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CTCF regulates the local epigenetic state of ribosomal DNA repeats

BACKGROUND: CCCTC binding factor (CTCF) is a highly conserved zinc finger protein, which is involved in chromatin organization, local histone modifications, and RNA polymerase II-mediated gene transcription. CTCF may act by binding tightly to DNA and recruiting other proteins to mediate its various...

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Autores principales: van de Nobelen, Suzanne, Rosa-Garrido, Manuel, Leers, Joerg, Heath, Helen, Soochit, Widia, Joosen, Linda, Jonkers, Iris, Demmers, Jeroen, van der Reijden, Michael, Torrano, Verónica, Grosveld, Frank, Delgado, M Dolores, Renkawitz, Rainer, Galjart, Niels, Sleutels, Frank
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993708/
https://www.ncbi.nlm.nih.gov/pubmed/21059229
http://dx.doi.org/10.1186/1756-8935-3-19
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author van de Nobelen, Suzanne
Rosa-Garrido, Manuel
Leers, Joerg
Heath, Helen
Soochit, Widia
Joosen, Linda
Jonkers, Iris
Demmers, Jeroen
van der Reijden, Michael
Torrano, Verónica
Grosveld, Frank
Delgado, M Dolores
Renkawitz, Rainer
Galjart, Niels
Sleutels, Frank
author_facet van de Nobelen, Suzanne
Rosa-Garrido, Manuel
Leers, Joerg
Heath, Helen
Soochit, Widia
Joosen, Linda
Jonkers, Iris
Demmers, Jeroen
van der Reijden, Michael
Torrano, Verónica
Grosveld, Frank
Delgado, M Dolores
Renkawitz, Rainer
Galjart, Niels
Sleutels, Frank
author_sort van de Nobelen, Suzanne
collection PubMed
description BACKGROUND: CCCTC binding factor (CTCF) is a highly conserved zinc finger protein, which is involved in chromatin organization, local histone modifications, and RNA polymerase II-mediated gene transcription. CTCF may act by binding tightly to DNA and recruiting other proteins to mediate its various functions in the nucleus. To further explore the role of this essential factor, we used a mass spectrometry-based approach to screen for novel CTCF-interacting partners. RESULTS: Using biotinylated CTCF as bait, we identified upstream binding factor (UBF) and multiple other components of the RNA polymerase I complex as potential CTCF-interacting partners. Interestingly, CTCFL, the testis-specific paralog of CTCF, also binds UBF. The interaction between CTCF(L) and UBF is direct, and requires the zinc finger domain of CTCF(L) and the high mobility group (HMG)-box 1 and dimerization domain of UBF. Because UBF is involved in RNA polymerase I-mediated ribosomal (r)RNA transcription, we analyzed CTCF binding to the rDNA repeat. We found that CTCF bound to a site upstream of the rDNA spacer promoter and preferred non-methylated over methylated rDNA. DNA binding by CTCF in turn stimulated binding of UBF. Absence of CTCF in cultured cells resulted in decreased association of UBF with rDNA and in nucleolar fusion. Furthermore, lack of CTCF led to reduced binding of RNA polymerase I and variant histone H2A.Z near the rDNA spacer promoter, a loss of specific histone modifications, and diminished transcription of non-coding RNA from the spacer promoter. CONCLUSIONS: UBF is the first common interaction partner of CTCF and CTCFL, suggesting a role for these proteins in chromatin organization of the rDNA repeats. We propose that CTCF affects RNA polymerase I-mediated events globally by controlling nucleolar number, and locally by regulating chromatin at the rDNA spacer promoter, similar to RNA polymerase II promoters. CTCF may load UBF onto rDNA, thereby forming part of a network that maintains rDNA genes poised for transcription.
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spelling pubmed-29937082010-11-30 CTCF regulates the local epigenetic state of ribosomal DNA repeats van de Nobelen, Suzanne Rosa-Garrido, Manuel Leers, Joerg Heath, Helen Soochit, Widia Joosen, Linda Jonkers, Iris Demmers, Jeroen van der Reijden, Michael Torrano, Verónica Grosveld, Frank Delgado, M Dolores Renkawitz, Rainer Galjart, Niels Sleutels, Frank Epigenetics Chromatin Research BACKGROUND: CCCTC binding factor (CTCF) is a highly conserved zinc finger protein, which is involved in chromatin organization, local histone modifications, and RNA polymerase II-mediated gene transcription. CTCF may act by binding tightly to DNA and recruiting other proteins to mediate its various functions in the nucleus. To further explore the role of this essential factor, we used a mass spectrometry-based approach to screen for novel CTCF-interacting partners. RESULTS: Using biotinylated CTCF as bait, we identified upstream binding factor (UBF) and multiple other components of the RNA polymerase I complex as potential CTCF-interacting partners. Interestingly, CTCFL, the testis-specific paralog of CTCF, also binds UBF. The interaction between CTCF(L) and UBF is direct, and requires the zinc finger domain of CTCF(L) and the high mobility group (HMG)-box 1 and dimerization domain of UBF. Because UBF is involved in RNA polymerase I-mediated ribosomal (r)RNA transcription, we analyzed CTCF binding to the rDNA repeat. We found that CTCF bound to a site upstream of the rDNA spacer promoter and preferred non-methylated over methylated rDNA. DNA binding by CTCF in turn stimulated binding of UBF. Absence of CTCF in cultured cells resulted in decreased association of UBF with rDNA and in nucleolar fusion. Furthermore, lack of CTCF led to reduced binding of RNA polymerase I and variant histone H2A.Z near the rDNA spacer promoter, a loss of specific histone modifications, and diminished transcription of non-coding RNA from the spacer promoter. CONCLUSIONS: UBF is the first common interaction partner of CTCF and CTCFL, suggesting a role for these proteins in chromatin organization of the rDNA repeats. We propose that CTCF affects RNA polymerase I-mediated events globally by controlling nucleolar number, and locally by regulating chromatin at the rDNA spacer promoter, similar to RNA polymerase II promoters. CTCF may load UBF onto rDNA, thereby forming part of a network that maintains rDNA genes poised for transcription. BioMed Central 2010-11-08 /pmc/articles/PMC2993708/ /pubmed/21059229 http://dx.doi.org/10.1186/1756-8935-3-19 Text en Copyright ©2010 van de Nobelen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
van de Nobelen, Suzanne
Rosa-Garrido, Manuel
Leers, Joerg
Heath, Helen
Soochit, Widia
Joosen, Linda
Jonkers, Iris
Demmers, Jeroen
van der Reijden, Michael
Torrano, Verónica
Grosveld, Frank
Delgado, M Dolores
Renkawitz, Rainer
Galjart, Niels
Sleutels, Frank
CTCF regulates the local epigenetic state of ribosomal DNA repeats
title CTCF regulates the local epigenetic state of ribosomal DNA repeats
title_full CTCF regulates the local epigenetic state of ribosomal DNA repeats
title_fullStr CTCF regulates the local epigenetic state of ribosomal DNA repeats
title_full_unstemmed CTCF regulates the local epigenetic state of ribosomal DNA repeats
title_short CTCF regulates the local epigenetic state of ribosomal DNA repeats
title_sort ctcf regulates the local epigenetic state of ribosomal dna repeats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993708/
https://www.ncbi.nlm.nih.gov/pubmed/21059229
http://dx.doi.org/10.1186/1756-8935-3-19
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