Effect of TET inhibitor on bovine parthenogenetic embryo development.

DNA demethylation catalysed by the ten-eleven translocation (TET) protein is an important step during extensive global epigenetic reprogramming in mammals. However, whether TET proteins play a key role in DNA demethylation during the development of bovine pre-implanted embryos is still unclear. In t...

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Main Authors: Jian Zhang, Sheng Zhang, Yutian Wang, Hui Cheng, Linlin Hao, Yanhui Zhai, Zhiren Zhang, Xinglan An, Xiaoling Ma, Xueming Zhang, Ziyi Li, Bo Tang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5739418?pdf=render
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author Jian Zhang
Sheng Zhang
Yutian Wang
Hui Cheng
Linlin Hao
Yanhui Zhai
Zhiren Zhang
Xinglan An
Xiaoling Ma
Xueming Zhang
Ziyi Li
Bo Tang
author_facet Jian Zhang
Sheng Zhang
Yutian Wang
Hui Cheng
Linlin Hao
Yanhui Zhai
Zhiren Zhang
Xinglan An
Xiaoling Ma
Xueming Zhang
Ziyi Li
Bo Tang
author_sort Jian Zhang
collection DOAJ
description DNA demethylation catalysed by the ten-eleven translocation (TET) protein is an important step during extensive global epigenetic reprogramming in mammals. However, whether TET proteins play a key role in DNA demethylation during the development of bovine pre-implanted embryos is still unclear. In this study, we utilized dimethyloxallyl glycine (DMOG), a small-molecule inhibitor of the TET protein, to impede the enzymatic activity of TET and explore subsequent effects on bovine parthenogenetic embryo development. We first detected the expression of the TET family, consisting of TET1, TET2 and TET3, in bovine MII stage oocytes and found that TET3 is more highly expressed than TET1 and TET2. Treatment with 1 mM DMOG increased 5mC levels (30.4% vs 79.8% at the 8-cell stage for satellite I, 25.3% vs 40.6% at the 8-cell stage for α-satellite, 20.5% vs 73.5% at the blastocyst stage for satellite I and 16.6% vs 30.0% at the blastocyst stage for α-satellite) at every bovine parthenogenetic embryo developmental stage. At the same time, DNA methylation level of satellite DNA and pluripotency gene promoters increased significantly. Real-time PCR analysis results indicated that the transcription levels of NANOG and OCT-4 decreased in the DMOG-treated group. Furthermore, TET inhibition negatively affected blastocyst formation, resulting in a decline in the blastocyst rate (17.1 ± 1.3% vs 24.1 ± 0.6%); however, the percentage of apoptotic cells was significantly increased according to the results of a TUNEL assay. Additionally, expression levels of the apoptosis-related gene BAX were up-regulated, while the expression of BCL-2 was down-regulated. In conclusion, these results support that TET plays important roles in bovine parthenogenetic embryo development by influencing DNA methylation reprogramming, gene expression and apoptosis.
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spelling doaj.art-70ff51d28820414898bde996ce11dfa22022-12-21T18:59:33ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-011212e018954210.1371/journal.pone.0189542Effect of TET inhibitor on bovine parthenogenetic embryo development.Jian ZhangSheng ZhangYutian WangHui ChengLinlin HaoYanhui ZhaiZhiren ZhangXinglan AnXiaoling MaXueming ZhangZiyi LiBo TangDNA demethylation catalysed by the ten-eleven translocation (TET) protein is an important step during extensive global epigenetic reprogramming in mammals. However, whether TET proteins play a key role in DNA demethylation during the development of bovine pre-implanted embryos is still unclear. In this study, we utilized dimethyloxallyl glycine (DMOG), a small-molecule inhibitor of the TET protein, to impede the enzymatic activity of TET and explore subsequent effects on bovine parthenogenetic embryo development. We first detected the expression of the TET family, consisting of TET1, TET2 and TET3, in bovine MII stage oocytes and found that TET3 is more highly expressed than TET1 and TET2. Treatment with 1 mM DMOG increased 5mC levels (30.4% vs 79.8% at the 8-cell stage for satellite I, 25.3% vs 40.6% at the 8-cell stage for α-satellite, 20.5% vs 73.5% at the blastocyst stage for satellite I and 16.6% vs 30.0% at the blastocyst stage for α-satellite) at every bovine parthenogenetic embryo developmental stage. At the same time, DNA methylation level of satellite DNA and pluripotency gene promoters increased significantly. Real-time PCR analysis results indicated that the transcription levels of NANOG and OCT-4 decreased in the DMOG-treated group. Furthermore, TET inhibition negatively affected blastocyst formation, resulting in a decline in the blastocyst rate (17.1 ± 1.3% vs 24.1 ± 0.6%); however, the percentage of apoptotic cells was significantly increased according to the results of a TUNEL assay. Additionally, expression levels of the apoptosis-related gene BAX were up-regulated, while the expression of BCL-2 was down-regulated. In conclusion, these results support that TET plays important roles in bovine parthenogenetic embryo development by influencing DNA methylation reprogramming, gene expression and apoptosis.http://europepmc.org/articles/PMC5739418?pdf=render
spellingShingle Jian Zhang
Sheng Zhang
Yutian Wang
Hui Cheng
Linlin Hao
Yanhui Zhai
Zhiren Zhang
Xinglan An
Xiaoling Ma
Xueming Zhang
Ziyi Li
Bo Tang
Effect of TET inhibitor on bovine parthenogenetic embryo development.
PLoS ONE
title Effect of TET inhibitor on bovine parthenogenetic embryo development.
title_full Effect of TET inhibitor on bovine parthenogenetic embryo development.
title_fullStr Effect of TET inhibitor on bovine parthenogenetic embryo development.
title_full_unstemmed Effect of TET inhibitor on bovine parthenogenetic embryo development.
title_short Effect of TET inhibitor on bovine parthenogenetic embryo development.
title_sort effect of tet inhibitor on bovine parthenogenetic embryo development
url http://europepmc.org/articles/PMC5739418?pdf=render
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