Mammalian HP1 isoforms have specific roles in heterochromatin structure and organization

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  • dc.contributor.author Bosch Presegué, Laiaca
  • dc.contributor.author Raurell Vila, Helenaca
  • dc.contributor.author Thackray, Joshua K.ca
  • dc.contributor.author González, Jessicaca
  • dc.contributor.author Casal, Carmenca
  • dc.contributor.author Kane-Goldsmith, Norikoca
  • dc.contributor.author Vizoso, Miguelca
  • dc.contributor.author Brown, Jeremy P.ca
  • dc.contributor.author Gómez, Antonioca
  • dc.contributor.author Ausió, Juanca
  • dc.contributor.author Zimmermann, Timoca
  • dc.contributor.author Esteller, Manelca
  • dc.contributor.author Schotta, Gunnarca
  • dc.contributor.author Singh, Prim B.ca
  • dc.contributor.author Serrano, Lourdesca
  • dc.contributor.author Vaquero, Alejandroca
  • dc.date.accessioned 2018-05-24T07:54:29Z
  • dc.date.available 2018-05-24T07:54:29Z
  • dc.date.issued 2017
  • dc.description.abstract HP1 is a structural component of heterochromatin. Mammalian HP1 isoforms HP1α, HP1β, and HP1γ play different roles in genome stability, but their precise role in heterochromatin structure is unclear. Analysis of Hp1α-/-, Hp1β-/-, and Hp1γ-/- MEFs show that HP1 proteins have both redundant and unique functions within pericentric heterochromatin (PCH) and also act globally throughout the genome. HP1α confines H4K20me3 and H3K27me3 to regions within PCH, while its absence results in a global hyper-compaction of chromatin associated with a specific pattern of mitotic defects. In contrast, HP1β is functionally associated with Suv4-20h2 and H4K20me3, and its loss induces global chromatin decompaction and an abnormal enrichment of CTCF in PCH and other genomic regions. Our work provides insight into the roles of HP1 proteins in heterochromatin structure and genome stability.
  • dc.description.sponsorship This work was supported by the Spanish Ministry of Economy and Competitiveness (MINECO) (SAF2011-25860 and SAF2014-55964R to A.V.) and cofunded by FEDER funds/European Regional Development Fund (ERDF)-a way to build Europe, the Catalan Government Agency AGAUR (2009SGR-914 and 2014SGR-400 to A.V.), HGINJ (to L.S.), Deutsche Forschungsgemeinschaft (SFB1064 to G.S.), and the Canadian Institutes of Health Research (CIHR) (MOP-97878 to J.A.).
  • dc.format.mimetype application/pdf
  • dc.identifier.citation Bosch-Presegué L, Raurell-Vila H, Thackray JK, González J, Casal C, Kane-Goldsmith N et al. Mammalian HP1 Isoforms Have Specific Roles in Heterochromatin Structure and Organization. Cell Reports 2017 Nov; 21(8): 2048-2057. DOI: 10.1016/j.celrep.2017.10.092
  • dc.identifier.doi http://dx.doi.org/10.1016/j.celrep.2017.10.092
  • dc.identifier.issn 2211-1247
  • dc.identifier.uri http://hdl.handle.net/10230/34717
  • dc.language.iso eng
  • dc.publisher Elsevierca
  • dc.relation.ispartof Cell Reports 2017 Nov; 21(8): 2048-2057
  • dc.relation.projectID info:eu-repo/grantAgreement/ES/3PN/SAF2011-25860
  • dc.relation.projectID info:eu-repo/grantAgreement/ES/1PE/SAF2014-55964-R
  • dc.rights © 2017 The Authors. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
  • dc.rights.accessRights info:eu-repo/semantics/openAccess
  • dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/4.0/
  • dc.subject.keyword H4K20me3
  • dc.subject.keyword HP1α
  • dc.subject.keyword HP1β
  • dc.subject.keyword HP1γ
  • dc.subject.keyword Suv420h2
  • dc.subject.keyword Genome organization
  • dc.subject.keyword Genome stability
  • dc.subject.keyword Heterochromatin
  • dc.title Mammalian HP1 isoforms have specific roles in heterochromatin structure and organizationca
  • dc.type info:eu-repo/semantics/article
  • dc.type.version info:eu-repo/semantics/publishedVersion