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Correction of Heritable Epigenetic Defects Using Editing Tools

Epimutations refer to mistakes in the setting or maintenance of epigenetic marks in the chromatin. They lead to mis-expression of genes and are often secondary to germline transmitted mutations. As such, they are the cause for a considerable number of genetically inherited conditions in humans. The...

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Detalles Bibliográficos
Autores principales: Handal, Tayma, Eiges, Rachel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070094/
https://www.ncbi.nlm.nih.gov/pubmed/33921346
http://dx.doi.org/10.3390/ijms22083966
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author Handal, Tayma
Eiges, Rachel
author_facet Handal, Tayma
Eiges, Rachel
author_sort Handal, Tayma
collection PubMed
description Epimutations refer to mistakes in the setting or maintenance of epigenetic marks in the chromatin. They lead to mis-expression of genes and are often secondary to germline transmitted mutations. As such, they are the cause for a considerable number of genetically inherited conditions in humans. The correction of these types of epigenetic defects constitutes a good paradigm to probe the fundamental mechanisms underlying the development of these diseases, and the molecular basis for the establishment, maintenance and regulation of epigenetic modifications in general. Here, we review the data to date, which is limited to repetitive elements, that relates to the applications of key editing tools for addressing the epigenetic aspects of various epigenetically regulated diseases. For each approach we summarize the efforts conducted to date, highlight their contribution to a better understanding of the molecular basis of epigenetic mechanisms, describe the limitations of each approach and suggest perspectives for further exploration in this field.
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spelling pubmed-80700942021-04-26 Correction of Heritable Epigenetic Defects Using Editing Tools Handal, Tayma Eiges, Rachel Int J Mol Sci Review Epimutations refer to mistakes in the setting or maintenance of epigenetic marks in the chromatin. They lead to mis-expression of genes and are often secondary to germline transmitted mutations. As such, they are the cause for a considerable number of genetically inherited conditions in humans. The correction of these types of epigenetic defects constitutes a good paradigm to probe the fundamental mechanisms underlying the development of these diseases, and the molecular basis for the establishment, maintenance and regulation of epigenetic modifications in general. Here, we review the data to date, which is limited to repetitive elements, that relates to the applications of key editing tools for addressing the epigenetic aspects of various epigenetically regulated diseases. For each approach we summarize the efforts conducted to date, highlight their contribution to a better understanding of the molecular basis of epigenetic mechanisms, describe the limitations of each approach and suggest perspectives for further exploration in this field. MDPI 2021-04-12 /pmc/articles/PMC8070094/ /pubmed/33921346 http://dx.doi.org/10.3390/ijms22083966 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Handal, Tayma
Eiges, Rachel
Correction of Heritable Epigenetic Defects Using Editing Tools
title Correction of Heritable Epigenetic Defects Using Editing Tools
title_full Correction of Heritable Epigenetic Defects Using Editing Tools
title_fullStr Correction of Heritable Epigenetic Defects Using Editing Tools
title_full_unstemmed Correction of Heritable Epigenetic Defects Using Editing Tools
title_short Correction of Heritable Epigenetic Defects Using Editing Tools
title_sort correction of heritable epigenetic defects using editing tools
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070094/
https://www.ncbi.nlm.nih.gov/pubmed/33921346
http://dx.doi.org/10.3390/ijms22083966
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