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High-fat diet-induced and genetically inherited obesity differentially alters DNA methylation profile in the germline of adult male rats

BACKGROUND: Paternal obesity has been associated with reduced live birth rates. It could lead to inheritance of metabolic disturbances to the offspring through epigenetic mechanisms. However, obesity is a multifactorial disorder with genetic or environmental causes. Earlier we had demonstrated diffe...

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Autores principales: Deshpande, Sharvari S., Nemani, Harishankar, Arumugam, Gandhimathi, Ravichandran, Avinash, Balasinor, Nafisa H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7678167/
https://www.ncbi.nlm.nih.gov/pubmed/33213487
http://dx.doi.org/10.1186/s13148-020-00974-7
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author Deshpande, Sharvari S.
Nemani, Harishankar
Arumugam, Gandhimathi
Ravichandran, Avinash
Balasinor, Nafisa H.
author_facet Deshpande, Sharvari S.
Nemani, Harishankar
Arumugam, Gandhimathi
Ravichandran, Avinash
Balasinor, Nafisa H.
author_sort Deshpande, Sharvari S.
collection PubMed
description BACKGROUND: Paternal obesity has been associated with reduced live birth rates. It could lead to inheritance of metabolic disturbances to the offspring through epigenetic mechanisms. However, obesity is a multifactorial disorder with genetic or environmental causes. Earlier we had demonstrated differential effects of high-fat diet-induced obesity (DIO) and genetically inherited obesity (GIO) on metabolic, hormonal profile, male fertility, and spermatogenesis using two rat models. The present study aimed to understand the effect of DIO and GIO on DNA methylation in male germline, and its subsequent effects on the resorbed (post-implantation embryo loss) and normal embryos. First, we assessed the DNA methylation enzymatic machinery in the testis by Real-Time PCR, followed global DNA methylation levels in spermatozoa and testicular cells by ELISA and flow cytometry, respectively. Further, we performed Methylation Sequencing in spermatozoa for both the groups. Sequencing data in spermatozoa from both the groups were validated using Pyrosequencing. Expression of the differentially methylated genes was assessed in the resorbed and normal embryos sired by the DIO group using Real-Time PCR for functional validation. RESULTS: We noted a significant decrease in Dnmt transcript and global DNA methylation levels in the DIO group and an increase in the GIO group. Sequencing analysis showed 16,966 and 9113 differentially methylated regions in the spermatozoa of the DIO and GIO groups, respectively. Upon pathway analysis, we observed genes enriched in pathways involved in embryo growth and development namely Wnt, Hedgehog, TGF-beta, and Notch in spermatozoa for both the groups, the methylation status of which partially correlated with the gene expression pattern in resorbed and normal embryos sired by the DIO group. CONCLUSION: Our study reports the mechanism by which diet-induced and genetically inherited obesity causes differential effects on the DNA methylation in the male germline that could be due to a difference in the white adipose tissue accumulation. These differences could either lead to embryo loss or transmit obesity-related traits to the offspring in adult life.
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spelling pubmed-76781672020-11-20 High-fat diet-induced and genetically inherited obesity differentially alters DNA methylation profile in the germline of adult male rats Deshpande, Sharvari S. Nemani, Harishankar Arumugam, Gandhimathi Ravichandran, Avinash Balasinor, Nafisa H. Clin Epigenetics Research BACKGROUND: Paternal obesity has been associated with reduced live birth rates. It could lead to inheritance of metabolic disturbances to the offspring through epigenetic mechanisms. However, obesity is a multifactorial disorder with genetic or environmental causes. Earlier we had demonstrated differential effects of high-fat diet-induced obesity (DIO) and genetically inherited obesity (GIO) on metabolic, hormonal profile, male fertility, and spermatogenesis using two rat models. The present study aimed to understand the effect of DIO and GIO on DNA methylation in male germline, and its subsequent effects on the resorbed (post-implantation embryo loss) and normal embryos. First, we assessed the DNA methylation enzymatic machinery in the testis by Real-Time PCR, followed global DNA methylation levels in spermatozoa and testicular cells by ELISA and flow cytometry, respectively. Further, we performed Methylation Sequencing in spermatozoa for both the groups. Sequencing data in spermatozoa from both the groups were validated using Pyrosequencing. Expression of the differentially methylated genes was assessed in the resorbed and normal embryos sired by the DIO group using Real-Time PCR for functional validation. RESULTS: We noted a significant decrease in Dnmt transcript and global DNA methylation levels in the DIO group and an increase in the GIO group. Sequencing analysis showed 16,966 and 9113 differentially methylated regions in the spermatozoa of the DIO and GIO groups, respectively. Upon pathway analysis, we observed genes enriched in pathways involved in embryo growth and development namely Wnt, Hedgehog, TGF-beta, and Notch in spermatozoa for both the groups, the methylation status of which partially correlated with the gene expression pattern in resorbed and normal embryos sired by the DIO group. CONCLUSION: Our study reports the mechanism by which diet-induced and genetically inherited obesity causes differential effects on the DNA methylation in the male germline that could be due to a difference in the white adipose tissue accumulation. These differences could either lead to embryo loss or transmit obesity-related traits to the offspring in adult life. BioMed Central 2020-11-19 /pmc/articles/PMC7678167/ /pubmed/33213487 http://dx.doi.org/10.1186/s13148-020-00974-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Deshpande, Sharvari S.
Nemani, Harishankar
Arumugam, Gandhimathi
Ravichandran, Avinash
Balasinor, Nafisa H.
High-fat diet-induced and genetically inherited obesity differentially alters DNA methylation profile in the germline of adult male rats
title High-fat diet-induced and genetically inherited obesity differentially alters DNA methylation profile in the germline of adult male rats
title_full High-fat diet-induced and genetically inherited obesity differentially alters DNA methylation profile in the germline of adult male rats
title_fullStr High-fat diet-induced and genetically inherited obesity differentially alters DNA methylation profile in the germline of adult male rats
title_full_unstemmed High-fat diet-induced and genetically inherited obesity differentially alters DNA methylation profile in the germline of adult male rats
title_short High-fat diet-induced and genetically inherited obesity differentially alters DNA methylation profile in the germline of adult male rats
title_sort high-fat diet-induced and genetically inherited obesity differentially alters dna methylation profile in the germline of adult male rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7678167/
https://www.ncbi.nlm.nih.gov/pubmed/33213487
http://dx.doi.org/10.1186/s13148-020-00974-7
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