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Validation of commonly used reference genes for sleep-related gene expression studies

BACKGROUND: Sleep is a restorative process and is essential for maintenance of mental and physical health. In an attempt to understand the complexity of sleep, multidisciplinary strategies, including genetic approaches, have been applied to sleep research. Although quantitative real time PCR has bee...

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Autores principales: Lee, Kil S, Alvarenga, Tathiana A, Guindalini, Camila, Andersen, Monica L, Castro, Rosa MRPS, Tufik, Sergio
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2685383/
https://www.ncbi.nlm.nih.gov/pubmed/19445681
http://dx.doi.org/10.1186/1471-2199-10-45
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author Lee, Kil S
Alvarenga, Tathiana A
Guindalini, Camila
Andersen, Monica L
Castro, Rosa MRPS
Tufik, Sergio
author_facet Lee, Kil S
Alvarenga, Tathiana A
Guindalini, Camila
Andersen, Monica L
Castro, Rosa MRPS
Tufik, Sergio
author_sort Lee, Kil S
collection PubMed
description BACKGROUND: Sleep is a restorative process and is essential for maintenance of mental and physical health. In an attempt to understand the complexity of sleep, multidisciplinary strategies, including genetic approaches, have been applied to sleep research. Although quantitative real time PCR has been used in previous sleep-related gene expression studies, proper validation of reference genes is currently lacking. Thus, we examined the effect of total or paradoxical sleep deprivation (TSD or PSD) on the expression stability of the following frequently used reference genes in brain and blood: beta-actin (b-actin), beta-2-microglobulin (B2M), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and hypoxanthine guanine phosphoribosyl transferase (HPRT). RESULTS: Neither TSD nor PSD affected the expression stability of all tested genes in both tissues indicating that b-actin, B2M, GAPDH and HPRT are appropriate reference genes for the sleep-related gene expression studies. In order to further verify these results, the relative expression of brain derived neurotrophic factor (BDNF) and glycerol-3-phosphate dehydrogenase1 (GPD1) was evaluated in brain and blood, respectively. The normalization with each of four reference genes produced similar pattern of expression in control and sleep deprived rats, but subtle differences in the magnitude of expression fold change were observed which might affect the statistical significance. CONCLUSION: This study demonstrated that sleep deprivation does not alter the expression stability of commonly used reference genes in brain and blood. Nonetheless, the use of multiple reference genes in quantitative RT-PCR is required for the accurate results.
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spelling pubmed-26853832009-05-22 Validation of commonly used reference genes for sleep-related gene expression studies Lee, Kil S Alvarenga, Tathiana A Guindalini, Camila Andersen, Monica L Castro, Rosa MRPS Tufik, Sergio BMC Mol Biol Research Article BACKGROUND: Sleep is a restorative process and is essential for maintenance of mental and physical health. In an attempt to understand the complexity of sleep, multidisciplinary strategies, including genetic approaches, have been applied to sleep research. Although quantitative real time PCR has been used in previous sleep-related gene expression studies, proper validation of reference genes is currently lacking. Thus, we examined the effect of total or paradoxical sleep deprivation (TSD or PSD) on the expression stability of the following frequently used reference genes in brain and blood: beta-actin (b-actin), beta-2-microglobulin (B2M), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and hypoxanthine guanine phosphoribosyl transferase (HPRT). RESULTS: Neither TSD nor PSD affected the expression stability of all tested genes in both tissues indicating that b-actin, B2M, GAPDH and HPRT are appropriate reference genes for the sleep-related gene expression studies. In order to further verify these results, the relative expression of brain derived neurotrophic factor (BDNF) and glycerol-3-phosphate dehydrogenase1 (GPD1) was evaluated in brain and blood, respectively. The normalization with each of four reference genes produced similar pattern of expression in control and sleep deprived rats, but subtle differences in the magnitude of expression fold change were observed which might affect the statistical significance. CONCLUSION: This study demonstrated that sleep deprivation does not alter the expression stability of commonly used reference genes in brain and blood. Nonetheless, the use of multiple reference genes in quantitative RT-PCR is required for the accurate results. BioMed Central 2009-05-15 /pmc/articles/PMC2685383/ /pubmed/19445681 http://dx.doi.org/10.1186/1471-2199-10-45 Text en Copyright © 2009 Lee 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
Lee, Kil S
Alvarenga, Tathiana A
Guindalini, Camila
Andersen, Monica L
Castro, Rosa MRPS
Tufik, Sergio
Validation of commonly used reference genes for sleep-related gene expression studies
title Validation of commonly used reference genes for sleep-related gene expression studies
title_full Validation of commonly used reference genes for sleep-related gene expression studies
title_fullStr Validation of commonly used reference genes for sleep-related gene expression studies
title_full_unstemmed Validation of commonly used reference genes for sleep-related gene expression studies
title_short Validation of commonly used reference genes for sleep-related gene expression studies
title_sort validation of commonly used reference genes for sleep-related gene expression studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2685383/
https://www.ncbi.nlm.nih.gov/pubmed/19445681
http://dx.doi.org/10.1186/1471-2199-10-45
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