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Genome-wide profiling of G protein-coupled receptors in cerebellar granule neurons using high-throughput, real-time PCR
BACKGROUND: G protein-coupled receptors (GPCRs) are major players in cell communication, regulate a whole range of physiological functions during development and throughout adult life, are affected in numerous pathological situations, and constitute so far the largest class of drugable targets for h...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111393/ https://www.ncbi.nlm.nih.gov/pubmed/21575240 http://dx.doi.org/10.1186/1471-2164-12-241 |
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author | Maurel, Benjamin Le Digarcher, Anne Dantec, Christelle Journot, Laurent |
author_facet | Maurel, Benjamin Le Digarcher, Anne Dantec, Christelle Journot, Laurent |
author_sort | Maurel, Benjamin |
collection | PubMed |
description | BACKGROUND: G protein-coupled receptors (GPCRs) are major players in cell communication, regulate a whole range of physiological functions during development and throughout adult life, are affected in numerous pathological situations, and constitute so far the largest class of drugable targets for human diseases. The corresponding genes are usually expressed at low levels, making accurate, genome-wide quantification of their expression levels a challenging task using microarrays. RESULTS: We first draw an inventory of all endo-GPCRs encoded in the murine genome. To profile GPCRs genome-wide accurately, sensitively, comprehensively, and cost-effectively, we designed and validated a collection of primers that we used in quantitative RT-PCR experiments. We experimentally validated a statistical approach to analyze genome-wide, real-time PCR data. To illustrate the usefulness of this approach, we determined the repertoire of GPCRs expressed in cerebellar granule neurons and neuroblasts during postnatal development. CONCLUSIONS: We identified tens of GPCRs that were not detected previously in this cell type; these GPCRs represent novel candidate players in the development and survival of cerebellar granule neurons. The sequences of primers used in this study are freely available to those interested in quantifying GPCR expression comprehensively. |
format | Online Article Text |
id | pubmed-3111393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31113932011-06-10 Genome-wide profiling of G protein-coupled receptors in cerebellar granule neurons using high-throughput, real-time PCR Maurel, Benjamin Le Digarcher, Anne Dantec, Christelle Journot, Laurent BMC Genomics Methodology Article BACKGROUND: G protein-coupled receptors (GPCRs) are major players in cell communication, regulate a whole range of physiological functions during development and throughout adult life, are affected in numerous pathological situations, and constitute so far the largest class of drugable targets for human diseases. The corresponding genes are usually expressed at low levels, making accurate, genome-wide quantification of their expression levels a challenging task using microarrays. RESULTS: We first draw an inventory of all endo-GPCRs encoded in the murine genome. To profile GPCRs genome-wide accurately, sensitively, comprehensively, and cost-effectively, we designed and validated a collection of primers that we used in quantitative RT-PCR experiments. We experimentally validated a statistical approach to analyze genome-wide, real-time PCR data. To illustrate the usefulness of this approach, we determined the repertoire of GPCRs expressed in cerebellar granule neurons and neuroblasts during postnatal development. CONCLUSIONS: We identified tens of GPCRs that were not detected previously in this cell type; these GPCRs represent novel candidate players in the development and survival of cerebellar granule neurons. The sequences of primers used in this study are freely available to those interested in quantifying GPCR expression comprehensively. BioMed Central 2011-05-16 /pmc/articles/PMC3111393/ /pubmed/21575240 http://dx.doi.org/10.1186/1471-2164-12-241 Text en Copyright ©2011 Maurel 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 Article Maurel, Benjamin Le Digarcher, Anne Dantec, Christelle Journot, Laurent Genome-wide profiling of G protein-coupled receptors in cerebellar granule neurons using high-throughput, real-time PCR |
title | Genome-wide profiling of G protein-coupled receptors in cerebellar granule neurons using high-throughput, real-time PCR |
title_full | Genome-wide profiling of G protein-coupled receptors in cerebellar granule neurons using high-throughput, real-time PCR |
title_fullStr | Genome-wide profiling of G protein-coupled receptors in cerebellar granule neurons using high-throughput, real-time PCR |
title_full_unstemmed | Genome-wide profiling of G protein-coupled receptors in cerebellar granule neurons using high-throughput, real-time PCR |
title_short | Genome-wide profiling of G protein-coupled receptors in cerebellar granule neurons using high-throughput, real-time PCR |
title_sort | genome-wide profiling of g protein-coupled receptors in cerebellar granule neurons using high-throughput, real-time pcr |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111393/ https://www.ncbi.nlm.nih.gov/pubmed/21575240 http://dx.doi.org/10.1186/1471-2164-12-241 |
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