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Expression of genes associated with BMP signaling pathway in porcine oocytes before and after IVM – a microarray approach

BACKGROUND: The full maturational capability of mammalian oocytes is accompanied by nuclear and cytoplasmic modifications, which are associated with proliferation and differentiation of surrounding cumulus cells. These events are regulated on molecular level by the expression of target genes involve...

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Autores principales: Budna, Joanna, Rybska, Marta, Ciesiółka, Sylwia, Bryja, Artur, Borys, Sylwia, Kranc, Wiesława, Wojtanowicz-Markiewicz, Katarzyna, Jeseta, Michal, Sumelka, Ewa, Bukowska, Dorota, Antosik, Paweł, Brüssow, Klaus P., Bruska, Małgorzata, Nowicki, Michał, Zabel, Maciej, Kempisty, Bartosz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457624/
https://www.ncbi.nlm.nih.gov/pubmed/28576120
http://dx.doi.org/10.1186/s12958-017-0261-6
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author Budna, Joanna
Rybska, Marta
Ciesiółka, Sylwia
Bryja, Artur
Borys, Sylwia
Kranc, Wiesława
Wojtanowicz-Markiewicz, Katarzyna
Jeseta, Michal
Sumelka, Ewa
Bukowska, Dorota
Antosik, Paweł
Brüssow, Klaus P.
Bruska, Małgorzata
Nowicki, Michał
Zabel, Maciej
Kempisty, Bartosz
author_facet Budna, Joanna
Rybska, Marta
Ciesiółka, Sylwia
Bryja, Artur
Borys, Sylwia
Kranc, Wiesława
Wojtanowicz-Markiewicz, Katarzyna
Jeseta, Michal
Sumelka, Ewa
Bukowska, Dorota
Antosik, Paweł
Brüssow, Klaus P.
Bruska, Małgorzata
Nowicki, Michał
Zabel, Maciej
Kempisty, Bartosz
author_sort Budna, Joanna
collection PubMed
description BACKGROUND: The full maturational capability of mammalian oocytes is accompanied by nuclear and cytoplasmic modifications, which are associated with proliferation and differentiation of surrounding cumulus cells. These events are regulated on molecular level by the expression of target genes involved in signal transduction pathways crucial for folliculogenesis and oogenesis. Transforming growth factor beta signaling includes several molecules that are involved in the regulation of oogenesis and embryo growth, including bone morphogenetic protein (BMP). However, the BMP-related gene expression profile in oocytes at different maturational stages requires further investigation. METHODS: Oocytes were isolated from pubertal crossbred Landrace gilts follicles, selected with a use of BCB staining test and analyzed before and after in vitro maturation. Gene expression profiles were examined using an Affymetrix microarray approach and validated by RT-qPCR. Database for Annotation, Visualization, and Integrated Discovery (DAVID) software was used for the extraction of the genes belonging to a BMP-signaling pathway ontology group. RESULTS: The assay revealed 12,258 different transcripts in porcine oocytes, among which 379 genes were down-regulated and 40 were up-regulated. The DAVID database indicated a “BMP signaling pathway” ontology group, which was significantly regulated in both groups of oocytes. We discovered five up-regulated genes in oocytes before versus after in vitro maturation (IVM): chordin-like 1 (CHRDL1), follistatin (FST), transforming growth factor-beta receptor-type III (TGFβR3), decapentaplegic homolog 4 (SMAD4), and inhibitor of DNA binding 1 (ID1). CONCLUSIONS: Increased expression of CHRDL1, FST, TGFβR3, SMAD4, and ID1 transcripts before IVM suggested a subordinate role of the BMP signaling pathway in porcine oocyte maturational competence. Conversely, it is postulated that these genes are involved in early stages of folliculogenesis and oogenesis regulation in pigs, since in oocytes before IVM increased expression was observed.
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spelling pubmed-54576242017-06-06 Expression of genes associated with BMP signaling pathway in porcine oocytes before and after IVM – a microarray approach Budna, Joanna Rybska, Marta Ciesiółka, Sylwia Bryja, Artur Borys, Sylwia Kranc, Wiesława Wojtanowicz-Markiewicz, Katarzyna Jeseta, Michal Sumelka, Ewa Bukowska, Dorota Antosik, Paweł Brüssow, Klaus P. Bruska, Małgorzata Nowicki, Michał Zabel, Maciej Kempisty, Bartosz Reprod Biol Endocrinol Research BACKGROUND: The full maturational capability of mammalian oocytes is accompanied by nuclear and cytoplasmic modifications, which are associated with proliferation and differentiation of surrounding cumulus cells. These events are regulated on molecular level by the expression of target genes involved in signal transduction pathways crucial for folliculogenesis and oogenesis. Transforming growth factor beta signaling includes several molecules that are involved in the regulation of oogenesis and embryo growth, including bone morphogenetic protein (BMP). However, the BMP-related gene expression profile in oocytes at different maturational stages requires further investigation. METHODS: Oocytes were isolated from pubertal crossbred Landrace gilts follicles, selected with a use of BCB staining test and analyzed before and after in vitro maturation. Gene expression profiles were examined using an Affymetrix microarray approach and validated by RT-qPCR. Database for Annotation, Visualization, and Integrated Discovery (DAVID) software was used for the extraction of the genes belonging to a BMP-signaling pathway ontology group. RESULTS: The assay revealed 12,258 different transcripts in porcine oocytes, among which 379 genes were down-regulated and 40 were up-regulated. The DAVID database indicated a “BMP signaling pathway” ontology group, which was significantly regulated in both groups of oocytes. We discovered five up-regulated genes in oocytes before versus after in vitro maturation (IVM): chordin-like 1 (CHRDL1), follistatin (FST), transforming growth factor-beta receptor-type III (TGFβR3), decapentaplegic homolog 4 (SMAD4), and inhibitor of DNA binding 1 (ID1). CONCLUSIONS: Increased expression of CHRDL1, FST, TGFβR3, SMAD4, and ID1 transcripts before IVM suggested a subordinate role of the BMP signaling pathway in porcine oocyte maturational competence. Conversely, it is postulated that these genes are involved in early stages of folliculogenesis and oogenesis regulation in pigs, since in oocytes before IVM increased expression was observed. BioMed Central 2017-06-02 /pmc/articles/PMC5457624/ /pubmed/28576120 http://dx.doi.org/10.1186/s12958-017-0261-6 Text en © The Author(s). 2017 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
Budna, Joanna
Rybska, Marta
Ciesiółka, Sylwia
Bryja, Artur
Borys, Sylwia
Kranc, Wiesława
Wojtanowicz-Markiewicz, Katarzyna
Jeseta, Michal
Sumelka, Ewa
Bukowska, Dorota
Antosik, Paweł
Brüssow, Klaus P.
Bruska, Małgorzata
Nowicki, Michał
Zabel, Maciej
Kempisty, Bartosz
Expression of genes associated with BMP signaling pathway in porcine oocytes before and after IVM – a microarray approach
title Expression of genes associated with BMP signaling pathway in porcine oocytes before and after IVM – a microarray approach
title_full Expression of genes associated with BMP signaling pathway in porcine oocytes before and after IVM – a microarray approach
title_fullStr Expression of genes associated with BMP signaling pathway in porcine oocytes before and after IVM – a microarray approach
title_full_unstemmed Expression of genes associated with BMP signaling pathway in porcine oocytes before and after IVM – a microarray approach
title_short Expression of genes associated with BMP signaling pathway in porcine oocytes before and after IVM – a microarray approach
title_sort expression of genes associated with bmp signaling pathway in porcine oocytes before and after ivm – a microarray approach
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457624/
https://www.ncbi.nlm.nih.gov/pubmed/28576120
http://dx.doi.org/10.1186/s12958-017-0261-6
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