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PMID: 21802491 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Is DNA methylation an epigenetic contribution to transcriptional regulation of the bovine endometrium during the estrous cycle and early pregnancy?

Molecular and cellular endocrinology ·Vol. 348 ·No. 1 ·2012-01-02 ·Pages 67-77

Fürst RW, Meyer HH, Schweizer G, Ulbrich SE

Abstract

Epigenetic events controlling the transcriptional regulation of genes involved in endometrial function during the estrous cycle and early pregnancy have only sparsely been investigated. We analyzed the gene expression of DNA methyltransferases and the most prominent endocrine transcriptional mediator estrogen receptor alpha (ESR1) in the bovine endometrium of heifers at 0, 12 and 18 days following estrous and at day 18 after insemination. The luminometric methylation assay for the investigation of global DNA methylation and an elegant combination of methylation-sensitive high resolution melting and pyrosequencing for local methylation levels of ESR1 were deployed. In spite of differential gene expression of ESR1 among groups, no differences in endometrial ESR1 DNA methylation during neither estrous cycle nor early pregnancy were determined. Global DNA methylation prevailed at similar low levels in endometrium, likely controlled by the observed moderate DNMT3b expression. Thus, the epigenetic contribution of DNA methylation influencing endometrial function seems rather limited. However, because a control tissue expressing only minute amounts of ESR1 transcripts was locally significantly higher methylated, DNA methylation might contribute to an appropriate tissue-specific expression status underlying further specific control mechanisms of gene transcription.

MeSH Terms
Animals Cattle DNA Methylation DNA Modification Methylases/genetics,metabolism Endometrium/metabolism Epigenesis, Genetic Estrogen Receptor alpha/genetics,metabolism Estrous Cycle Female Gene Expression Polymerase Chain Reaction Pregnancy Pregnancy, Animal/genetics,metabolism RNA, Messenger/metabolism Regression Analysis Sequence Analysis, DNA/methods Transcription, Genetic Transition Temperature
Chemicals
Estrogen Receptor alpha RNA, Messenger DNA Modification Methylases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Fürst Rainer W
Physiology Weihenstephan, Technische Universität München, 85354 Freising-Weihenstephan, Germany.
Meyer Heinrich H D
Schweizer Günther
Ulbrich Susanne E
Article Info
Journal
Molecular and cellular endocrinology
Abbr.
Mol Cell Endocrinol
ISSN
1872-8057
Published
2012-01-02
Epub
2011-00-23
Pages
67-77
Language
English
Region
Ireland
NLM ID
7500844
Subset
IM
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