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Condensin II Regulates Interphase Chromatin Organization Through the Mrg-Binding Motif of Cap-H2

The spatial organization of the genome within the eukaryotic nucleus is a dynamic process that plays a central role in cellular processes such as gene expression, DNA replication, and chromosome segregation. Condensins are conserved multi-subunit protein complexes that contribute to chromosome organ...

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Autores principales: Wallace, Heather A., Klebba, Joseph E., Kusch, Thomas, Rogers, Gregory C., Bosco, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426367/
https://www.ncbi.nlm.nih.gov/pubmed/25758823
http://dx.doi.org/10.1534/g3.115.016634
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author Wallace, Heather A.
Klebba, Joseph E.
Kusch, Thomas
Rogers, Gregory C.
Bosco, Giovanni
author_facet Wallace, Heather A.
Klebba, Joseph E.
Kusch, Thomas
Rogers, Gregory C.
Bosco, Giovanni
author_sort Wallace, Heather A.
collection PubMed
description The spatial organization of the genome within the eukaryotic nucleus is a dynamic process that plays a central role in cellular processes such as gene expression, DNA replication, and chromosome segregation. Condensins are conserved multi-subunit protein complexes that contribute to chromosome organization by regulating chromosome compaction and homolog pairing. Previous work in our laboratory has shown that the Cap-H2 subunit of condensin II physically and genetically interacts with the Drosophila homolog of human MORF4-related gene on chromosome 15 (MRG15). Like Cap-H2, Mrg15 is required for interphase chromosome compaction and homolog pairing. However, the mechanism by which Mrg15 and Cap-H2 cooperate to maintain interphase chromatin organization remains unclear. Here, we show that Cap-H2 localizes to interband regions on polytene chromosomes and co-localizes with Mrg15 at regions of active transcription across the genome. We show that co-localization of Cap-H2 on polytene chromosomes is partially dependent on Mrg15. We have identified a binding motif within Cap-H2 that is essential for its interaction with Mrg15, and have found that mutation of this motif results in loss of localization of Cap-H2 on polytene chromosomes and results in partial suppression of Cap-H2-mediated compaction and homolog unpairing. Our data are consistent with a model in which Mrg15 acts as a loading factor to facilitate Cap-H2 binding to chromatin and mediate changes in chromatin organization.
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spelling pubmed-44263672015-05-13 Condensin II Regulates Interphase Chromatin Organization Through the Mrg-Binding Motif of Cap-H2 Wallace, Heather A. Klebba, Joseph E. Kusch, Thomas Rogers, Gregory C. Bosco, Giovanni G3 (Bethesda) Investigations The spatial organization of the genome within the eukaryotic nucleus is a dynamic process that plays a central role in cellular processes such as gene expression, DNA replication, and chromosome segregation. Condensins are conserved multi-subunit protein complexes that contribute to chromosome organization by regulating chromosome compaction and homolog pairing. Previous work in our laboratory has shown that the Cap-H2 subunit of condensin II physically and genetically interacts with the Drosophila homolog of human MORF4-related gene on chromosome 15 (MRG15). Like Cap-H2, Mrg15 is required for interphase chromosome compaction and homolog pairing. However, the mechanism by which Mrg15 and Cap-H2 cooperate to maintain interphase chromatin organization remains unclear. Here, we show that Cap-H2 localizes to interband regions on polytene chromosomes and co-localizes with Mrg15 at regions of active transcription across the genome. We show that co-localization of Cap-H2 on polytene chromosomes is partially dependent on Mrg15. We have identified a binding motif within Cap-H2 that is essential for its interaction with Mrg15, and have found that mutation of this motif results in loss of localization of Cap-H2 on polytene chromosomes and results in partial suppression of Cap-H2-mediated compaction and homolog unpairing. Our data are consistent with a model in which Mrg15 acts as a loading factor to facilitate Cap-H2 binding to chromatin and mediate changes in chromatin organization. Genetics Society of America 2015-03-09 /pmc/articles/PMC4426367/ /pubmed/25758823 http://dx.doi.org/10.1534/g3.115.016634 Text en Copyright © 2015 Wallace et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Wallace, Heather A.
Klebba, Joseph E.
Kusch, Thomas
Rogers, Gregory C.
Bosco, Giovanni
Condensin II Regulates Interphase Chromatin Organization Through the Mrg-Binding Motif of Cap-H2
title Condensin II Regulates Interphase Chromatin Organization Through the Mrg-Binding Motif of Cap-H2
title_full Condensin II Regulates Interphase Chromatin Organization Through the Mrg-Binding Motif of Cap-H2
title_fullStr Condensin II Regulates Interphase Chromatin Organization Through the Mrg-Binding Motif of Cap-H2
title_full_unstemmed Condensin II Regulates Interphase Chromatin Organization Through the Mrg-Binding Motif of Cap-H2
title_short Condensin II Regulates Interphase Chromatin Organization Through the Mrg-Binding Motif of Cap-H2
title_sort condensin ii regulates interphase chromatin organization through the mrg-binding motif of cap-h2
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426367/
https://www.ncbi.nlm.nih.gov/pubmed/25758823
http://dx.doi.org/10.1534/g3.115.016634
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