Cargando…

Quantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo and in vitro

BACKGROUND: Real-time PCR is an efficient tool to measure transcripts and provide valuable quantitative information on gene expression of preimplantation stage embryos. Finding valid reference genes for normalization is essential to interpret the real-time PCR results accurately, and understand the...

Descripción completa

Detalles Bibliográficos
Autores principales: Mamo, Solomon, Gal, Arpad Baji, Bodo, Szilard, Dinnyes, Andras
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1832186/
https://www.ncbi.nlm.nih.gov/pubmed/17341302
http://dx.doi.org/10.1186/1471-213X-7-14
_version_ 1782132812233572352
author Mamo, Solomon
Gal, Arpad Baji
Bodo, Szilard
Dinnyes, Andras
author_facet Mamo, Solomon
Gal, Arpad Baji
Bodo, Szilard
Dinnyes, Andras
author_sort Mamo, Solomon
collection PubMed
description BACKGROUND: Real-time PCR is an efficient tool to measure transcripts and provide valuable quantitative information on gene expression of preimplantation stage embryos. Finding valid reference genes for normalization is essential to interpret the real-time PCR results accurately, and understand the biological dynamics during early development. The use of reference genes also known as housekeeping genes is the most widely applied approach. However, the different genes are not systematically compared, and as a result there is no uniformity between studies in selecting the reference gene. The goals of this study were to compare a wide selection of the most commonly used housekeeping genes in mouse oocytes and preimplantation stage embryos produced under different culture conditions, and select the best stable genes for normalization of gene expression data. RESULTS: Quantitative real time PCR method was used to evaluate 12 commonly used housekeeping genes (Actb, Gapdh, H2afz, Hprt, Ppia, Ubc, Eef1e1, Tubb4, Hist2h2aa1, Tbp, Bmp7, Polr2a) in multiple individual embryos representing six different developmental stages. The results were analysed, and stable genes were selected using the geNorm software. The expression pattern was almost similar despite differences in the culture system; however, the transcript levels were affected by culture conditions. The genes have showed various stabilities, and have been ranked accordingly. CONCLUSION: Compared to earlier studies with similar objectives, we used a unique approach in analysing larger number of genes, comparing embryo samples derived in vivo or in vitro, analysing the expression in the early and late maternal to zygote transition periods separately, and using multiple individual embryos. Based on detailed quantification, pattern analyses and using the geNorm application, we found Ppia, H2afz and Hprt1 genes to be the most stable across the different stages and culture conditions, while Actb, the classical housekeeping gene, showed the least stability. We recommend the use of the geometric averages of those three genes for normalization in mouse preimplantation-stage gene expression studies.
format Text
id pubmed-1832186
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-18321862007-03-27 Quantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo and in vitro Mamo, Solomon Gal, Arpad Baji Bodo, Szilard Dinnyes, Andras BMC Dev Biol Research Article BACKGROUND: Real-time PCR is an efficient tool to measure transcripts and provide valuable quantitative information on gene expression of preimplantation stage embryos. Finding valid reference genes for normalization is essential to interpret the real-time PCR results accurately, and understand the biological dynamics during early development. The use of reference genes also known as housekeeping genes is the most widely applied approach. However, the different genes are not systematically compared, and as a result there is no uniformity between studies in selecting the reference gene. The goals of this study were to compare a wide selection of the most commonly used housekeeping genes in mouse oocytes and preimplantation stage embryos produced under different culture conditions, and select the best stable genes for normalization of gene expression data. RESULTS: Quantitative real time PCR method was used to evaluate 12 commonly used housekeeping genes (Actb, Gapdh, H2afz, Hprt, Ppia, Ubc, Eef1e1, Tubb4, Hist2h2aa1, Tbp, Bmp7, Polr2a) in multiple individual embryos representing six different developmental stages. The results were analysed, and stable genes were selected using the geNorm software. The expression pattern was almost similar despite differences in the culture system; however, the transcript levels were affected by culture conditions. The genes have showed various stabilities, and have been ranked accordingly. CONCLUSION: Compared to earlier studies with similar objectives, we used a unique approach in analysing larger number of genes, comparing embryo samples derived in vivo or in vitro, analysing the expression in the early and late maternal to zygote transition periods separately, and using multiple individual embryos. Based on detailed quantification, pattern analyses and using the geNorm application, we found Ppia, H2afz and Hprt1 genes to be the most stable across the different stages and culture conditions, while Actb, the classical housekeeping gene, showed the least stability. We recommend the use of the geometric averages of those three genes for normalization in mouse preimplantation-stage gene expression studies. BioMed Central 2007-03-06 /pmc/articles/PMC1832186/ /pubmed/17341302 http://dx.doi.org/10.1186/1471-213X-7-14 Text en Copyright © 2007 Mamo 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
Mamo, Solomon
Gal, Arpad Baji
Bodo, Szilard
Dinnyes, Andras
Quantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo and in vitro
title Quantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo and in vitro
title_full Quantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo and in vitro
title_fullStr Quantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo and in vitro
title_full_unstemmed Quantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo and in vitro
title_short Quantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo and in vitro
title_sort quantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo and in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1832186/
https://www.ncbi.nlm.nih.gov/pubmed/17341302
http://dx.doi.org/10.1186/1471-213X-7-14
work_keys_str_mv AT mamosolomon quantitativeevaluationandselectionofreferencegenesinmouseoocytesandembryosculturedinvivoandinvitro
AT galarpadbaji quantitativeevaluationandselectionofreferencegenesinmouseoocytesandembryosculturedinvivoandinvitro
AT bodoszilard quantitativeevaluationandselectionofreferencegenesinmouseoocytesandembryosculturedinvivoandinvitro
AT dinnyesandras quantitativeevaluationandselectionofreferencegenesinmouseoocytesandembryosculturedinvivoandinvitro