays
title_short Utilization of a labeled tracking oligonucleotide for visualization and quality control of spotted 70-mer arrays
title_sort utilization of a labeled tracking oligonucleotide for visualization and quality control of spotted 70-mer arrays
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC362869/
https://www.ncbi.nlm.nih.gov/pubmed/15018646
http://dx.doi.org/10.1186/1471-2164-5-12
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