Cargando…
Successful generation of epigenetic disease model mice by targeted demethylation of the epigenome
BACKGROUND: Epigenetic modifications, including DNA methylation, play an important role in gene silencing and genome stability. Consequently, epigenetic dysregulation can cause several diseases, such as cancer, obesity, diabetes, autism, and imprinting disorders. RESULTS: We validate three methods f...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7110793/ https://www.ncbi.nlm.nih.gov/pubmed/32234052 http://dx.doi.org/10.1186/s13059-020-01991-8 |
_version_ | 1783513137384783872 |
---|---|
author | Horii, Takuro Morita, Sumiyo Hino, Shinjiro Kimura, Mika Hino, Yuko Kogo, Hiroshi Nakao, Mitsuyoshi Hatada, Izuho |
author_facet | Horii, Takuro Morita, Sumiyo Hino, Shinjiro Kimura, Mika Hino, Yuko Kogo, Hiroshi Nakao, Mitsuyoshi Hatada, Izuho |
author_sort | Horii, Takuro |
collection | PubMed |
description | BACKGROUND: Epigenetic modifications, including DNA methylation, play an important role in gene silencing and genome stability. Consequently, epigenetic dysregulation can cause several diseases, such as cancer, obesity, diabetes, autism, and imprinting disorders. RESULTS: We validate three methods for the generation of epigenome-edited mice using the dCas9-SunTag and single-chain variable fragment-TET1 catalytic domain. We generate model mice for Silver-Russell syndrome (SRS), an imprinting disorder, by target-specific DNA demethylation in the H19 differentially methylated region. Like SRS patients, these mice show H19 upregulation and Igf2 downregulation, leading to severe intrauterine and postnatal growth retardation. CONCLUSION: This is the first report of an imprinting disease model animal generated by targeted demethylation of specific loci of the epigenome in fertilized eggs. Epigenome-edited animals are also useful for exploring the causative epimutations in epigenetic diseases. |
format | Online Article Text |
id | pubmed-7110793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71107932020-04-07 Successful generation of epigenetic disease model mice by targeted demethylation of the epigenome Horii, Takuro Morita, Sumiyo Hino, Shinjiro Kimura, Mika Hino, Yuko Kogo, Hiroshi Nakao, Mitsuyoshi Hatada, Izuho Genome Biol Research BACKGROUND: Epigenetic modifications, including DNA methylation, play an important role in gene silencing and genome stability. Consequently, epigenetic dysregulation can cause several diseases, such as cancer, obesity, diabetes, autism, and imprinting disorders. RESULTS: We validate three methods for the generation of epigenome-edited mice using the dCas9-SunTag and single-chain variable fragment-TET1 catalytic domain. We generate model mice for Silver-Russell syndrome (SRS), an imprinting disorder, by target-specific DNA demethylation in the H19 differentially methylated region. Like SRS patients, these mice show H19 upregulation and Igf2 downregulation, leading to severe intrauterine and postnatal growth retardation. CONCLUSION: This is the first report of an imprinting disease model animal generated by targeted demethylation of specific loci of the epigenome in fertilized eggs. Epigenome-edited animals are also useful for exploring the causative epimutations in epigenetic diseases. BioMed Central 2020-04-01 /pmc/articles/PMC7110793/ /pubmed/32234052 http://dx.doi.org/10.1186/s13059-020-01991-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Horii, Takuro Morita, Sumiyo Hino, Shinjiro Kimura, Mika Hino, Yuko Kogo, Hiroshi Nakao, Mitsuyoshi Hatada, Izuho Successful generation of epigenetic disease model mice by targeted demethylation of the epigenome |
title | Successful generation of epigenetic disease model mice by targeted demethylation of the epigenome |
title_full | Successful generation of epigenetic disease model mice by targeted demethylation of the epigenome |
title_fullStr | Successful generation of epigenetic disease model mice by targeted demethylation of the epigenome |
title_full_unstemmed | Successful generation of epigenetic disease model mice by targeted demethylation of the epigenome |
title_short | Successful generation of epigenetic disease model mice by targeted demethylation of the epigenome |
title_sort | successful generation of epigenetic disease model mice by targeted demethylation of the epigenome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7110793/ https://www.ncbi.nlm.nih.gov/pubmed/32234052 http://dx.doi.org/10.1186/s13059-020-01991-8 |
work_keys_str_mv | AT horiitakuro successfulgenerationofepigeneticdiseasemodelmicebytargeteddemethylationoftheepigenome AT moritasumiyo successfulgenerationofepigeneticdiseasemodelmicebytargeteddemethylationoftheepigenome AT hinoshinjiro successfulgenerationofepigeneticdiseasemodelmicebytargeteddemethylationoftheepigenome AT kimuramika successfulgenerationofepigeneticdiseasemodelmicebytargeteddemethylationoftheepigenome AT hinoyuko successfulgenerationofepigeneticdiseasemodelmicebytargeteddemethylationoftheepigenome AT kogohiroshi successfulgenerationofepigeneticdiseasemodelmicebytargeteddemethylationoftheepigenome AT nakaomitsuyoshi successfulgenerationofepigeneticdiseasemodelmicebytargeteddemethylationoftheepigenome AT hatadaizuho successfulgenerationofepigeneticdiseasemodelmicebytargeteddemethylationoftheepigenome |