Sex-specific epigenetic profile of inner cell mass of mice conceived in vivo or by IVF. (3rd October 2020)
- Record Type:
- Journal Article
- Title:
- Sex-specific epigenetic profile of inner cell mass of mice conceived in vivo or by IVF. (3rd October 2020)
- Main Title:
- Sex-specific epigenetic profile of inner cell mass of mice conceived in vivo or by IVF
- Authors:
- Ruggeri, Elena
Lira-Albarrán, Saúl
Grow, Edward J
Liu, Xiaowei
Harner, Royce
Maltepe, Emin
Ramalho-Santos, Miguel
Donjacour, Annemarie
Rinaudo, Paolo - Abstract:
- Abstract: The preimplantation stage of development is exquisitely sensitive to environmental stresses, and changes occurring during this developmental phase may have long-term health effects. Animal studies indicate that IVF offspring display metabolic alterations, including hypertension, glucose intolerance and cardiac hypertrophy, often in a sexual dimorphic fashion. The detailed nature of epigenetic changes following in-vitro culture is, however, unknown. This study was performed to evaluate the epigenetic (using whole-genome bisulfite sequencing (WGBS) and assay for transposase-accessible chromatin using sequencing (ATAC-seq)) and transcriptomic changes (using RNA-seq) occurring in the inner cell mass (ICM) of male or female mouse embryos generated in vivo or by IVF. We found that the ICM of IVF embryos, compared to the in-vivo ICM, differed in 3% of differentially methylated regions (DMRs), of which 0.1% were located on CpG islands. ATAC-seq revealed that 293 regions were more accessible and 101 were less accessible in IVF embryos, while RNA-seq revealed that 21 genes were differentially regulated in IVF embryos. Functional enrichment analysis revealed that stress signalling (STAT and NF-kB signalling), developmental processes and cardiac hypertrophy signalling showed consistent changes in WGBS and ATAC-seq platforms. In contrast, male and female embryos showed minimal changes. Male ICM had an increased number of significantly hyper-methylated DMRs, while only 27Abstract: The preimplantation stage of development is exquisitely sensitive to environmental stresses, and changes occurring during this developmental phase may have long-term health effects. Animal studies indicate that IVF offspring display metabolic alterations, including hypertension, glucose intolerance and cardiac hypertrophy, often in a sexual dimorphic fashion. The detailed nature of epigenetic changes following in-vitro culture is, however, unknown. This study was performed to evaluate the epigenetic (using whole-genome bisulfite sequencing (WGBS) and assay for transposase-accessible chromatin using sequencing (ATAC-seq)) and transcriptomic changes (using RNA-seq) occurring in the inner cell mass (ICM) of male or female mouse embryos generated in vivo or by IVF. We found that the ICM of IVF embryos, compared to the in-vivo ICM, differed in 3% of differentially methylated regions (DMRs), of which 0.1% were located on CpG islands. ATAC-seq revealed that 293 regions were more accessible and 101 were less accessible in IVF embryos, while RNA-seq revealed that 21 genes were differentially regulated in IVF embryos. Functional enrichment analysis revealed that stress signalling (STAT and NF-kB signalling), developmental processes and cardiac hypertrophy signalling showed consistent changes in WGBS and ATAC-seq platforms. In contrast, male and female embryos showed minimal changes. Male ICM had an increased number of significantly hyper-methylated DMRs, while only 27 regions showed different chromatin accessibility and only one gene was differentially expressed. In summary, this study provides the first comprehensive analysis of DNA methylation, chromatin accessibility and RNA expression changes induced by IVF in male and female ICMs. This dataset can be of value to all researchers interested in the developmental origin of health and disease (DOHaD) hypothesis and might lead to a better understanding of how early embryonic manipulation may affect adult health. … (more)
- Is Part Of:
- Molecular human reproduction. Volume 26:Number 11(2020)
- Journal:
- Molecular human reproduction
- Issue:
- Volume 26:Number 11(2020)
- Issue Display:
- Volume 26, Issue 11 (2020)
- Year:
- 2020
- Volume:
- 26
- Issue:
- 11
- Issue Sort Value:
- 2020-0026-0011-0000
- Page Start:
- 866
- Page End:
- 878
- Publication Date:
- 2020-10-03
- Subjects:
- IVF -- DOHaD -- epigenetics -- in-vitro culture -- preimplantation embryo
Human reproduction -- Molecular aspects -- Periodicals
Electronic journals
612.6 - Journal URLs:
- http://molehr.oxfordjournals.org ↗
http://molehr.oxfordjournals.org/archive ↗
http://molehr.oxfordjournals.org/archive ↗
http://www.ingentaconnect.com/content/oup/molehr ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/molehr/gaaa064 ↗
- Languages:
- English
- ISSNs:
- 1360-9947
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817650
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21686.xml