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Transcriptome profiling of bovine inner cell mass and trophectoderm derived from in vivo generated blastocysts
BACKGROUND: This study describes the generation and analysis of the transcriptional profile of bovine inner cell mass (ICM) and trophectoderm (TE), obtained from in vivo developed embryos by using a bovine-embryo specific array (EmbryoGENE) containing 37,238 probes. RESULTS: A total of 4,689 probes...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683974/ https://www.ncbi.nlm.nih.gov/pubmed/26681441 http://dx.doi.org/10.1186/s12861-015-0096-3 |
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author | Hosseini, S. M. Dufort, I. Caballero, J. Moulavi, F. Ghanaei, H. R. Sirard, M. A. |
author_facet | Hosseini, S. M. Dufort, I. Caballero, J. Moulavi, F. Ghanaei, H. R. Sirard, M. A. |
author_sort | Hosseini, S. M. |
collection | PubMed |
description | BACKGROUND: This study describes the generation and analysis of the transcriptional profile of bovine inner cell mass (ICM) and trophectoderm (TE), obtained from in vivo developed embryos by using a bovine-embryo specific array (EmbryoGENE) containing 37,238 probes. RESULTS: A total of 4,689 probes were differentially expressed between ICM and TE, among these, 2,380 and 2,309 probes were upregulated in ICM and TE tissues, respectively (P ≤ 0.01, FC ≥ 2.0, FDR: 2.0). Ontological classification of the genes predominantly expressed in ICM emerged a range of functional categories with a preponderance of genes involved in basal and developmental signaling pathways including P53, TGFβ, IL8, mTOR, integrin, ILK, and ELF2 signalings. Cross-referencing of microarray data with two available in vitro studies indicated a marked reduction in ICM vs. TE transcriptional difference following in vitro culture of bovine embryos. Moreover, a great majority of genes that were found to be misregulated following in vitro culture of bovine embryos were known genes involved in epigenetic regulation of pluripotency and cell differentiation including DNMT1, GADD45, CARM1, ELF5 HDAC8, CCNB1, KDM6A, PRDM9, CDX2, ARID3A, IL6, GADD45A, FGFR2, PPP2R2B, and SMARCA2. Cross-species referencing of microarray data revealed substantial divergence between bovine and mouse and human in signaling pathways involved in early lineage specification. CONCLUSIONS: The transcriptional changes occur during ICM and TE lineages specification in bovine is greater than previously understood. Therefore, this array data establishes a standard to evaluate the in vitro imprint on the transcriptome and to hypothesize the cross-species differences that allow in vitro acquisition of pluripotent ICM in human and mice but hinder that process in bovine. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12861-015-0096-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4683974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46839742015-12-19 Transcriptome profiling of bovine inner cell mass and trophectoderm derived from in vivo generated blastocysts Hosseini, S. M. Dufort, I. Caballero, J. Moulavi, F. Ghanaei, H. R. Sirard, M. A. BMC Dev Biol Research Article BACKGROUND: This study describes the generation and analysis of the transcriptional profile of bovine inner cell mass (ICM) and trophectoderm (TE), obtained from in vivo developed embryos by using a bovine-embryo specific array (EmbryoGENE) containing 37,238 probes. RESULTS: A total of 4,689 probes were differentially expressed between ICM and TE, among these, 2,380 and 2,309 probes were upregulated in ICM and TE tissues, respectively (P ≤ 0.01, FC ≥ 2.0, FDR: 2.0). Ontological classification of the genes predominantly expressed in ICM emerged a range of functional categories with a preponderance of genes involved in basal and developmental signaling pathways including P53, TGFβ, IL8, mTOR, integrin, ILK, and ELF2 signalings. Cross-referencing of microarray data with two available in vitro studies indicated a marked reduction in ICM vs. TE transcriptional difference following in vitro culture of bovine embryos. Moreover, a great majority of genes that were found to be misregulated following in vitro culture of bovine embryos were known genes involved in epigenetic regulation of pluripotency and cell differentiation including DNMT1, GADD45, CARM1, ELF5 HDAC8, CCNB1, KDM6A, PRDM9, CDX2, ARID3A, IL6, GADD45A, FGFR2, PPP2R2B, and SMARCA2. Cross-species referencing of microarray data revealed substantial divergence between bovine and mouse and human in signaling pathways involved in early lineage specification. CONCLUSIONS: The transcriptional changes occur during ICM and TE lineages specification in bovine is greater than previously understood. Therefore, this array data establishes a standard to evaluate the in vitro imprint on the transcriptome and to hypothesize the cross-species differences that allow in vitro acquisition of pluripotent ICM in human and mice but hinder that process in bovine. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12861-015-0096-3) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-18 /pmc/articles/PMC4683974/ /pubmed/26681441 http://dx.doi.org/10.1186/s12861-015-0096-3 Text en © Hosseini et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Hosseini, S. M. Dufort, I. Caballero, J. Moulavi, F. Ghanaei, H. R. Sirard, M. A. Transcriptome profiling of bovine inner cell mass and trophectoderm derived from in vivo generated blastocysts |
title | Transcriptome profiling of bovine inner cell mass and trophectoderm derived from in vivo generated blastocysts |
title_full | Transcriptome profiling of bovine inner cell mass and trophectoderm derived from in vivo generated blastocysts |
title_fullStr | Transcriptome profiling of bovine inner cell mass and trophectoderm derived from in vivo generated blastocysts |
title_full_unstemmed | Transcriptome profiling of bovine inner cell mass and trophectoderm derived from in vivo generated blastocysts |
title_short | Transcriptome profiling of bovine inner cell mass and trophectoderm derived from in vivo generated blastocysts |
title_sort | transcriptome profiling of bovine inner cell mass and trophectoderm derived from in vivo generated blastocysts |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4683974/ https://www.ncbi.nlm.nih.gov/pubmed/26681441 http://dx.doi.org/10.1186/s12861-015-0096-3 |
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