Probabilistic establishment of speckle-associated inter-chromosomal interactions

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dc.contributor.authorJoo, Jaegeonko
dc.contributor.authorCho, Sunghyunko
dc.contributor.authorHong, Sukbumko
dc.contributor.authorMin, Sunwooko
dc.contributor.authorKim, Kyukwangko
dc.contributor.authorKumar, Rajeevko
dc.contributor.authorChoi, Jeong-Moko
dc.contributor.authorShin, Yongdaeko
dc.contributor.authorJung, Inkyungko
dc.date.accessioned2023-07-02T00:00:26Z-
dc.date.available2023-07-02T00:00:26Z-
dc.date.created2023-04-24-
dc.date.created2023-04-24-
dc.date.created2023-04-24-
dc.date.created2023-04-24-
dc.date.issued2023-06-
dc.identifier.citationNUCLEIC ACIDS RESEARCH, v.51, no.11, pp.5377 - 5395-
dc.identifier.issn0305-1048-
dc.identifier.urihttp://hdl.handle.net/10203/310181-
dc.description.abstractInter-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.-
dc.languageEnglish-
dc.publisherOXFORD UNIV PRESS-
dc.titleProbabilistic establishment of speckle-associated inter-chromosomal interactions-
dc.typeArticle-
dc.identifier.wosid000962422600001-
dc.identifier.scopusid2-s2.0-85163967163-
dc.type.rimsART-
dc.citation.volume51-
dc.citation.issue11-
dc.citation.beginningpage5377-
dc.citation.endingpage5395-
dc.citation.publicationnameNUCLEIC ACIDS RESEARCH-
dc.identifier.doi10.1093/nar/gkad211-
dc.contributor.localauthorJung, Inkyung-
dc.contributor.nonIdAuthorCho, Sunghyun-
dc.contributor.nonIdAuthorHong, Sukbum-
dc.contributor.nonIdAuthorKumar, Rajeev-
dc.contributor.nonIdAuthorChoi, Jeong-Mo-
dc.contributor.nonIdAuthorShin, Yongdae-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusCELL IDENTITY-
dc.subject.keywordPlusHUMAN GENOME-
dc.subject.keywordPlusTRANSCRIPTION FACTORS-
dc.subject.keywordPlusSUPER-ENHANCERS-
dc.subject.keywordPlusHI-C-
dc.subject.keywordPlusCHROMATIN-
dc.subject.keywordPlusDOMAINS-
dc.subject.keywordPlusORGANIZATION-
dc.subject.keywordPlusPRINCIPLES-
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