Oxygen concentration affects de novo DNA methylation and transcription in in vitro cultured oocytes.


Journal

Clinical epigenetics
ISSN: 1868-7083
Titre abrégé: Clin Epigenetics
Pays: Germany
ID NLM: 101516977

Informations de publication

Date de publication:
28 06 2021
Historique:
received: 12 03 2021
accepted: 15 06 2021
entrez: 29 6 2021
pubmed: 30 6 2021
medline: 27 1 2022
Statut: epublish

Résumé

Reproductive biology methods rely on in vitro follicle cultures from mature follicles obtained by hormonal stimulation for generating metaphase II oocytes to be fertilised and developed into a healthy embryo. Such techniques are used routinely in both rodent and human species. DNA methylation is a dynamic process that plays a role in epigenetic regulation of gametogenesis and development. In mammalian oocytes, DNA methylation establishment regulates gene expression in the embryos. This regulation is particularly important for a class of genes, imprinted genes, whose expression patterns are crucial for the next generation. The aim of this work was to establish an in vitro culture system for immature mouse oocytes that will allow manipulation of specific factors for a deeper analysis of regulatory mechanisms for establishing transcription regulation-associated methylation patterns. An in vitro culture system was developed from immature mouse oocytes that were grown to germinal vesicles (GV) under two different conditions: normoxia (20% oxygen, 20% O Our observations reveal changes in DNA methylation and transcripts between oocytes cultured in vitro with different oxygen concentrations and in vivo-grown murine oocytes. Oocytes grown under 20% O

Sections du résumé

BACKGROUND
Reproductive biology methods rely on in vitro follicle cultures from mature follicles obtained by hormonal stimulation for generating metaphase II oocytes to be fertilised and developed into a healthy embryo. Such techniques are used routinely in both rodent and human species. DNA methylation is a dynamic process that plays a role in epigenetic regulation of gametogenesis and development. In mammalian oocytes, DNA methylation establishment regulates gene expression in the embryos. This regulation is particularly important for a class of genes, imprinted genes, whose expression patterns are crucial for the next generation. The aim of this work was to establish an in vitro culture system for immature mouse oocytes that will allow manipulation of specific factors for a deeper analysis of regulatory mechanisms for establishing transcription regulation-associated methylation patterns.
RESULTS
An in vitro culture system was developed from immature mouse oocytes that were grown to germinal vesicles (GV) under two different conditions: normoxia (20% oxygen, 20% O
CONCLUSIONS
Our observations reveal changes in DNA methylation and transcripts between oocytes cultured in vitro with different oxygen concentrations and in vivo-grown murine oocytes. Oocytes grown under 20% O

Identifiants

pubmed: 34183052
doi: 10.1186/s13148-021-01116-3
pii: 10.1186/s13148-021-01116-3
pmc: PMC8240245
doi:

Substances chimiques

Oxygen S88TT14065

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

132

Subventions

Organisme : Biotieteiden ja Ympäristön Tutkimuksen Toimikunta
ID : 243014583
Organisme : Swedish Insitute
Organisme : Medical Research Council
ID : MR/K011332/1
Pays : United Kingdom
Organisme : Academy of Finland
ID : 311934
Organisme : Biotechnology and Biological Sciences Research Council
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0800013
Pays : United Kingdom

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Auteurs

Florence Naillat (F)

Epigenetics Program, Babraham Institute, Cambridge, CB22 3AT, UK. Florence.naillat@oulu.fi.
Diseases Network Research Unit, Faculty of Biochemistry and Molecular Medicine, Oulu University, Oulu, Finland. Florence.naillat@oulu.fi.

Heba Saadeh (H)

Epigenetics Program, Babraham Institute, Cambridge, CB22 3AT, UK.
Department of Computer Science, King Abdullah II School of Information Technology, The University of Jordan, Amman, Jordan.

Joanna Nowacka-Woszuk (J)

Epigenetics Program, Babraham Institute, Cambridge, CB22 3AT, UK.
Department of Genetics and Animal Breeding, Poznan University of Life Sciences, Poznan, Poland.

Lenka Gahurova (L)

Epigenetics Program, Babraham Institute, Cambridge, CB22 3AT, UK.
Laboratory of Early Mammalian Development, Department of Molecular Biology and Genetics, University of South Bohemia, 37005, České Budějovice, Czech Republic.

Fatima Santos (F)

Epigenetics Program, Babraham Institute, Cambridge, CB22 3AT, UK.

Shin-Ichi Tomizawa (SI)

Epigenetics Program, Babraham Institute, Cambridge, CB22 3AT, UK.
School of Medicine, Yokohama City University, Yokohama, Japan.

Gavin Kelsey (G)

Epigenetics Program, Babraham Institute, Cambridge, CB22 3AT, UK. gavin.kelsey@babraham.ac.uk.
Centre for Trophoblast Research, University of Cambridge, Cambridge, CB2 3EG, UK. gavin.kelsey@babraham.ac.uk.

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