Differential expression of genes in follicular cells of swines

The main purpose of the present study was to identify for candidate genes related to ovulation in swines. To do so, it was investigated in ovarian follicular cells through quantitative real-time PCR the differential expression of the following genes: steroidogenic acute regulator (STAR), GATA-binding protein 4 (GATA), prostaglandin F2α (PGF2α), progesterone receptor (P4R), follicle-stimulating hormone receptor (FSHR), and cytochrome P450 aromatase (CYP19). These genes encode hormone receptors (FSHR and P4R), hormone (PGF2α), steroidogenic proteins (STAR and CYP19) and transcription factor (GATA). Folicular cells were collected from sows with high and low number of piglets/litters during the follicular phase of the estrus cycle. There was difference in transcript abundance among low and high prolific sows for the STAR, GATA, PGF2α, P4R and CYP19 genes. For the FSHR gene, the fold change was not considered to be significantly different. Because in the present study only the transcript level of the above mentioned genes was analyzed, no inference can be made regarded to protein translation or activity. Therefore, gene sequence trials and other functional studies will be necessary to complement the present results, allowing a better understanding on biological complexity of these genes and their use as markers for prolificity in swines.

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Main Authors: Miranda-Furtado,Cristiana Libardi, Silva,Priscila Vendramini, Guimarães,Marta Fonseca Martins, Serão,Nicola Vergara Lopes, Guimarães,José Domingos, Guimarães,Simone Eliza Facioni
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Zootecnia 2010
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-35982010000500012
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spelling oai:scielo:S1516-359820100005000122010-08-31Differential expression of genes in follicular cells of swinesMiranda-Furtado,Cristiana LibardiSilva,Priscila VendraminiGuimarães,Marta Fonseca MartinsSerão,Nicola Vergara LopesGuimarães,José DomingosGuimarães,Simone Eliza Facioni candidate gene litter size ovulation rate pig production quantitative real-time PCR The main purpose of the present study was to identify for candidate genes related to ovulation in swines. To do so, it was investigated in ovarian follicular cells through quantitative real-time PCR the differential expression of the following genes: steroidogenic acute regulator (STAR), GATA-binding protein 4 (GATA), prostaglandin F2α (PGF2α), progesterone receptor (P4R), follicle-stimulating hormone receptor (FSHR), and cytochrome P450 aromatase (CYP19). These genes encode hormone receptors (FSHR and P4R), hormone (PGF2α), steroidogenic proteins (STAR and CYP19) and transcription factor (GATA). Folicular cells were collected from sows with high and low number of piglets/litters during the follicular phase of the estrus cycle. There was difference in transcript abundance among low and high prolific sows for the STAR, GATA, PGF2α, P4R and CYP19 genes. For the FSHR gene, the fold change was not considered to be significantly different. Because in the present study only the transcript level of the above mentioned genes was analyzed, no inference can be made regarded to protein translation or activity. Therefore, gene sequence trials and other functional studies will be necessary to complement the present results, allowing a better understanding on biological complexity of these genes and their use as markers for prolificity in swines.info:eu-repo/semantics/openAccessSociedade Brasileira de ZootecniaRevista Brasileira de Zootecnia v.39 n.5 20102010-05-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-35982010000500012en10.1590/S1516-35982010000500012
institution SCIELO
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country Brasil
countrycode BR
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libraryname SciELO
language English
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author Miranda-Furtado,Cristiana Libardi
Silva,Priscila Vendramini
Guimarães,Marta Fonseca Martins
Serão,Nicola Vergara Lopes
Guimarães,José Domingos
Guimarães,Simone Eliza Facioni
spellingShingle Miranda-Furtado,Cristiana Libardi
Silva,Priscila Vendramini
Guimarães,Marta Fonseca Martins
Serão,Nicola Vergara Lopes
Guimarães,José Domingos
Guimarães,Simone Eliza Facioni
Differential expression of genes in follicular cells of swines
author_facet Miranda-Furtado,Cristiana Libardi
Silva,Priscila Vendramini
Guimarães,Marta Fonseca Martins
Serão,Nicola Vergara Lopes
Guimarães,José Domingos
Guimarães,Simone Eliza Facioni
author_sort Miranda-Furtado,Cristiana Libardi
title Differential expression of genes in follicular cells of swines
title_short Differential expression of genes in follicular cells of swines
title_full Differential expression of genes in follicular cells of swines
title_fullStr Differential expression of genes in follicular cells of swines
title_full_unstemmed Differential expression of genes in follicular cells of swines
title_sort differential expression of genes in follicular cells of swines
description The main purpose of the present study was to identify for candidate genes related to ovulation in swines. To do so, it was investigated in ovarian follicular cells through quantitative real-time PCR the differential expression of the following genes: steroidogenic acute regulator (STAR), GATA-binding protein 4 (GATA), prostaglandin F2α (PGF2α), progesterone receptor (P4R), follicle-stimulating hormone receptor (FSHR), and cytochrome P450 aromatase (CYP19). These genes encode hormone receptors (FSHR and P4R), hormone (PGF2α), steroidogenic proteins (STAR and CYP19) and transcription factor (GATA). Folicular cells were collected from sows with high and low number of piglets/litters during the follicular phase of the estrus cycle. There was difference in transcript abundance among low and high prolific sows for the STAR, GATA, PGF2α, P4R and CYP19 genes. For the FSHR gene, the fold change was not considered to be significantly different. Because in the present study only the transcript level of the above mentioned genes was analyzed, no inference can be made regarded to protein translation or activity. Therefore, gene sequence trials and other functional studies will be necessary to complement the present results, allowing a better understanding on biological complexity of these genes and their use as markers for prolificity in swines.
publisher Sociedade Brasileira de Zootecnia
publishDate 2010
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-35982010000500012
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