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Sequential chromatin immunoprecipitation to detect SUMOylated MeCP2 in neurons

The small ubiquitin-like modifier (SUMO) is a short peptide that can be covalently linked to proteins altering their function. SUMOylation is an essential post-translational modification (PTM). Because of its dynamic nature, low abundance levels, and technical limitations, the occupation of endogeno...

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Detalles Bibliográficos
Autores principales: Wu, Tao, Donohoe, Mary E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600420/
https://www.ncbi.nlm.nih.gov/pubmed/28944302
http://dx.doi.org/10.1016/j.bbrep.2016.01.014
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author Wu, Tao
Donohoe, Mary E.
author_facet Wu, Tao
Donohoe, Mary E.
author_sort Wu, Tao
collection PubMed
description The small ubiquitin-like modifier (SUMO) is a short peptide that can be covalently linked to proteins altering their function. SUMOylation is an essential post-translational modification (PTM). Because of its dynamic nature, low abundance levels, and technical limitations, the occupation of endogenous SUMOylated transcription factors at genomic loci is challenging to detect. The chromatin regulator Methyl CpG binding protein 2 (MeCP2) is subjected to PTMs including SUMO. Mutations in MeCP2 lead to Rett syndrome, a severe neurodevelopmental disorder. Here, we present an efficient method to perform sequential chromatin immunoprecipitation (Seq-ChIP) for detecting SUMOylated MeCP2 in neurons. This Seq-ChIP technique is a useful tool to determine the occupancy of SUMOylated transcription and chromatin factors at specific genomic regions.
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spelling pubmed-56004202017-09-20 Sequential chromatin immunoprecipitation to detect SUMOylated MeCP2 in neurons Wu, Tao Donohoe, Mary E. Biochem Biophys Rep Research Article The small ubiquitin-like modifier (SUMO) is a short peptide that can be covalently linked to proteins altering their function. SUMOylation is an essential post-translational modification (PTM). Because of its dynamic nature, low abundance levels, and technical limitations, the occupation of endogenous SUMOylated transcription factors at genomic loci is challenging to detect. The chromatin regulator Methyl CpG binding protein 2 (MeCP2) is subjected to PTMs including SUMO. Mutations in MeCP2 lead to Rett syndrome, a severe neurodevelopmental disorder. Here, we present an efficient method to perform sequential chromatin immunoprecipitation (Seq-ChIP) for detecting SUMOylated MeCP2 in neurons. This Seq-ChIP technique is a useful tool to determine the occupancy of SUMOylated transcription and chromatin factors at specific genomic regions. Elsevier 2016-01-23 /pmc/articles/PMC5600420/ /pubmed/28944302 http://dx.doi.org/10.1016/j.bbrep.2016.01.014 Text en © 2016 Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Wu, Tao
Donohoe, Mary E.
Sequential chromatin immunoprecipitation to detect SUMOylated MeCP2 in neurons
title Sequential chromatin immunoprecipitation to detect SUMOylated MeCP2 in neurons
title_full Sequential chromatin immunoprecipitation to detect SUMOylated MeCP2 in neurons
title_fullStr Sequential chromatin immunoprecipitation to detect SUMOylated MeCP2 in neurons
title_full_unstemmed Sequential chromatin immunoprecipitation to detect SUMOylated MeCP2 in neurons
title_short Sequential chromatin immunoprecipitation to detect SUMOylated MeCP2 in neurons
title_sort sequential chromatin immunoprecipitation to detect sumoylated mecp2 in neurons
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600420/
https://www.ncbi.nlm.nih.gov/pubmed/28944302
http://dx.doi.org/10.1016/j.bbrep.2016.01.014
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