A possible role of Drosophila CTCF in mitotic bookmarking and maintaining chromatin domains during the cell cycle

BACKGROUND: The CCCTC-binding factor (CTCF) is a highly conserved insulator protein that plays various roles in many cellular processes. CTCF is one of the main architecture proteins in higher eukaryotes, and in combination with other architecture proteins and regulators, also shapes the three-dimensional organization of a genome. Experiments show CTCF partially remains associated with chromatin during mitosis. However, the role of CTCF in the maintenance and propagation of genome architectures throughout the cell cycle remains elusive. RESULTS: We performed a comprehensive bioinformatics analysis on public datasets of Drosophila CTCF (dCTCF). We characterized dCTCF-binding sites according to their occupancy status during the cell cycle, and identified three classes: interphase-mitosis-common (IM), interphase-only (IO) and mitosis-only (MO) sites. Integrated function analysis showed dCTCF-binding sites of different classes might be involved in different biological processes, and IM sites were more conserved and more intensely bound. dCTCF-binding sites of the same class preferentially localized closer to each other, and were highly enriched at chromatin syntenic and topologically associating domains boundaries. CONCLUSIONS: Our results revealed different functions of dCTCF during the cell cycle and suggested that dCTCF might contribute to the establishment of the three-dimensional architecture of the Drosophila genome by maintaining local chromatin compartments throughout the whole cell cycle.

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Main Authors: Shen,Wenlong, Wang,Dong, Ye,Bingyu, Shi,Minglei, Zhang,Yan, Zhao,Zhihu
Format: Digital revista
Language:English
Published: Sociedad de Biología de Chile 2015
Online Access:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602015000100027
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spelling oai:scielo:S0716-976020150001000272016-02-16A possible role of Drosophila CTCF in mitotic bookmarking and maintaining chromatin domains during the cell cycleShen,WenlongWang,DongYe,BingyuShi,MingleiZhang,YanZhao,Zhihu dCTCF Cell cycle Chromatin domains Mitotic bookmarking Bioinformatics BACKGROUND: The CCCTC-binding factor (CTCF) is a highly conserved insulator protein that plays various roles in many cellular processes. CTCF is one of the main architecture proteins in higher eukaryotes, and in combination with other architecture proteins and regulators, also shapes the three-dimensional organization of a genome. Experiments show CTCF partially remains associated with chromatin during mitosis. However, the role of CTCF in the maintenance and propagation of genome architectures throughout the cell cycle remains elusive. RESULTS: We performed a comprehensive bioinformatics analysis on public datasets of Drosophila CTCF (dCTCF). We characterized dCTCF-binding sites according to their occupancy status during the cell cycle, and identified three classes: interphase-mitosis-common (IM), interphase-only (IO) and mitosis-only (MO) sites. Integrated function analysis showed dCTCF-binding sites of different classes might be involved in different biological processes, and IM sites were more conserved and more intensely bound. dCTCF-binding sites of the same class preferentially localized closer to each other, and were highly enriched at chromatin syntenic and topologically associating domains boundaries. CONCLUSIONS: Our results revealed different functions of dCTCF during the cell cycle and suggested that dCTCF might contribute to the establishment of the three-dimensional architecture of the Drosophila genome by maintaining local chromatin compartments throughout the whole cell cycle.info:eu-repo/semantics/openAccessSociedad de Biología de ChileBiological Research v.48 20152015-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602015000100027en10.1186/S40659-015-0019-6
institution SCIELO
collection OJS
country Chile
countrycode CL
component Revista
access En linea
databasecode rev-scielo-cl
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Shen,Wenlong
Wang,Dong
Ye,Bingyu
Shi,Minglei
Zhang,Yan
Zhao,Zhihu
spellingShingle Shen,Wenlong
Wang,Dong
Ye,Bingyu
Shi,Minglei
Zhang,Yan
Zhao,Zhihu
A possible role of Drosophila CTCF in mitotic bookmarking and maintaining chromatin domains during the cell cycle
author_facet Shen,Wenlong
Wang,Dong
Ye,Bingyu
Shi,Minglei
Zhang,Yan
Zhao,Zhihu
author_sort Shen,Wenlong
title A possible role of Drosophila CTCF in mitotic bookmarking and maintaining chromatin domains during the cell cycle
title_short A possible role of Drosophila CTCF in mitotic bookmarking and maintaining chromatin domains during the cell cycle
title_full A possible role of Drosophila CTCF in mitotic bookmarking and maintaining chromatin domains during the cell cycle
title_fullStr A possible role of Drosophila CTCF in mitotic bookmarking and maintaining chromatin domains during the cell cycle
title_full_unstemmed A possible role of Drosophila CTCF in mitotic bookmarking and maintaining chromatin domains during the cell cycle
title_sort possible role of drosophila ctcf in mitotic bookmarking and maintaining chromatin domains during the cell cycle
description BACKGROUND: The CCCTC-binding factor (CTCF) is a highly conserved insulator protein that plays various roles in many cellular processes. CTCF is one of the main architecture proteins in higher eukaryotes, and in combination with other architecture proteins and regulators, also shapes the three-dimensional organization of a genome. Experiments show CTCF partially remains associated with chromatin during mitosis. However, the role of CTCF in the maintenance and propagation of genome architectures throughout the cell cycle remains elusive. RESULTS: We performed a comprehensive bioinformatics analysis on public datasets of Drosophila CTCF (dCTCF). We characterized dCTCF-binding sites according to their occupancy status during the cell cycle, and identified three classes: interphase-mitosis-common (IM), interphase-only (IO) and mitosis-only (MO) sites. Integrated function analysis showed dCTCF-binding sites of different classes might be involved in different biological processes, and IM sites were more conserved and more intensely bound. dCTCF-binding sites of the same class preferentially localized closer to each other, and were highly enriched at chromatin syntenic and topologically associating domains boundaries. CONCLUSIONS: Our results revealed different functions of dCTCF during the cell cycle and suggested that dCTCF might contribute to the establishment of the three-dimensional architecture of the Drosophila genome by maintaining local chromatin compartments throughout the whole cell cycle.
publisher Sociedad de Biología de Chile
publishDate 2015
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602015000100027
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