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How substrate specificity is imposed on a histone demethylase—lessons from KDM2A

Histone lysine methylation and demethylation regulate histone methylation dynamics, which impacts chromatin structure and function. To read and erase the methylated histone residues, lysine demethylases must specifically recognize the histone sequences and methylated sites and discriminate the degre...

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Detalles Bibliográficos
Autores principales: Tsai, Chi-Lin, Shi, Yang, Tainer, John A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197959/
https://www.ncbi.nlm.nih.gov/pubmed/25128493
http://dx.doi.org/10.1101/gad.249755.114
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author Tsai, Chi-Lin
Shi, Yang
Tainer, John A.
author_facet Tsai, Chi-Lin
Shi, Yang
Tainer, John A.
author_sort Tsai, Chi-Lin
collection PubMed
description Histone lysine methylation and demethylation regulate histone methylation dynamics, which impacts chromatin structure and function. To read and erase the methylated histone residues, lysine demethylases must specifically recognize the histone sequences and methylated sites and discriminate the degree of these methylations. In this issue of Genes & Development, Cheng and colleagues (pp. 1758–1771) determine a crystal structure of histone lysine demethylase KDM2A that specifically targets lower degrees of H3K36 methylation. The results reveal the structural basis for H3K36 substrate specificity and suggest mechanisms of Lys36 demethylation. This KDM2A–H3K36 complex structure, coupled with functional studies, provides needed insight into the process and regulation of histone demethylation.
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spelling pubmed-41979592015-02-15 How substrate specificity is imposed on a histone demethylase—lessons from KDM2A Tsai, Chi-Lin Shi, Yang Tainer, John A. Genes Dev Perspective Histone lysine methylation and demethylation regulate histone methylation dynamics, which impacts chromatin structure and function. To read and erase the methylated histone residues, lysine demethylases must specifically recognize the histone sequences and methylated sites and discriminate the degree of these methylations. In this issue of Genes & Development, Cheng and colleagues (pp. 1758–1771) determine a crystal structure of histone lysine demethylase KDM2A that specifically targets lower degrees of H3K36 methylation. The results reveal the structural basis for H3K36 substrate specificity and suggest mechanisms of Lys36 demethylation. This KDM2A–H3K36 complex structure, coupled with functional studies, provides needed insight into the process and regulation of histone demethylation. Cold Spring Harbor Laboratory Press 2014-08-15 /pmc/articles/PMC4197959/ /pubmed/25128493 http://dx.doi.org/10.1101/gad.249755.114 Text en © 2014 Tsai et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Perspective
Tsai, Chi-Lin
Shi, Yang
Tainer, John A.
How substrate specificity is imposed on a histone demethylase—lessons from KDM2A
title How substrate specificity is imposed on a histone demethylase—lessons from KDM2A
title_full How substrate specificity is imposed on a histone demethylase—lessons from KDM2A
title_fullStr How substrate specificity is imposed on a histone demethylase—lessons from KDM2A
title_full_unstemmed How substrate specificity is imposed on a histone demethylase—lessons from KDM2A
title_short How substrate specificity is imposed on a histone demethylase—lessons from KDM2A
title_sort how substrate specificity is imposed on a histone demethylase—lessons from kdm2a
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197959/
https://www.ncbi.nlm.nih.gov/pubmed/25128493
http://dx.doi.org/10.1101/gad.249755.114
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