Characterization of DNA Methylation Patterns and Mining of Epigenetic Markers During Genomic Reprogramming in SCNT Embryos

Bibliographic Details
Title: Characterization of DNA Methylation Patterns and Mining of Epigenetic Markers During Genomic Reprogramming in SCNT Embryos
Authors: Pengbo Cao, Hanshuang Li, Yongchun Zuo, Buhe Nashun
Source: Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Publisher Information: Frontiers Media S.A., 2020.
Publication Year: 2020
Collection: LCC:Biology (General)
Subject Terms: DNA methylation, SCNT, WGCNA, epigenetic reprogramming, ZGA, Biology (General), QH301-705.5
More Details: Somatic cell nuclear transfer (SCNT), also known as somatic cell cloning, is a commonly used technique to study epigenetic reprogramming. Although SCNT has the advantages of being safe and able to obtain pluripotent cells, early developmental arrest happens in most SCNT embryos. Overcoming epigenetic barriers is currently the primary strategy for improving reprogramming efficiency and improving developmental rate in SCNT embryos. In this study, we analyzed DNA methylation profiles of in vivo fertilized embryos and SCNT embryos with different developmental fates. Overall DNA methylation level was higher in SCNT embryos during global de-methylation process compared to in vivo fertilized embryos. In addition, promoter region, first intron and 3′UTR were found to be the major genomic regions that were hyper-methylated in SCNT embryos. Surprisingly, we found the length of re-methylated region was directly related to the change of methylation level. Furthermore, a number of genes including Dppa2 and Dppa4 which are important for early zygotic genome activation (ZGA) were not properly activated in SCNT embryos. This study comprehensively analyzed genome-wide DNA methylation patterns in SCNT embryos and provided candidate target genes for improving efficiency of genomic reprogramming in SCNT embryos. Since SCNT technology has been widely used in agricultural and pastoral production, protection of endangered animals, and therapeutic cloning, the findings of this study have significant importance for all these fields.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2296-634X
Relation: https://www.frontiersin.org/article/10.3389/fcell.2020.570107/full; https://doaj.org/toc/2296-634X
DOI: 10.3389/fcell.2020.570107
Access URL: https://doaj.org/article/c62d1f7dd54d4f3788cbb6033ac2a0b1
Accession Number: edsdoj.62d1f7dd54d4f3788cbb6033ac2a0b1
Database: Directory of Open Access Journals
More Details
ISSN:2296634X
DOI:10.3389/fcell.2020.570107
Published in:Frontiers in Cell and Developmental Biology
Language:English