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Hansel, Gretel, and the Consequences of Failing to Remove Histone Methylation Breadcrumbs

Like breadcrumbs in the forest, cotranscriptionally acquired histone methylation acts as a memory of prior transcription. Because it can be retained through cell divisions, transcriptional memory allows cells to coordinate complex transcriptional programs during development. However, if not reprogra...

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Detalles Bibliográficos
Autores principales: Lee, Teresa W., Katz, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10047806/
https://www.ncbi.nlm.nih.gov/pubmed/32007289
http://dx.doi.org/10.1016/j.tig.2019.12.004
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author Lee, Teresa W.
Katz, David J.
author_facet Lee, Teresa W.
Katz, David J.
author_sort Lee, Teresa W.
collection PubMed
description Like breadcrumbs in the forest, cotranscriptionally acquired histone methylation acts as a memory of prior transcription. Because it can be retained through cell divisions, transcriptional memory allows cells to coordinate complex transcriptional programs during development. However, if not reprogrammed properly during cell fate transitions, it can also disrupt cellular identity. In this review, we discuss the consequences of failure to reprogram histone methylation during three crucial epigenetic reprogramming windows: maternal reprogramming at fertilization, embryonic stem cell (ESC) differentiation, and the continuous maintenance of cell identity in differentiated cells. In addition, we discuss how following the wrong breadcrumb trail of transcriptional memory provides a framework for understanding how heterozygous loss-of-function mutations in histone-modifying enzymes may cause severe neurodevelopmental disorders.
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spelling pubmed-100478062023-03-28 Hansel, Gretel, and the Consequences of Failing to Remove Histone Methylation Breadcrumbs Lee, Teresa W. Katz, David J. Trends Genet Article Like breadcrumbs in the forest, cotranscriptionally acquired histone methylation acts as a memory of prior transcription. Because it can be retained through cell divisions, transcriptional memory allows cells to coordinate complex transcriptional programs during development. However, if not reprogrammed properly during cell fate transitions, it can also disrupt cellular identity. In this review, we discuss the consequences of failure to reprogram histone methylation during three crucial epigenetic reprogramming windows: maternal reprogramming at fertilization, embryonic stem cell (ESC) differentiation, and the continuous maintenance of cell identity in differentiated cells. In addition, we discuss how following the wrong breadcrumb trail of transcriptional memory provides a framework for understanding how heterozygous loss-of-function mutations in histone-modifying enzymes may cause severe neurodevelopmental disorders. 2020-03 2020-01-29 /pmc/articles/PMC10047806/ /pubmed/32007289 http://dx.doi.org/10.1016/j.tig.2019.12.004 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Lee, Teresa W.
Katz, David J.
Hansel, Gretel, and the Consequences of Failing to Remove Histone Methylation Breadcrumbs
title Hansel, Gretel, and the Consequences of Failing to Remove Histone Methylation Breadcrumbs
title_full Hansel, Gretel, and the Consequences of Failing to Remove Histone Methylation Breadcrumbs
title_fullStr Hansel, Gretel, and the Consequences of Failing to Remove Histone Methylation Breadcrumbs
title_full_unstemmed Hansel, Gretel, and the Consequences of Failing to Remove Histone Methylation Breadcrumbs
title_short Hansel, Gretel, and the Consequences of Failing to Remove Histone Methylation Breadcrumbs
title_sort hansel, gretel, and the consequences of failing to remove histone methylation breadcrumbs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10047806/
https://www.ncbi.nlm.nih.gov/pubmed/32007289
http://dx.doi.org/10.1016/j.tig.2019.12.004
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