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Reproduction, Fertility and Development Reproduction, Fertility and Development Society
Vertebrate reproductive science and technology
RESEARCH ARTICLE

Methylation of progesterone receptor isoform A and B promoters in the reproductive system of cows

Robert Rekawiecki A B , Katarzyna Kisielewska A , Magdalena K. Kowalik A and Jan Kotwica A
+ Author Affiliations
- Author Affiliations

A Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, Tuwima 10, 10-748 Olsztyn, Poland.

B Corresponding author. Email: r.rekawiecki@pan.olsztyn.pl

Reproduction, Fertility and Development 30(12) 1634-1642 https://doi.org/10.1071/RD17518
Submitted: 19 December 2017  Accepted: 5 May 2018   Published: 14 June 2018

Abstract

The aim of this study was to investigate whether the promoters of progesterone receptor isoform A (PGRA) and B (PGRB) are methylated and to determine the percentage of methylation occurring for each isoform. Genomic DNA was isolated from the corpora lutea (CL) and endometrial slices from cows on Days 2–5, 6–10, 11–16 and 17–20 of the oestrous cycle. DNA was bisulphite-converted and amplified using methyl-specific polymerase chain reaction (PCR) with primers that detect both methylated and unmethylated sequences. The determination of the percentage of the methylation was performed using HpaII and MspI restriction enzymes. Methyl-specific PCR showed partial methylation of PGRA and PGRB promoters in the CL and endometrium during the oestrous cycle. Methylation for PGRA was between 15 and 17% and for PGRB was in the range of 6 to 7.7% during the oestrous cycle in the CL. In the endometrium, the methylation for PGRA was between 6 and 7.3% and for PGRB was between 3 and 4.8% during the oestrous cycle. The data obtained indicate that the higher promoter methylation of the PGRA isoform could be a mechanism for regulation of PGRA inhibitory activity against PGRB and, in this way, methylation may influence the regulation of progesterone action in the CL and endometrium.

Additional keywords: corpus luteum, endometrium, nuclear receptors.


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