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Correlation Networks Provide New Insights into the Architecture of Testicular Steroid Pathways in Pigs

Steroid metabolism is a fundamental process in the porcine testis to provide testosterone but also estrogens and androstenone, which are essential for the physiology of the boar. This study concerns boars at an early stage of puberty. Using a RT-qPCR approach, we showed that the transcriptional acti...

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Autores principales: Robic, Annie, Faraut, Thomas, Feve, Katia, Djebali, Sarah, Prunier, Armelle, Larzul, Catherine, Liaubet, Laurence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8069258/
https://www.ncbi.nlm.nih.gov/pubmed/33918852
http://dx.doi.org/10.3390/genes12040551
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author Robic, Annie
Faraut, Thomas
Feve, Katia
Djebali, Sarah
Prunier, Armelle
Larzul, Catherine
Liaubet, Laurence
author_facet Robic, Annie
Faraut, Thomas
Feve, Katia
Djebali, Sarah
Prunier, Armelle
Larzul, Catherine
Liaubet, Laurence
author_sort Robic, Annie
collection PubMed
description Steroid metabolism is a fundamental process in the porcine testis to provide testosterone but also estrogens and androstenone, which are essential for the physiology of the boar. This study concerns boars at an early stage of puberty. Using a RT-qPCR approach, we showed that the transcriptional activities of several genes providing key enzymes involved in this metabolism (such as CYP11A1) are correlated. Surprisingly, HSD17B3, a key gene for testosterone production, was absent from this group. An additional weighted gene co-expression network analysis was performed on two large sets of mRNA-seq to identify co-expression modules. Of these modules, two containing either CYP11A1 or HSD17B3 were further analyzed. This comprehensive correlation meta-analysis identified a group of 85 genes with CYP11A1 as hub gene, but did not allow the characterization of a robust correlation network around HSD17B3. As the CYP11A1-group includes most of the genes involved in steroid synthesis pathways (including LHCGR encoding for the LH receptor), it may control the synthesis of most of the testicular steroids. The independent expression of HSD17B3 probably allows part of the production of testosterone to escape this control. This CYP11A1-group contained also INSL3 and AGT genes encoding a peptide hormone and an angiotensin peptide precursor, respectively.
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spelling pubmed-80692582021-04-26 Correlation Networks Provide New Insights into the Architecture of Testicular Steroid Pathways in Pigs Robic, Annie Faraut, Thomas Feve, Katia Djebali, Sarah Prunier, Armelle Larzul, Catherine Liaubet, Laurence Genes (Basel) Article Steroid metabolism is a fundamental process in the porcine testis to provide testosterone but also estrogens and androstenone, which are essential for the physiology of the boar. This study concerns boars at an early stage of puberty. Using a RT-qPCR approach, we showed that the transcriptional activities of several genes providing key enzymes involved in this metabolism (such as CYP11A1) are correlated. Surprisingly, HSD17B3, a key gene for testosterone production, was absent from this group. An additional weighted gene co-expression network analysis was performed on two large sets of mRNA-seq to identify co-expression modules. Of these modules, two containing either CYP11A1 or HSD17B3 were further analyzed. This comprehensive correlation meta-analysis identified a group of 85 genes with CYP11A1 as hub gene, but did not allow the characterization of a robust correlation network around HSD17B3. As the CYP11A1-group includes most of the genes involved in steroid synthesis pathways (including LHCGR encoding for the LH receptor), it may control the synthesis of most of the testicular steroids. The independent expression of HSD17B3 probably allows part of the production of testosterone to escape this control. This CYP11A1-group contained also INSL3 and AGT genes encoding a peptide hormone and an angiotensin peptide precursor, respectively. MDPI 2021-04-09 /pmc/articles/PMC8069258/ /pubmed/33918852 http://dx.doi.org/10.3390/genes12040551 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Robic, Annie
Faraut, Thomas
Feve, Katia
Djebali, Sarah
Prunier, Armelle
Larzul, Catherine
Liaubet, Laurence
Correlation Networks Provide New Insights into the Architecture of Testicular Steroid Pathways in Pigs
title Correlation Networks Provide New Insights into the Architecture of Testicular Steroid Pathways in Pigs
title_full Correlation Networks Provide New Insights into the Architecture of Testicular Steroid Pathways in Pigs
title_fullStr Correlation Networks Provide New Insights into the Architecture of Testicular Steroid Pathways in Pigs
title_full_unstemmed Correlation Networks Provide New Insights into the Architecture of Testicular Steroid Pathways in Pigs
title_short Correlation Networks Provide New Insights into the Architecture of Testicular Steroid Pathways in Pigs
title_sort correlation networks provide new insights into the architecture of testicular steroid pathways in pigs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8069258/
https://www.ncbi.nlm.nih.gov/pubmed/33918852
http://dx.doi.org/10.3390/genes12040551
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