Cargando…

Replicate high-density rat genome oligonucleotide microarrays reveal hundreds of regulated genes in the dorsal root ganglion after peripheral nerve injury.

BACKGROUND: Rat oligonucleotide microarrays were used to detect changes in gene expression in the dorsal root ganglion (DRG) 3 days following sciatic nerve transection (axotomy). Two comparisons were made using two sets of triplicate microarrays, naïve versus naïve and naïve versus axotomy. RESULTS:...

Descripción completa

Detalles Bibliográficos
Autores principales: Costigan, Michael, Befort, Katia, Karchewski, Laurie, Griffin, Robert S, D'Urso, Donatella, Allchorne, Andrew, Sitarski, Joanne, Mannion, James W, Pratt, Richard E, Woolf, Clifford J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139981/
https://www.ncbi.nlm.nih.gov/pubmed/12401135
http://dx.doi.org/10.1186/1471-2202-3-16
_version_ 1782120582239748096
author Costigan, Michael
Befort, Katia
Karchewski, Laurie
Griffin, Robert S
D'Urso, Donatella
Allchorne, Andrew
Sitarski, Joanne
Mannion, James W
Pratt, Richard E
Woolf, Clifford J
author_facet Costigan, Michael
Befort, Katia
Karchewski, Laurie
Griffin, Robert S
D'Urso, Donatella
Allchorne, Andrew
Sitarski, Joanne
Mannion, James W
Pratt, Richard E
Woolf, Clifford J
author_sort Costigan, Michael
collection PubMed
description BACKGROUND: Rat oligonucleotide microarrays were used to detect changes in gene expression in the dorsal root ganglion (DRG) 3 days following sciatic nerve transection (axotomy). Two comparisons were made using two sets of triplicate microarrays, naïve versus naïve and naïve versus axotomy. RESULTS: Microarray variability was assessed using the naïve versus naïve comparison. These results support use of a P < 0.05 significance threshold for detecting regulated genes, despite the large number of hypothesis tests required. For the naïve versus axotomy comparison, a 2-fold cut off alone led to an estimated error rate of 16%; combining a >1.5-fold expression change and P < 0.05 significance reduced the estimated error to 5%. The 2-fold cut off identified 178 genes while the combined >1.5-fold and P < 0.05 criteria generated 240 putatively regulated genes, which we have listed. Many of these have not been described as regulated in the DRG by axotomy. Northern blot, quantitative slot blots and in situ hybridization verified the expression of 24 transcripts. These data showed an 83% concordance rate with the arrays; most mismatches represent genes with low expression levels reflecting limits of array sensitivity. A significant correlation was found between actual mRNA differences and relative changes between microarrays (r(2 )= 0.8567). Temporal patterns of individual genes regulation varied. CONCLUSIONS: We identify parameters for microarray analysis which reduce error while identifying many putatively regulated genes. Functional classification of these genes suggest reorganization of cell structural components, activation of genes expressed by immune and inflammatory cells and down-regulation of genes involved in neurotransmission.
format Text
id pubmed-139981
institution National Center for Biotechnology Information
language English
publishDate 2002
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-1399812003-01-15 Replicate high-density rat genome oligonucleotide microarrays reveal hundreds of regulated genes in the dorsal root ganglion after peripheral nerve injury. Costigan, Michael Befort, Katia Karchewski, Laurie Griffin, Robert S D'Urso, Donatella Allchorne, Andrew Sitarski, Joanne Mannion, James W Pratt, Richard E Woolf, Clifford J BMC Neurosci Research Article BACKGROUND: Rat oligonucleotide microarrays were used to detect changes in gene expression in the dorsal root ganglion (DRG) 3 days following sciatic nerve transection (axotomy). Two comparisons were made using two sets of triplicate microarrays, naïve versus naïve and naïve versus axotomy. RESULTS: Microarray variability was assessed using the naïve versus naïve comparison. These results support use of a P < 0.05 significance threshold for detecting regulated genes, despite the large number of hypothesis tests required. For the naïve versus axotomy comparison, a 2-fold cut off alone led to an estimated error rate of 16%; combining a >1.5-fold expression change and P < 0.05 significance reduced the estimated error to 5%. The 2-fold cut off identified 178 genes while the combined >1.5-fold and P < 0.05 criteria generated 240 putatively regulated genes, which we have listed. Many of these have not been described as regulated in the DRG by axotomy. Northern blot, quantitative slot blots and in situ hybridization verified the expression of 24 transcripts. These data showed an 83% concordance rate with the arrays; most mismatches represent genes with low expression levels reflecting limits of array sensitivity. A significant correlation was found between actual mRNA differences and relative changes between microarrays (r(2 )= 0.8567). Temporal patterns of individual genes regulation varied. CONCLUSIONS: We identify parameters for microarray analysis which reduce error while identifying many putatively regulated genes. Functional classification of these genes suggest reorganization of cell structural components, activation of genes expressed by immune and inflammatory cells and down-regulation of genes involved in neurotransmission. BioMed Central 2002-10-25 /pmc/articles/PMC139981/ /pubmed/12401135 http://dx.doi.org/10.1186/1471-2202-3-16 Text en Copyright © 2002 Costigan 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 Research Article
Costigan, Michael
Befort, Katia
Karchewski, Laurie
Griffin, Robert S
D'Urso, Donatella
Allchorne, Andrew
Sitarski, Joanne
Mannion, James W
Pratt, Richard E
Woolf, Clifford J
Replicate high-density rat genome oligonucleotide microarrays reveal hundreds of regulated genes in the dorsal root ganglion after peripheral nerve injury.
title Replicate high-density rat genome oligonucleotide microarrays reveal hundreds of regulated genes in the dorsal root ganglion after peripheral nerve injury.
title_full Replicate high-density rat genome oligonucleotide microarrays reveal hundreds of regulated genes in the dorsal root ganglion after peripheral nerve injury.
title_fullStr Replicate high-density rat genome oligonucleotide microarrays reveal hundreds of regulated genes in the dorsal root ganglion after peripheral nerve injury.
title_full_unstemmed Replicate high-density rat genome oligonucleotide microarrays reveal hundreds of regulated genes in the dorsal root ganglion after peripheral nerve injury.
title_short Replicate high-density rat genome oligonucleotide microarrays reveal hundreds of regulated genes in the dorsal root ganglion after peripheral nerve injury.
title_sort replicate high-density rat genome oligonucleotide microarrays reveal hundreds of regulated genes in the dorsal root ganglion after peripheral nerve injury.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139981/
https://www.ncbi.nlm.nih.gov/pubmed/12401135
http://dx.doi.org/10.1186/1471-2202-3-16
work_keys_str_mv AT costiganmichael replicatehighdensityratgenomeoligonucleotidemicroarraysrevealhundredsofregulatedgenesinthedorsalrootganglionafterperipheralnerveinjury
AT befortkatia replicatehighdensityratgenomeoligonucleotidemicroarraysrevealhundredsofregulatedgenesinthedorsalrootganglionafterperipheralnerveinjury
AT karchewskilaurie replicatehighdensityratgenomeoligonucleotidemicroarraysrevealhundredsofregulatedgenesinthedorsalrootganglionafterperipheralnerveinjury
AT griffinroberts replicatehighdensityratgenomeoligonucleotidemicroarraysrevealhundredsofregulatedgenesinthedorsalrootganglionafterperipheralnerveinjury
AT dursodonatella replicatehighdensityratgenomeoligonucleotidemicroarraysrevealhundredsofregulatedgenesinthedorsalrootganglionafterperipheralnerveinjury
AT allchorneandrew replicatehighdensityratgenomeoligonucleotidemicroarraysrevealhundredsofregulatedgenesinthedorsalrootganglionafterperipheralnerveinjury
AT sitarskijoanne replicatehighdensityratgenomeoligonucleotidemicroarraysrevealhundredsofregulatedgenesinthedorsalrootganglionafterperipheralnerveinjury
AT mannionjamesw replicatehighdensityratgenomeoligonucleotidemicroarraysrevealhundredsofregulatedgenesinthedorsalrootganglionafterperipheralnerveinjury
AT prattricharde replicatehighdensityratgenomeoligonucleotidemicroarraysrevealhundredsofregulatedgenesinthedorsalrootganglionafterperipheralnerveinjury
AT woolfcliffordj replicatehighdensityratgenomeoligonucleotidemicroarraysrevealhundredsofregulatedgenesinthedorsalrootganglionafterperipheralnerveinjury