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Identification and validation of suitable endogenous reference genes for gene expression studies in human peripheral blood

BACKGROUND: Gene expression studies require appropriate normalization methods. One such method uses stably expressed reference genes. Since suitable reference genes appear to be unique for each tissue, we have identified an optimal set of the most stably expressed genes in human blood that can be us...

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Autores principales: Stamova, Boryana S, Apperson, Michelle, Walker, Wynn L, Tian, Yingfang, Xu, Huichun, Adamczy, Peter, Zhan, Xinhua, Liu, Da-Zhi, Ander, Bradley P, Liao, Isaac H, Gregg, Jeffrey P, Turner, Renee J, Jickling, Glen, Lit, Lisa, Sharp, Frank R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2736983/
https://www.ncbi.nlm.nih.gov/pubmed/19656400
http://dx.doi.org/10.1186/1755-8794-2-49
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author Stamova, Boryana S
Apperson, Michelle
Walker, Wynn L
Tian, Yingfang
Xu, Huichun
Adamczy, Peter
Zhan, Xinhua
Liu, Da-Zhi
Ander, Bradley P
Liao, Isaac H
Gregg, Jeffrey P
Turner, Renee J
Jickling, Glen
Lit, Lisa
Sharp, Frank R
author_facet Stamova, Boryana S
Apperson, Michelle
Walker, Wynn L
Tian, Yingfang
Xu, Huichun
Adamczy, Peter
Zhan, Xinhua
Liu, Da-Zhi
Ander, Bradley P
Liao, Isaac H
Gregg, Jeffrey P
Turner, Renee J
Jickling, Glen
Lit, Lisa
Sharp, Frank R
author_sort Stamova, Boryana S
collection PubMed
description BACKGROUND: Gene expression studies require appropriate normalization methods. One such method uses stably expressed reference genes. Since suitable reference genes appear to be unique for each tissue, we have identified an optimal set of the most stably expressed genes in human blood that can be used for normalization. METHODS: Whole-genome Affymetrix Human 2.0 Plus arrays were examined from 526 samples of males and females ages 2 to 78, including control subjects and patients with Tourette syndrome, stroke, migraine, muscular dystrophy, and autism. The top 100 most stably expressed genes with a broad range of expression levels were identified. To validate the best candidate genes, we performed quantitative RT-PCR on a subset of 10 genes (TRAP1, DECR1, FPGS, FARP1, MAPRE2, PEX16, GINS2, CRY2, CSNK1G2 and A4GALT), 4 commonly employed reference genes (GAPDH, ACTB, B2M and HMBS) and PPIB, previously reported to be stably expressed in blood. Expression stability and ranking analysis were performed using GeNorm and NormFinder algorithms. RESULTS: Reference genes were ranked based on their expression stability and the minimum number of genes needed for nomalization as calculated using GeNorm showed that the fewest, most stably expressed genes needed for acurate normalization in RNA expression studies of human whole blood is a combination of TRAP1, FPGS, DECR1 and PPIB. We confirmed the ranking of the best candidate control genes by using an alternative algorithm (NormFinder). CONCLUSION: The reference genes identified in this study are stably expressed in whole blood of humans of both genders with multiple disease conditions and ages 2 to 78. Importantly, they also have different functions within cells and thus should be expressed independently of each other. These genes should be useful as normalization genes for microarray and RT-PCR whole blood studies of human physiology, metabolism and disease.
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spelling pubmed-27369832009-09-03 Identification and validation of suitable endogenous reference genes for gene expression studies in human peripheral blood Stamova, Boryana S Apperson, Michelle Walker, Wynn L Tian, Yingfang Xu, Huichun Adamczy, Peter Zhan, Xinhua Liu, Da-Zhi Ander, Bradley P Liao, Isaac H Gregg, Jeffrey P Turner, Renee J Jickling, Glen Lit, Lisa Sharp, Frank R BMC Med Genomics Research Article BACKGROUND: Gene expression studies require appropriate normalization methods. One such method uses stably expressed reference genes. Since suitable reference genes appear to be unique for each tissue, we have identified an optimal set of the most stably expressed genes in human blood that can be used for normalization. METHODS: Whole-genome Affymetrix Human 2.0 Plus arrays were examined from 526 samples of males and females ages 2 to 78, including control subjects and patients with Tourette syndrome, stroke, migraine, muscular dystrophy, and autism. The top 100 most stably expressed genes with a broad range of expression levels were identified. To validate the best candidate genes, we performed quantitative RT-PCR on a subset of 10 genes (TRAP1, DECR1, FPGS, FARP1, MAPRE2, PEX16, GINS2, CRY2, CSNK1G2 and A4GALT), 4 commonly employed reference genes (GAPDH, ACTB, B2M and HMBS) and PPIB, previously reported to be stably expressed in blood. Expression stability and ranking analysis were performed using GeNorm and NormFinder algorithms. RESULTS: Reference genes were ranked based on their expression stability and the minimum number of genes needed for nomalization as calculated using GeNorm showed that the fewest, most stably expressed genes needed for acurate normalization in RNA expression studies of human whole blood is a combination of TRAP1, FPGS, DECR1 and PPIB. We confirmed the ranking of the best candidate control genes by using an alternative algorithm (NormFinder). CONCLUSION: The reference genes identified in this study are stably expressed in whole blood of humans of both genders with multiple disease conditions and ages 2 to 78. Importantly, they also have different functions within cells and thus should be expressed independently of each other. These genes should be useful as normalization genes for microarray and RT-PCR whole blood studies of human physiology, metabolism and disease. BioMed Central 2009-08-05 /pmc/articles/PMC2736983/ /pubmed/19656400 http://dx.doi.org/10.1186/1755-8794-2-49 Text en Copyright © 2009 Stamova 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 Research Article
Stamova, Boryana S
Apperson, Michelle
Walker, Wynn L
Tian, Yingfang
Xu, Huichun
Adamczy, Peter
Zhan, Xinhua
Liu, Da-Zhi
Ander, Bradley P
Liao, Isaac H
Gregg, Jeffrey P
Turner, Renee J
Jickling, Glen
Lit, Lisa
Sharp, Frank R
Identification and validation of suitable endogenous reference genes for gene expression studies in human peripheral blood
title Identification and validation of suitable endogenous reference genes for gene expression studies in human peripheral blood
title_full Identification and validation of suitable endogenous reference genes for gene expression studies in human peripheral blood
title_fullStr Identification and validation of suitable endogenous reference genes for gene expression studies in human peripheral blood
title_full_unstemmed Identification and validation of suitable endogenous reference genes for gene expression studies in human peripheral blood
title_short Identification and validation of suitable endogenous reference genes for gene expression studies in human peripheral blood
title_sort identification and validation of suitable endogenous reference genes for gene expression studies in human peripheral blood
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2736983/
https://www.ncbi.nlm.nih.gov/pubmed/19656400
http://dx.doi.org/10.1186/1755-8794-2-49
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