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The preRC protein ORCA organizes heterochromatin by assembling histone H3 lysine 9 methyltransferases on chromatin
Heterochromatic domains are enriched with repressive histone marks, including histone H3 lysine 9 methylation, written by lysine methyltransferases (KMTs). The pre-replication complex protein, origin recognition complex-associated (ORCA/LRWD1), preferentially localizes to heterochromatic regions in...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4442312/ https://www.ncbi.nlm.nih.gov/pubmed/25922909 http://dx.doi.org/10.7554/eLife.06496 |
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author | Giri, Sumanprava Aggarwal, Vasudha Pontis, Julien Shen, Zhen Chakraborty, Arindam Khan, Abid Mizzen, Craig Prasanth, Kannanganattu V Ait-Si-Ali, Slimane Ha, Taekjip Prasanth, Supriya G |
author_facet | Giri, Sumanprava Aggarwal, Vasudha Pontis, Julien Shen, Zhen Chakraborty, Arindam Khan, Abid Mizzen, Craig Prasanth, Kannanganattu V Ait-Si-Ali, Slimane Ha, Taekjip Prasanth, Supriya G |
author_sort | Giri, Sumanprava |
collection | PubMed |
description | Heterochromatic domains are enriched with repressive histone marks, including histone H3 lysine 9 methylation, written by lysine methyltransferases (KMTs). The pre-replication complex protein, origin recognition complex-associated (ORCA/LRWD1), preferentially localizes to heterochromatic regions in post-replicated cells. Its role in heterochromatin organization remained elusive. ORCA recognizes methylated H3K9 marks and interacts with repressive KMTs, including G9a/GLP and Suv39H1 in a chromatin context-dependent manner. Single-molecule pull-down assays demonstrate that ORCA-ORC (Origin Recognition Complex) and multiple H3K9 KMTs exist in a single complex and that ORCA stabilizes H3K9 KMT complex. Cells lacking ORCA show alterations in chromatin architecture, with significantly reduced H3K9 di- and tri-methylation at specific chromatin sites. Changes in heterochromatin structure due to loss of ORCA affect replication timing, preferentially at the late-replicating regions. We demonstrate that ORCA acts as a scaffold for the establishment of H3K9 KMT complex and its association and activity at specific chromatin sites is crucial for the organization of heterochromatin structure. DOI: http://dx.doi.org/10.7554/eLife.06496.001 |
format | Online Article Text |
id | pubmed-4442312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44423122015-05-26 The preRC protein ORCA organizes heterochromatin by assembling histone H3 lysine 9 methyltransferases on chromatin Giri, Sumanprava Aggarwal, Vasudha Pontis, Julien Shen, Zhen Chakraborty, Arindam Khan, Abid Mizzen, Craig Prasanth, Kannanganattu V Ait-Si-Ali, Slimane Ha, Taekjip Prasanth, Supriya G eLife Cell Biology Heterochromatic domains are enriched with repressive histone marks, including histone H3 lysine 9 methylation, written by lysine methyltransferases (KMTs). The pre-replication complex protein, origin recognition complex-associated (ORCA/LRWD1), preferentially localizes to heterochromatic regions in post-replicated cells. Its role in heterochromatin organization remained elusive. ORCA recognizes methylated H3K9 marks and interacts with repressive KMTs, including G9a/GLP and Suv39H1 in a chromatin context-dependent manner. Single-molecule pull-down assays demonstrate that ORCA-ORC (Origin Recognition Complex) and multiple H3K9 KMTs exist in a single complex and that ORCA stabilizes H3K9 KMT complex. Cells lacking ORCA show alterations in chromatin architecture, with significantly reduced H3K9 di- and tri-methylation at specific chromatin sites. Changes in heterochromatin structure due to loss of ORCA affect replication timing, preferentially at the late-replicating regions. We demonstrate that ORCA acts as a scaffold for the establishment of H3K9 KMT complex and its association and activity at specific chromatin sites is crucial for the organization of heterochromatin structure. DOI: http://dx.doi.org/10.7554/eLife.06496.001 eLife Sciences Publications, Ltd 2015-04-29 /pmc/articles/PMC4442312/ /pubmed/25922909 http://dx.doi.org/10.7554/eLife.06496 Text en © 2015, Giri et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Giri, Sumanprava Aggarwal, Vasudha Pontis, Julien Shen, Zhen Chakraborty, Arindam Khan, Abid Mizzen, Craig Prasanth, Kannanganattu V Ait-Si-Ali, Slimane Ha, Taekjip Prasanth, Supriya G The preRC protein ORCA organizes heterochromatin by assembling histone H3 lysine 9 methyltransferases on chromatin |
title | The preRC protein ORCA organizes heterochromatin by assembling histone H3 lysine 9 methyltransferases on chromatin |
title_full | The preRC protein ORCA organizes heterochromatin by assembling histone H3 lysine 9 methyltransferases on chromatin |
title_fullStr | The preRC protein ORCA organizes heterochromatin by assembling histone H3 lysine 9 methyltransferases on chromatin |
title_full_unstemmed | The preRC protein ORCA organizes heterochromatin by assembling histone H3 lysine 9 methyltransferases on chromatin |
title_short | The preRC protein ORCA organizes heterochromatin by assembling histone H3 lysine 9 methyltransferases on chromatin |
title_sort | prerc protein orca organizes heterochromatin by assembling histone h3 lysine 9 methyltransferases on chromatin |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4442312/ https://www.ncbi.nlm.nih.gov/pubmed/25922909 http://dx.doi.org/10.7554/eLife.06496 |
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