| Literature DB >> 25307438 |
Azizollah Bakhtari1, Hamid-Reza Rahmani1, Elham Bonakdar1, Farnoosh Jafarpour2, Vajiheh Asgari2, Sayyed-Mortaza Hosseini2, Mehdi Hajian2, Mohammad-Ali Edriss1, Mohammad-Hossein Nasr-Esfahani3.
Abstract
Appropriate epigenetic changes in preimplantation embryos are critical for embryonic development and successful pregnancy. The aim of this study was to evaluate the effects of some assisted reproductive techniques (ARTs) on a panel of epigenetic biomarkers by immunofluorescence staining at blastocyst stage. For this purpose, four treatment groups were designed: control (C), superovulation (S), superovulation+in vitro culture (SI), and superovulation+vitrification+in vitro culture (SVI). Results showed that vitrification decreased the developmental competence of embryos cultured in vitro (P<0.05). Semi-quantitative analysis revealed that vitrification decreased the fluorescence intensity of global DNA methylation in the inner cell mass (ICM), in SVI Group in comparison to C group (P<0.05). Superovulation, elevated the level of H3K9acetylation of trophectoderm (TE) in comparison to C and SI groups (P<0.05). Furthermore, ARTs manipulations influenced H3K9acetylation in the ICM (P<0.05). The fluorescence intensity of H4K12acetylation in TE for SVI group was higher than C and S (P<0.05). For H3K4tri-methylation, S group had higher fluorescence intensity in the ICM in comparison to SI and SVI (P<0.05). Finally, in vitro culture decreased Pou5f1 protein signal in comparison to in vivo-derived embryos at blastocyst stage (P<0.05). In conclusion, ART manipulations may have important influences on multiple epigenetic biomarkers.Entities:
Keywords: ART manipulations; DNA methylation; H3K4 tri-methylation; H3K9 acetylation; H4K12 acetylation; Pou5f1
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Year: 2014 PMID: 25307438 DOI: 10.1016/j.cryobiol.2014.09.379
Source DB: PubMed Journal: Cryobiology ISSN: 0011-2240 Impact factor: 2.487