Probabilistic establishment of speckle-associated inter-chromosomal interactions
Abstract Inter-chromosomal interactions play a crucial role in genome organization, yet the organizational principles remain elusive. Here, we introduce a novel computational method to systematically characterize inter-chromosomal interactions using in situ Hi-C results from various cell types. Our...
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Veröffentlicht in: | Nucleic acids research 2023-06, Vol.51 (11), p.5377-5395 |
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creator | Joo, Jaegeon Cho, Sunghyun Hong, Sukbum Min, Sunwoo Kim, Kyukwang Kumar, Rajeev Choi, Jeong-Mo Shin, Yongdae Jung, Inkyung |
description | Abstract
Inter-chromosomal interactions play a crucial role in genome organization, yet the organizational principles remain elusive. Here, we introduce a novel computational method to systematically characterize inter-chromosomal interactions using in situ Hi-C results from various cell types. Our method successfully identifies two apparently hub-like inter-chromosomal contacts associated with nuclear speckles and nucleoli, respectively. Interestingly, we discover that nuclear speckle-associated inter-chromosomal interactions are highly cell-type invariant with a marked enrichment of cell-type common super-enhancers (CSEs). Validation using DNA Oligopaint fluorescence in situ hybridization (FISH) shows a strong but probabilistic interaction behavior between nuclear speckles and CSE-harboring genomic regions. Strikingly, we find that the likelihood of speckle-CSE associations can accurately predict two experimentally measured inter-chromosomal contacts from Hi-C and Oligopaint DNA FISH. Our probabilistic establishment model well describes the hub-like structure observed at the population level as a cumulative effect of summing individual stochastic chromatin-speckle interactions. Lastly, we observe that CSEs are highly co-occupied by MAZ binding and MAZ depletion leads to significant disorganization of speckle-associated inter-chromosomal contacts. Taken together, our results propose a simple organizational principle of inter-chromosomal interactions mediated by MAZ-occupied CSEs. |
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Inter-chromosomal interactions play a crucial role in genome organization, yet the organizational principles remain elusive. Here, we introduce a novel computational method to systematically characterize inter-chromosomal interactions using in situ Hi-C results from various cell types. Our method successfully identifies two apparently hub-like inter-chromosomal contacts associated with nuclear speckles and nucleoli, respectively. Interestingly, we discover that nuclear speckle-associated inter-chromosomal interactions are highly cell-type invariant with a marked enrichment of cell-type common super-enhancers (CSEs). Validation using DNA Oligopaint fluorescence in situ hybridization (FISH) shows a strong but probabilistic interaction behavior between nuclear speckles and CSE-harboring genomic regions. Strikingly, we find that the likelihood of speckle-CSE associations can accurately predict two experimentally measured inter-chromosomal contacts from Hi-C and Oligopaint DNA FISH. Our probabilistic establishment model well describes the hub-like structure observed at the population level as a cumulative effect of summing individual stochastic chromatin-speckle interactions. Lastly, we observe that CSEs are highly co-occupied by MAZ binding and MAZ depletion leads to significant disorganization of speckle-associated inter-chromosomal contacts. Taken together, our results propose a simple organizational principle of inter-chromosomal interactions mediated by MAZ-occupied CSEs.</description><identifier>ISSN: 0305-1048</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/gkad211</identifier><identifier>PMID: 37013988</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Cell Nucleus - metabolism ; Chromatin - genetics ; Chromatin - metabolism ; Chromosomes ; DNA - genetics ; DNA - metabolism ; Gene regulation, Chromatin and Epigenetics ; Humans ; In Situ Hybridization, Fluorescence</subject><ispartof>Nucleic acids research, 2023-06, Vol.51 (11), p.5377-5395</ispartof><rights>The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. 2023</rights><rights>The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c413t-ce896a7128019500497c6b67109d99272c04c12b04f8120f7f30351beecad98d3</citedby><cites>FETCH-LOGICAL-c413t-ce896a7128019500497c6b67109d99272c04c12b04f8120f7f30351beecad98d3</cites><orcidid>0000-0003-2656-4851 ; 0000-0002-5885-2754 ; 0000-0003-3441-1986</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287923/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287923/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,1604,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37013988$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Joo, Jaegeon</creatorcontrib><creatorcontrib>Cho, Sunghyun</creatorcontrib><creatorcontrib>Hong, Sukbum</creatorcontrib><creatorcontrib>Min, Sunwoo</creatorcontrib><creatorcontrib>Kim, Kyukwang</creatorcontrib><creatorcontrib>Kumar, Rajeev</creatorcontrib><creatorcontrib>Choi, Jeong-Mo</creatorcontrib><creatorcontrib>Shin, Yongdae</creatorcontrib><creatorcontrib>Jung, Inkyung</creatorcontrib><title>Probabilistic establishment of speckle-associated inter-chromosomal interactions</title><title>Nucleic acids research</title><addtitle>Nucleic Acids Res</addtitle><description>Abstract
Inter-chromosomal interactions play a crucial role in genome organization, yet the organizational principles remain elusive. Here, we introduce a novel computational method to systematically characterize inter-chromosomal interactions using in situ Hi-C results from various cell types. Our method successfully identifies two apparently hub-like inter-chromosomal contacts associated with nuclear speckles and nucleoli, respectively. Interestingly, we discover that nuclear speckle-associated inter-chromosomal interactions are highly cell-type invariant with a marked enrichment of cell-type common super-enhancers (CSEs). Validation using DNA Oligopaint fluorescence in situ hybridization (FISH) shows a strong but probabilistic interaction behavior between nuclear speckles and CSE-harboring genomic regions. Strikingly, we find that the likelihood of speckle-CSE associations can accurately predict two experimentally measured inter-chromosomal contacts from Hi-C and Oligopaint DNA FISH. Our probabilistic establishment model well describes the hub-like structure observed at the population level as a cumulative effect of summing individual stochastic chromatin-speckle interactions. Lastly, we observe that CSEs are highly co-occupied by MAZ binding and MAZ depletion leads to significant disorganization of speckle-associated inter-chromosomal contacts. Taken together, our results propose a simple organizational principle of inter-chromosomal interactions mediated by MAZ-occupied CSEs.</description><subject>Cell Nucleus - metabolism</subject><subject>Chromatin - genetics</subject><subject>Chromatin - metabolism</subject><subject>Chromosomes</subject><subject>DNA - genetics</subject><subject>DNA - metabolism</subject><subject>Gene regulation, Chromatin and Epigenetics</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><sourceid>EIF</sourceid><recordid>eNp9kctLAzEQxoMotlZP3qUnEWTtTLKP5CRSfEHBHvQcstlsG7u7qclW8L830ip68TTDzI9vHh8hpwhXCIJNOuUni5WqKOIeGSLLaZKKnO6TITDIEoSUD8hRCK8AmGKWHpIBKwCZ4HxI5nPvSlXaxobe6rEJvSpjvmxN149dPQ5ro1eNSVQITlvVm2psu974RC-9a11wrWq2FaV767pwTA5q1QRzsosj8nJ3-zx9SGZP94_Tm1miU2R9og0XuSqQckCRAaSi0HmZF_GiSghaUA2pRlpCWnOkUBc1A5ZhaYxWleAVG5Hrre56U7am0nFfrxq59rZV_kM6ZeXfTmeXcuHeJQLlhaAsKlzsFLx728TLZWuDNk2jOuM2QdJCZCzjOWQRvdyi2rsQvKl_5iDILxNkNEHuTIj02e_Vftjvr0fgfAu4zfpfpU_PyJKd</recordid><startdate>20230623</startdate><enddate>20230623</enddate><creator>Joo, Jaegeon</creator><creator>Cho, Sunghyun</creator><creator>Hong, Sukbum</creator><creator>Min, Sunwoo</creator><creator>Kim, Kyukwang</creator><creator>Kumar, Rajeev</creator><creator>Choi, Jeong-Mo</creator><creator>Shin, Yongdae</creator><creator>Jung, Inkyung</creator><general>Oxford University Press</general><scope>TOX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2656-4851</orcidid><orcidid>https://orcid.org/0000-0002-5885-2754</orcidid><orcidid>https://orcid.org/0000-0003-3441-1986</orcidid></search><sort><creationdate>20230623</creationdate><title>Probabilistic establishment of speckle-associated inter-chromosomal interactions</title><author>Joo, Jaegeon ; Cho, Sunghyun ; Hong, Sukbum ; Min, Sunwoo ; Kim, Kyukwang ; Kumar, Rajeev ; Choi, Jeong-Mo ; Shin, Yongdae ; Jung, Inkyung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-ce896a7128019500497c6b67109d99272c04c12b04f8120f7f30351beecad98d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Cell Nucleus - metabolism</topic><topic>Chromatin - genetics</topic><topic>Chromatin - metabolism</topic><topic>Chromosomes</topic><topic>DNA - genetics</topic><topic>DNA - metabolism</topic><topic>Gene regulation, Chromatin and Epigenetics</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Joo, Jaegeon</creatorcontrib><creatorcontrib>Cho, Sunghyun</creatorcontrib><creatorcontrib>Hong, Sukbum</creatorcontrib><creatorcontrib>Min, Sunwoo</creatorcontrib><creatorcontrib>Kim, Kyukwang</creatorcontrib><creatorcontrib>Kumar, Rajeev</creatorcontrib><creatorcontrib>Choi, Jeong-Mo</creatorcontrib><creatorcontrib>Shin, Yongdae</creatorcontrib><creatorcontrib>Jung, Inkyung</creatorcontrib><collection>Access via Oxford University Press (Open Access Collection)</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nucleic acids research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Joo, Jaegeon</au><au>Cho, Sunghyun</au><au>Hong, Sukbum</au><au>Min, Sunwoo</au><au>Kim, Kyukwang</au><au>Kumar, Rajeev</au><au>Choi, Jeong-Mo</au><au>Shin, Yongdae</au><au>Jung, Inkyung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Probabilistic establishment of speckle-associated inter-chromosomal interactions</atitle><jtitle>Nucleic acids research</jtitle><addtitle>Nucleic Acids Res</addtitle><date>2023-06-23</date><risdate>2023</risdate><volume>51</volume><issue>11</issue><spage>5377</spage><epage>5395</epage><pages>5377-5395</pages><issn>0305-1048</issn><eissn>1362-4962</eissn><abstract>Abstract
Inter-chromosomal interactions play a crucial role in genome organization, yet the organizational principles remain elusive. Here, we introduce a novel computational method to systematically characterize inter-chromosomal interactions using in situ Hi-C results from various cell types. Our method successfully identifies two apparently hub-like inter-chromosomal contacts associated with nuclear speckles and nucleoli, respectively. Interestingly, we discover that nuclear speckle-associated inter-chromosomal interactions are highly cell-type invariant with a marked enrichment of cell-type common super-enhancers (CSEs). Validation using DNA Oligopaint fluorescence in situ hybridization (FISH) shows a strong but probabilistic interaction behavior between nuclear speckles and CSE-harboring genomic regions. Strikingly, we find that the likelihood of speckle-CSE associations can accurately predict two experimentally measured inter-chromosomal contacts from Hi-C and Oligopaint DNA FISH. Our probabilistic establishment model well describes the hub-like structure observed at the population level as a cumulative effect of summing individual stochastic chromatin-speckle interactions. Lastly, we observe that CSEs are highly co-occupied by MAZ binding and MAZ depletion leads to significant disorganization of speckle-associated inter-chromosomal contacts. Taken together, our results propose a simple organizational principle of inter-chromosomal interactions mediated by MAZ-occupied CSEs.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>37013988</pmid><doi>10.1093/nar/gkad211</doi><tpages>19</tpages><orcidid>https://orcid.org/0000-0003-2656-4851</orcidid><orcidid>https://orcid.org/0000-0002-5885-2754</orcidid><orcidid>https://orcid.org/0000-0003-3441-1986</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Cell Nucleus - metabolism Chromatin - genetics Chromatin - metabolism Chromosomes DNA - genetics DNA - metabolism Gene regulation, Chromatin and Epigenetics Humans In Situ Hybridization, Fluorescence |
title | Probabilistic establishment of speckle-associated inter-chromosomal interactions |
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