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Handpicking epigenetic marks with PHD fingers

Plant homeodomain (PHD) fingers have emerged as one of the largest families of epigenetic effectors capable of recognizing or ‘reading’ post-translational histone modifications and unmodified histone tails. These interactions are highly specific and can be modulated by the neighboring epigenetic mar...

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Detalles Bibliográficos
Autores principales: Musselman, Catherine A., Kutateladze, Tatiana G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3241642/
https://www.ncbi.nlm.nih.gov/pubmed/21813457
http://dx.doi.org/10.1093/nar/gkr613
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author Musselman, Catherine A.
Kutateladze, Tatiana G.
author_facet Musselman, Catherine A.
Kutateladze, Tatiana G.
author_sort Musselman, Catherine A.
collection PubMed
description Plant homeodomain (PHD) fingers have emerged as one of the largest families of epigenetic effectors capable of recognizing or ‘reading’ post-translational histone modifications and unmodified histone tails. These interactions are highly specific and can be modulated by the neighboring epigenetic marks and adjacent effectors. A few PHD fingers have recently been found to also associate with non-histone proteins. In this review, we detail the molecular mechanisms and biological outcomes of the histone and non-histone targeting by PHD fingers. We discuss the significance of crosstalk between the histone modifications and consequences of combinatorial readout for selective recruitment of the PHD finger-containing components of chromatin remodeling and transcriptional complexes.
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spelling pubmed-32416422011-12-19 Handpicking epigenetic marks with PHD fingers Musselman, Catherine A. Kutateladze, Tatiana G. Nucleic Acids Res Survey and Summary Plant homeodomain (PHD) fingers have emerged as one of the largest families of epigenetic effectors capable of recognizing or ‘reading’ post-translational histone modifications and unmodified histone tails. These interactions are highly specific and can be modulated by the neighboring epigenetic marks and adjacent effectors. A few PHD fingers have recently been found to also associate with non-histone proteins. In this review, we detail the molecular mechanisms and biological outcomes of the histone and non-histone targeting by PHD fingers. We discuss the significance of crosstalk between the histone modifications and consequences of combinatorial readout for selective recruitment of the PHD finger-containing components of chromatin remodeling and transcriptional complexes. Oxford University Press 2011-11 2011-08-03 /pmc/articles/PMC3241642/ /pubmed/21813457 http://dx.doi.org/10.1093/nar/gkr613 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Survey and Summary
Musselman, Catherine A.
Kutateladze, Tatiana G.
Handpicking epigenetic marks with PHD fingers
title Handpicking epigenetic marks with PHD fingers
title_full Handpicking epigenetic marks with PHD fingers
title_fullStr Handpicking epigenetic marks with PHD fingers
title_full_unstemmed Handpicking epigenetic marks with PHD fingers
title_short Handpicking epigenetic marks with PHD fingers
title_sort handpicking epigenetic marks with phd fingers
topic Survey and Summary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3241642/
https://www.ncbi.nlm.nih.gov/pubmed/21813457
http://dx.doi.org/10.1093/nar/gkr613
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