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Epigenetic regulation of axon and dendrite growth
Neuroregenerative therapies for central nervous system (CNS) injury, neurodegenerative disease, or stroke require axons of damaged neurons to grow and re-innervate their targets. However, mature mammalian CNS neurons do not regenerate their axons, limiting recovery in these diseases. Although neuron...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3290832/ https://www.ncbi.nlm.nih.gov/pubmed/22403528 http://dx.doi.org/10.3389/fnmol.2012.00024 |
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author | Trakhtenberg, Ephraim F. Goldberg, Jeffrey L. |
author_facet | Trakhtenberg, Ephraim F. Goldberg, Jeffrey L. |
author_sort | Trakhtenberg, Ephraim F. |
collection | PubMed |
description | Neuroregenerative therapies for central nervous system (CNS) injury, neurodegenerative disease, or stroke require axons of damaged neurons to grow and re-innervate their targets. However, mature mammalian CNS neurons do not regenerate their axons, limiting recovery in these diseases. Although neurons' intrinsic capacity for axon growth may depend in part on the panoply of expressed transcription factors, epigenetic factors such as the accessibility of DNA and organization of chromatin are required for downstream genes to be transcribed. Thus, a potential approach to overcoming regenerative failure focuses on the epigenetic mechanisms regulating regenerative gene expression in the CNS. Here we review molecular mechanisms regulating the epigenetic state of DNA through chromatin modifications, their implications for regulating axon and dendrite growth, and important new directions for this field of study. |
format | Online Article Text |
id | pubmed-3290832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-32908322012-03-08 Epigenetic regulation of axon and dendrite growth Trakhtenberg, Ephraim F. Goldberg, Jeffrey L. Front Mol Neurosci Neuroscience Neuroregenerative therapies for central nervous system (CNS) injury, neurodegenerative disease, or stroke require axons of damaged neurons to grow and re-innervate their targets. However, mature mammalian CNS neurons do not regenerate their axons, limiting recovery in these diseases. Although neurons' intrinsic capacity for axon growth may depend in part on the panoply of expressed transcription factors, epigenetic factors such as the accessibility of DNA and organization of chromatin are required for downstream genes to be transcribed. Thus, a potential approach to overcoming regenerative failure focuses on the epigenetic mechanisms regulating regenerative gene expression in the CNS. Here we review molecular mechanisms regulating the epigenetic state of DNA through chromatin modifications, their implications for regulating axon and dendrite growth, and important new directions for this field of study. Frontiers Media S.A. 2012-03-01 /pmc/articles/PMC3290832/ /pubmed/22403528 http://dx.doi.org/10.3389/fnmol.2012.00024 Text en Copyright © 2012 Trakhtenberg and Goldberg. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited. |
spellingShingle | Neuroscience Trakhtenberg, Ephraim F. Goldberg, Jeffrey L. Epigenetic regulation of axon and dendrite growth |
title | Epigenetic regulation of axon and dendrite growth |
title_full | Epigenetic regulation of axon and dendrite growth |
title_fullStr | Epigenetic regulation of axon and dendrite growth |
title_full_unstemmed | Epigenetic regulation of axon and dendrite growth |
title_short | Epigenetic regulation of axon and dendrite growth |
title_sort | epigenetic regulation of axon and dendrite growth |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3290832/ https://www.ncbi.nlm.nih.gov/pubmed/22403528 http://dx.doi.org/10.3389/fnmol.2012.00024 |
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