Back to Search
Start Over
Progesterone Receptor B Promoter Hypermethylation in Human Placenta After Labor Onset
- Source :
- Reproductive Sciences. 22:335-342
- Publication Year :
- 2015
- Publisher :
- Springer Science and Business Media LLC, 2015.
-
Abstract
- To determine the methylation status of progesterone receptor B (PR-B) promoter and how PR-B regulates progesterone action in placenta during human pregnancy. Placentas were obtained from the pregnancy women at term who underwent cesarean delivery and vaginal delivery. The methylation status of the PR-B promoter was analyzed using the methylation-specific polymerase chain reaction (PCR) and bisulfite sequencing PCR. And the messenger RNA (mRNA) and protein expression of the PR-B and DNA methyltransferases (DNMTs) were determined by quantitative real-time PCR and Western blot. Compared with the cesarean group, the placentas of vaginal delivery group had greater levels of PR-B DNA methylation, and the PR-B, DNMT1, DNMT3a, and DNMT3b mRNA and protein expression were significantly decreased. Progesterone receptor B methylation occurs with high frequency after labor onset and may play an important epigenetic mechanism of labor-related PR-B negative expression, thereby mediating the biological process of functional progesterone withdrawal at term for parturition.
- Subjects :
- Adult
DNA (Cytosine-5-)-Methyltransferase 1
Progesterone receptor B
Methyltransferase
Blotting, Western
Bisulfite sequencing
Biology
Real-Time Polymerase Chain Reaction
DNA Methyltransferase 3A
Epigenesis, Genetic
Andrology
Pregnancy
Placenta
medicine
Humans
DNA (Cytosine-5-)-Methyltransferases
RNA, Messenger
Promoter Regions, Genetic
Messenger RNA
Labor, Obstetric
Reverse Transcriptase Polymerase Chain Reaction
Obstetrics and Gynecology
Methylation
DNA Methylation
medicine.disease
medicine.anatomical_structure
Gene Expression Regulation
embryonic structures
DNA methylation
Female
Receptors, Progesterone
Subjects
Details
- ISSN :
- 19337205 and 19337191
- Volume :
- 22
- Database :
- OpenAIRE
- Journal :
- Reproductive Sciences
- Accession number :
- edsair.doi.dedup.....5ff8873e099d4cfbd352ed7eb1c1d46d