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Noncatalytic Function of a JmjC Domain Protein Disrupts Heterochromatin

Chromatin-modifying enzymes are frequently overexpressed in cancer cells, and their enzymatic activities play important roles in changing the epigenetic landscape responsible for tumorigenesis. However, many of these proteins also execute noncatalytic functions, which are poorly understood. In fissi...

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Detalles Bibliográficos
Autores principales: Bao, Kehan, Jia, Songtao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624913/
https://www.ncbi.nlm.nih.gov/pubmed/31321383
http://dx.doi.org/10.1177/2516865719862249
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author Bao, Kehan
Jia, Songtao
author_facet Bao, Kehan
Jia, Songtao
author_sort Bao, Kehan
collection PubMed
description Chromatin-modifying enzymes are frequently overexpressed in cancer cells, and their enzymatic activities play important roles in changing the epigenetic landscape responsible for tumorigenesis. However, many of these proteins also execute noncatalytic functions, which are poorly understood. In fission yeast, overexpression of Epe1, a histone demethylase homolog, causes heterochromatin defects. Interestingly, in our recent work, we discovered that overexpressed Epe1 recruits SAGA, a histone acetyltransferase complex important for transcriptional regulation, to disrupt heterochromatin, independent of its demethylase activity. Our findings suggest that overexpressed chromatin-modifying enzymes can alter the epigenetic landscape through changing their proteomic environments, an area that needs to be further explored in dissecting disease etiology associated with overexpression of chromatin regulators.
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spelling pubmed-66249132019-07-18 Noncatalytic Function of a JmjC Domain Protein Disrupts Heterochromatin Bao, Kehan Jia, Songtao Epigenet Insights Commentary Chromatin-modifying enzymes are frequently overexpressed in cancer cells, and their enzymatic activities play important roles in changing the epigenetic landscape responsible for tumorigenesis. However, many of these proteins also execute noncatalytic functions, which are poorly understood. In fission yeast, overexpression of Epe1, a histone demethylase homolog, causes heterochromatin defects. Interestingly, in our recent work, we discovered that overexpressed Epe1 recruits SAGA, a histone acetyltransferase complex important for transcriptional regulation, to disrupt heterochromatin, independent of its demethylase activity. Our findings suggest that overexpressed chromatin-modifying enzymes can alter the epigenetic landscape through changing their proteomic environments, an area that needs to be further explored in dissecting disease etiology associated with overexpression of chromatin regulators. SAGE Publications 2019-07-11 /pmc/articles/PMC6624913/ /pubmed/31321383 http://dx.doi.org/10.1177/2516865719862249 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Commentary
Bao, Kehan
Jia, Songtao
Noncatalytic Function of a JmjC Domain Protein Disrupts Heterochromatin
title Noncatalytic Function of a JmjC Domain Protein Disrupts Heterochromatin
title_full Noncatalytic Function of a JmjC Domain Protein Disrupts Heterochromatin
title_fullStr Noncatalytic Function of a JmjC Domain Protein Disrupts Heterochromatin
title_full_unstemmed Noncatalytic Function of a JmjC Domain Protein Disrupts Heterochromatin
title_short Noncatalytic Function of a JmjC Domain Protein Disrupts Heterochromatin
title_sort noncatalytic function of a jmjc domain protein disrupts heterochromatin
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624913/
https://www.ncbi.nlm.nih.gov/pubmed/31321383
http://dx.doi.org/10.1177/2516865719862249
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