The asynchronous establishment of chromatin 3D architecture between in vitro fertilized and uniparental preimplantation pig embryos

Abstract Background Pigs are important animals for agricultural and biomedical research, and improvement is needed for use of the assisted reproductive technologies. Determining underlying mechanisms of epigenetic reprogramming in the early stage of preimplantation embryos derived from in vitro fert...

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Main Authors: Feifei Li, Danyang Wang, Ruigao Song, Chunwei Cao, Zhihua Zhang, Yu Wang, Xiaoli Li, Jiaojiao Huang, Qiang Liu, Naipeng Hou, Bingxiang Xu, Xiao Li, Xiaomeng Gao, Yan Jia, Jianguo Zhao, Yanfang Wang
Format: Article
Language:English
Published: BMC 2020-08-01
Series:Genome Biology
Subjects:
Pig
Online Access:http://link.springer.com/article/10.1186/s13059-020-02095-z
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language English
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author Feifei Li
Danyang Wang
Ruigao Song
Chunwei Cao
Zhihua Zhang
Yu Wang
Xiaoli Li
Jiaojiao Huang
Qiang Liu
Naipeng Hou
Bingxiang Xu
Xiao Li
Xiaomeng Gao
Yan Jia
Jianguo Zhao
Yanfang Wang
spellingShingle Feifei Li
Danyang Wang
Ruigao Song
Chunwei Cao
Zhihua Zhang
Yu Wang
Xiaoli Li
Jiaojiao Huang
Qiang Liu
Naipeng Hou
Bingxiang Xu
Xiao Li
Xiaomeng Gao
Yan Jia
Jianguo Zhao
Yanfang Wang
The asynchronous establishment of chromatin 3D architecture between in vitro fertilized and uniparental preimplantation pig embryos
Genome Biology
Pig
Early embryos
Chromatin 3D architecture
In vitro fertilization
Parthenogenesis
Androgenesis
author_facet Feifei Li
Danyang Wang
Ruigao Song
Chunwei Cao
Zhihua Zhang
Yu Wang
Xiaoli Li
Jiaojiao Huang
Qiang Liu
Naipeng Hou
Bingxiang Xu
Xiao Li
Xiaomeng Gao
Yan Jia
Jianguo Zhao
Yanfang Wang
author_sort Feifei Li
title The asynchronous establishment of chromatin 3D architecture between in vitro fertilized and uniparental preimplantation pig embryos
title_short The asynchronous establishment of chromatin 3D architecture between in vitro fertilized and uniparental preimplantation pig embryos
title_full The asynchronous establishment of chromatin 3D architecture between in vitro fertilized and uniparental preimplantation pig embryos
title_fullStr The asynchronous establishment of chromatin 3D architecture between in vitro fertilized and uniparental preimplantation pig embryos
title_full_unstemmed The asynchronous establishment of chromatin 3D architecture between in vitro fertilized and uniparental preimplantation pig embryos
title_sort asynchronous establishment of chromatin 3d architecture between in vitro fertilized and uniparental preimplantation pig embryos
publisher BMC
series Genome Biology
issn 1474-760X
publishDate 2020-08-01
description Abstract Background Pigs are important animals for agricultural and biomedical research, and improvement is needed for use of the assisted reproductive technologies. Determining underlying mechanisms of epigenetic reprogramming in the early stage of preimplantation embryos derived from in vitro fertilization (IVF), parthenogenesis, and androgenesis will not only contribute to assisted reproductive technologies of pigs but also will shed light into early human development. However, the reprogramming of three-dimensional architecture of chromatin in this process in pigs is poorly understood. Results We generate three-dimensional chromatin profiles for pig somatic cells, IVF, parthenogenesis, and androgenesis preimplantation embryos. We find that the chromosomes in the pig preimplantation embryos are enriched for superdomains, which are more rare in mice. However, p(s) curves, compartments, and topologically associated domains (TADs) are largely conserved in somatic cells and are gradually established during preimplantation embryogenesis in both mammals. In the uniparental pig embryos, the establishment of chromatin architecture is highly asynchronized at all levels from IVF embryos, and a remarkably strong decompartmentalization is observed during zygotic genome activation (ZGA). Finally, chromosomes originating from oocytes always establish TADs faster than chromosomes originating from sperm, both before and during ZGA. Conclusions Our data highlight a potential unique 3D chromatin pattern of enriched superdomains in pig preimplantation embryos, an unusual decompartmentalization process during ZGA in the uniparental embryos, and an asynchronized TAD reprogramming between maternal and paternal genomes, implying a severe dysregulation of ZGA in the uniparental embryos in pigs.
topic Pig
Early embryos
Chromatin 3D architecture
In vitro fertilization
Parthenogenesis
Androgenesis
url http://link.springer.com/article/10.1186/s13059-020-02095-z
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spelling doaj-5025e0547df244ba92888983ebad2ef62020-11-25T03:46:13ZengBMCGenome Biology1474-760X2020-08-0121112110.1186/s13059-020-02095-zThe asynchronous establishment of chromatin 3D architecture between in vitro fertilized and uniparental preimplantation pig embryosFeifei Li0Danyang Wang1Ruigao Song2Chunwei Cao3Zhihua Zhang4Yu Wang5Xiaoli Li6Jiaojiao Huang7Qiang Liu8Naipeng Hou9Bingxiang Xu10Xiao Li11Xiaomeng Gao12Yan Jia13Jianguo Zhao14Yanfang Wang15CAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, and China National Center for BioinformationCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, and China National Center for BioinformationUniversity of Chinese Academy of SciencesState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of SciencesCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, and China National Center for BioinformationState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of SciencesCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, and China National Center for BioinformationState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of SciencesState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of SciencesState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of SciencesCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, and China National Center for BioinformationCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, and China National Center for BioinformationCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, and China National Center for BioinformationCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, and China National Center for BioinformationUniversity of Chinese Academy of SciencesInstitute of Animal Science, Chinese Academy of Agricultural SciencesAbstract Background Pigs are important animals for agricultural and biomedical research, and improvement is needed for use of the assisted reproductive technologies. Determining underlying mechanisms of epigenetic reprogramming in the early stage of preimplantation embryos derived from in vitro fertilization (IVF), parthenogenesis, and androgenesis will not only contribute to assisted reproductive technologies of pigs but also will shed light into early human development. However, the reprogramming of three-dimensional architecture of chromatin in this process in pigs is poorly understood. Results We generate three-dimensional chromatin profiles for pig somatic cells, IVF, parthenogenesis, and androgenesis preimplantation embryos. We find that the chromosomes in the pig preimplantation embryos are enriched for superdomains, which are more rare in mice. However, p(s) curves, compartments, and topologically associated domains (TADs) are largely conserved in somatic cells and are gradually established during preimplantation embryogenesis in both mammals. In the uniparental pig embryos, the establishment of chromatin architecture is highly asynchronized at all levels from IVF embryos, and a remarkably strong decompartmentalization is observed during zygotic genome activation (ZGA). Finally, chromosomes originating from oocytes always establish TADs faster than chromosomes originating from sperm, both before and during ZGA. Conclusions Our data highlight a potential unique 3D chromatin pattern of enriched superdomains in pig preimplantation embryos, an unusual decompartmentalization process during ZGA in the uniparental embryos, and an asynchronized TAD reprogramming between maternal and paternal genomes, implying a severe dysregulation of ZGA in the uniparental embryos in pigs.http://link.springer.com/article/10.1186/s13059-020-02095-zPigEarly embryosChromatin 3D architectureIn vitro fertilizationParthenogenesisAndrogenesis