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Housekeeping genes for quantitative expression studies in the three-spined stickleback Gasterosteus aculeatus
BACKGROUND: During the last years the quantification of immune response under immunological challenges, e.g. parasitation, has been a major focus of research. In this context, the expression of immune response genes in teleost fish has been surveyed for scientific and commercial purposes. Despite th...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2254436/ https://www.ncbi.nlm.nih.gov/pubmed/18230138 http://dx.doi.org/10.1186/1471-2199-9-18 |
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author | Hibbeler, Sascha Scharsack, Joern P Becker, Sven |
author_facet | Hibbeler, Sascha Scharsack, Joern P Becker, Sven |
author_sort | Hibbeler, Sascha |
collection | PubMed |
description | BACKGROUND: During the last years the quantification of immune response under immunological challenges, e.g. parasitation, has been a major focus of research. In this context, the expression of immune response genes in teleost fish has been surveyed for scientific and commercial purposes. Despite the fact that it was shown in teleostei and other taxa that the gene for beta-actin is not the most stably expressed housekeeping gene (HKG), depending on the tissue and experimental treatment, the gene has been used as a reference gene in such studies. In the three-spined stickleback, Gasterosteus aculeatus, other HKG than the one for beta-actin have not been established so far. RESULTS: To establish a reliable method for the measurement of immune gene expression in Gasterosteus aculeatus, sequences from the now available genome database and an EST library of the same species were used to select oligonucleotide primers for HKG, in order to perform quantitative reverse-transcription (RT) PCR. The expression stability of ten candidate reference genes was evaluated in three different tissues, and in five parasite treatment groups, using the three algorithms BestKeeper, geNorm and NormFinder. Our results showed that in most of the tissues and treatments HKG that could not be used so far due to unknown sequences, proved to be more stably expressed than the one for beta-actin. CONCLUSION: As they were the most stably expressed genes in all tissues examined, we suggest using the genes for the L13a ribosomal binding protein and ubiquitin as alternative or additional reference genes in expression analysis in Gasterosteus aculeatus. |
format | Text |
id | pubmed-2254436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22544362008-02-26 Housekeeping genes for quantitative expression studies in the three-spined stickleback Gasterosteus aculeatus Hibbeler, Sascha Scharsack, Joern P Becker, Sven BMC Mol Biol Research Article BACKGROUND: During the last years the quantification of immune response under immunological challenges, e.g. parasitation, has been a major focus of research. In this context, the expression of immune response genes in teleost fish has been surveyed for scientific and commercial purposes. Despite the fact that it was shown in teleostei and other taxa that the gene for beta-actin is not the most stably expressed housekeeping gene (HKG), depending on the tissue and experimental treatment, the gene has been used as a reference gene in such studies. In the three-spined stickleback, Gasterosteus aculeatus, other HKG than the one for beta-actin have not been established so far. RESULTS: To establish a reliable method for the measurement of immune gene expression in Gasterosteus aculeatus, sequences from the now available genome database and an EST library of the same species were used to select oligonucleotide primers for HKG, in order to perform quantitative reverse-transcription (RT) PCR. The expression stability of ten candidate reference genes was evaluated in three different tissues, and in five parasite treatment groups, using the three algorithms BestKeeper, geNorm and NormFinder. Our results showed that in most of the tissues and treatments HKG that could not be used so far due to unknown sequences, proved to be more stably expressed than the one for beta-actin. CONCLUSION: As they were the most stably expressed genes in all tissues examined, we suggest using the genes for the L13a ribosomal binding protein and ubiquitin as alternative or additional reference genes in expression analysis in Gasterosteus aculeatus. BioMed Central 2008-01-29 /pmc/articles/PMC2254436/ /pubmed/18230138 http://dx.doi.org/10.1186/1471-2199-9-18 Text en Copyright © 2008 Hibbeler 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 Hibbeler, Sascha Scharsack, Joern P Becker, Sven Housekeeping genes for quantitative expression studies in the three-spined stickleback Gasterosteus aculeatus |
title | Housekeeping genes for quantitative expression studies in the three-spined stickleback Gasterosteus aculeatus |
title_full | Housekeeping genes for quantitative expression studies in the three-spined stickleback Gasterosteus aculeatus |
title_fullStr | Housekeeping genes for quantitative expression studies in the three-spined stickleback Gasterosteus aculeatus |
title_full_unstemmed | Housekeeping genes for quantitative expression studies in the three-spined stickleback Gasterosteus aculeatus |
title_short | Housekeeping genes for quantitative expression studies in the three-spined stickleback Gasterosteus aculeatus |
title_sort | housekeeping genes for quantitative expression studies in the three-spined stickleback gasterosteus aculeatus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2254436/ https://www.ncbi.nlm.nih.gov/pubmed/18230138 http://dx.doi.org/10.1186/1471-2199-9-18 |
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