Cargando…

Drosophila CTCF tandemly aligns with other insulator proteins at the borders of H3K27me3 domains

Several multiprotein DNA complexes capable of insulator activity have been identified in Drosophila melanogaster, yet only CTCF, a highly conserved zinc finger protein, and the transcription factor TFIIIC have been shown to function in mammals. CTCF is involved in diverse nuclear activities, and rec...

Descripción completa

Detalles Bibliográficos
Autores principales: Van Bortle, Kevin, Ramos, Edward, Takenaka, Naomi, Yang, Jingping, Wahi, Jessica E., Corces, Victor G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483547/
https://www.ncbi.nlm.nih.gov/pubmed/22722341
http://dx.doi.org/10.1101/gr.136788.111
_version_ 1782248016736944128
author Van Bortle, Kevin
Ramos, Edward
Takenaka, Naomi
Yang, Jingping
Wahi, Jessica E.
Corces, Victor G.
author_facet Van Bortle, Kevin
Ramos, Edward
Takenaka, Naomi
Yang, Jingping
Wahi, Jessica E.
Corces, Victor G.
author_sort Van Bortle, Kevin
collection PubMed
description Several multiprotein DNA complexes capable of insulator activity have been identified in Drosophila melanogaster, yet only CTCF, a highly conserved zinc finger protein, and the transcription factor TFIIIC have been shown to function in mammals. CTCF is involved in diverse nuclear activities, and recent studies suggest that the proteins with which it associates and the DNA sequences that it targets may underlie these various roles. Here we show that the Drosophila homolog of CTCF (dCTCF) aligns in the genome with other Drosophila insulator proteins such as Suppressor of Hairy wing [SU(HW)] and Boundary Element Associated Factor of 32 kDa (BEAF-32) at the borders of H3K27me3 domains, which are also enriched for associated insulator proteins and additional cofactors. RNAi depletion of dCTCF and combinatorial knockdown of gene expression for other Drosophila insulator proteins leads to a reduction in H3K27me3 levels within repressed domains, suggesting that insulators are important for the maintenance of appropriate repressive chromatin structure in Polycomb (Pc) domains. These results shed new insights into the roles of insulators in chromatin domain organization and support recent models suggesting that insulators underlie interactions important for Pc-mediated repression. We reveal an important relationship between dCTCF and other Drosophila insulator proteins and speculate that vertebrate CTCF may also align with other nuclear proteins to accomplish similar functions.
format Online
Article
Text
id pubmed-3483547
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Cold Spring Harbor Laboratory Press
record_format MEDLINE/PubMed
spelling pubmed-34835472013-05-01 Drosophila CTCF tandemly aligns with other insulator proteins at the borders of H3K27me3 domains Van Bortle, Kevin Ramos, Edward Takenaka, Naomi Yang, Jingping Wahi, Jessica E. Corces, Victor G. Genome Res Research Several multiprotein DNA complexes capable of insulator activity have been identified in Drosophila melanogaster, yet only CTCF, a highly conserved zinc finger protein, and the transcription factor TFIIIC have been shown to function in mammals. CTCF is involved in diverse nuclear activities, and recent studies suggest that the proteins with which it associates and the DNA sequences that it targets may underlie these various roles. Here we show that the Drosophila homolog of CTCF (dCTCF) aligns in the genome with other Drosophila insulator proteins such as Suppressor of Hairy wing [SU(HW)] and Boundary Element Associated Factor of 32 kDa (BEAF-32) at the borders of H3K27me3 domains, which are also enriched for associated insulator proteins and additional cofactors. RNAi depletion of dCTCF and combinatorial knockdown of gene expression for other Drosophila insulator proteins leads to a reduction in H3K27me3 levels within repressed domains, suggesting that insulators are important for the maintenance of appropriate repressive chromatin structure in Polycomb (Pc) domains. These results shed new insights into the roles of insulators in chromatin domain organization and support recent models suggesting that insulators underlie interactions important for Pc-mediated repression. We reveal an important relationship between dCTCF and other Drosophila insulator proteins and speculate that vertebrate CTCF may also align with other nuclear proteins to accomplish similar functions. Cold Spring Harbor Laboratory Press 2012-11 /pmc/articles/PMC3483547/ /pubmed/22722341 http://dx.doi.org/10.1101/gr.136788.111 Text en © 2012, Published by Cold Spring Harbor Laboratory Press This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported License), as described at http://creativecommons.org/licenses/by-nc/3.0/.
spellingShingle Research
Van Bortle, Kevin
Ramos, Edward
Takenaka, Naomi
Yang, Jingping
Wahi, Jessica E.
Corces, Victor G.
Drosophila CTCF tandemly aligns with other insulator proteins at the borders of H3K27me3 domains
title Drosophila CTCF tandemly aligns with other insulator proteins at the borders of H3K27me3 domains
title_full Drosophila CTCF tandemly aligns with other insulator proteins at the borders of H3K27me3 domains
title_fullStr Drosophila CTCF tandemly aligns with other insulator proteins at the borders of H3K27me3 domains
title_full_unstemmed Drosophila CTCF tandemly aligns with other insulator proteins at the borders of H3K27me3 domains
title_short Drosophila CTCF tandemly aligns with other insulator proteins at the borders of H3K27me3 domains
title_sort drosophila ctcf tandemly aligns with other insulator proteins at the borders of h3k27me3 domains
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483547/
https://www.ncbi.nlm.nih.gov/pubmed/22722341
http://dx.doi.org/10.1101/gr.136788.111
work_keys_str_mv AT vanbortlekevin drosophilactcftandemlyalignswithotherinsulatorproteinsatthebordersofh3k27me3domains
AT ramosedward drosophilactcftandemlyalignswithotherinsulatorproteinsatthebordersofh3k27me3domains
AT takenakanaomi drosophilactcftandemlyalignswithotherinsulatorproteinsatthebordersofh3k27me3domains
AT yangjingping drosophilactcftandemlyalignswithotherinsulatorproteinsatthebordersofh3k27me3domains
AT wahijessicae drosophilactcftandemlyalignswithotherinsulatorproteinsatthebordersofh3k27me3domains
AT corcesvictorg drosophilactcftandemlyalignswithotherinsulatorproteinsatthebordersofh3k27me3domains