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Using genomic DNA-based probe-selection to improve the sensitivity of high-density oligonucleotide arrays when applied to heterologous species
High-density oligonucleotide (oligo) arrays are a powerful tool for transcript profiling. Arrays based on GeneChip(® )technology are amongst the most widely used, although GeneChip(® )arrays are currently available for only a small number of plant and animal species. Thus, we have developed a method...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1308859/ https://www.ncbi.nlm.nih.gov/pubmed/16280083 http://dx.doi.org/10.1186/1746-4811-1-10 |
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author | Hammond, John P Broadley, Martin R Craigon, David J Higgins, Janet Emmerson, Zoe F Townsend, Henrik J White, Philip J May, Sean T |
author_facet | Hammond, John P Broadley, Martin R Craigon, David J Higgins, Janet Emmerson, Zoe F Townsend, Henrik J White, Philip J May, Sean T |
author_sort | Hammond, John P |
collection | PubMed |
description | High-density oligonucleotide (oligo) arrays are a powerful tool for transcript profiling. Arrays based on GeneChip(® )technology are amongst the most widely used, although GeneChip(® )arrays are currently available for only a small number of plant and animal species. Thus, we have developed a method to improve the sensitivity of high-density oligonucleotide arrays when applied to heterologous species and tested the method by analysing the transcriptome of Brassica oleracea L., a species for which no GeneChip(® )array is available, using a GeneChip(® )array designed for Arabidopsis thaliana (L.) Heynh. Genomic DNA from B. oleracea was labelled and hybridised to the ATH1-121501 GeneChip(® )array. Arabidopsis thaliana probe-pairs that hybridised to the B. oleracea genomic DNA on the basis of the perfect-match (PM) probe signal were then selected for subsequent B. oleracea transcriptome analysis using a .cel file parser script to generate probe mask files. The transcriptional response of B. oleracea to a mineral nutrient (phosphorus; P) stress was quantified using probe mask files generated for a wide range of gDNA hybridisation intensity thresholds. An example probe mask file generated with a gDNA hybridisation intensity threshold of 400 removed > 68 % of the available PM probes from the analysis but retained >96 % of available A. thaliana probe-sets. Ninety-nine of these genes were then identified as significantly regulated under P stress in B. oleracea, including the homologues of P stress responsive genes in A. thaliana. Increasing the gDNA hybridisation intensity thresholds up to 500 for probe-selection increased the sensitivity of the GeneChip(® )array to detect regulation of gene expression in B. oleracea under P stress by up to 13-fold. Our open-source software to create probe mask files is freely available and may be used to facilitate transcriptomic analyses of a wide range of plant and animal species in the absence of custom arrays. |
format | Text |
id | pubmed-1308859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-13088592005-12-08 Using genomic DNA-based probe-selection to improve the sensitivity of high-density oligonucleotide arrays when applied to heterologous species Hammond, John P Broadley, Martin R Craigon, David J Higgins, Janet Emmerson, Zoe F Townsend, Henrik J White, Philip J May, Sean T Plant Methods Methodology High-density oligonucleotide (oligo) arrays are a powerful tool for transcript profiling. Arrays based on GeneChip(® )technology are amongst the most widely used, although GeneChip(® )arrays are currently available for only a small number of plant and animal species. Thus, we have developed a method to improve the sensitivity of high-density oligonucleotide arrays when applied to heterologous species and tested the method by analysing the transcriptome of Brassica oleracea L., a species for which no GeneChip(® )array is available, using a GeneChip(® )array designed for Arabidopsis thaliana (L.) Heynh. Genomic DNA from B. oleracea was labelled and hybridised to the ATH1-121501 GeneChip(® )array. Arabidopsis thaliana probe-pairs that hybridised to the B. oleracea genomic DNA on the basis of the perfect-match (PM) probe signal were then selected for subsequent B. oleracea transcriptome analysis using a .cel file parser script to generate probe mask files. The transcriptional response of B. oleracea to a mineral nutrient (phosphorus; P) stress was quantified using probe mask files generated for a wide range of gDNA hybridisation intensity thresholds. An example probe mask file generated with a gDNA hybridisation intensity threshold of 400 removed > 68 % of the available PM probes from the analysis but retained >96 % of available A. thaliana probe-sets. Ninety-nine of these genes were then identified as significantly regulated under P stress in B. oleracea, including the homologues of P stress responsive genes in A. thaliana. Increasing the gDNA hybridisation intensity thresholds up to 500 for probe-selection increased the sensitivity of the GeneChip(® )array to detect regulation of gene expression in B. oleracea under P stress by up to 13-fold. Our open-source software to create probe mask files is freely available and may be used to facilitate transcriptomic analyses of a wide range of plant and animal species in the absence of custom arrays. BioMed Central 2005-11-09 /pmc/articles/PMC1308859/ /pubmed/16280083 http://dx.doi.org/10.1186/1746-4811-1-10 Text en Copyright © 2005 Hammond 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 Hammond, John P Broadley, Martin R Craigon, David J Higgins, Janet Emmerson, Zoe F Townsend, Henrik J White, Philip J May, Sean T Using genomic DNA-based probe-selection to improve the sensitivity of high-density oligonucleotide arrays when applied to heterologous species |
title | Using genomic DNA-based probe-selection to improve the sensitivity of high-density oligonucleotide arrays when applied to heterologous species |
title_full | Using genomic DNA-based probe-selection to improve the sensitivity of high-density oligonucleotide arrays when applied to heterologous species |
title_fullStr | Using genomic DNA-based probe-selection to improve the sensitivity of high-density oligonucleotide arrays when applied to heterologous species |
title_full_unstemmed | Using genomic DNA-based probe-selection to improve the sensitivity of high-density oligonucleotide arrays when applied to heterologous species |
title_short | Using genomic DNA-based probe-selection to improve the sensitivity of high-density oligonucleotide arrays when applied to heterologous species |
title_sort | using genomic dna-based probe-selection to improve the sensitivity of high-density oligonucleotide arrays when applied to heterologous species |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1308859/ https://www.ncbi.nlm.nih.gov/pubmed/16280083 http://dx.doi.org/10.1186/1746-4811-1-10 |
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