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dc.contributor.authorGahan, James
dc.contributor.authorRentzsch, Fabian
dc.contributor.authorSchnitzler, Christine E.
dc.date.accessioned2021-05-07T12:16:47Z
dc.date.available2021-05-07T12:16:47Z
dc.date.created2020-11-25T13:14:25Z
dc.date.issued2020
dc.PublishedProceedings of the National Academy of Sciences of the United States of America. 2020, 117 (37), 22880-22889.
dc.identifier.issn0027-8424
dc.identifier.urihttps://hdl.handle.net/11250/2754177
dc.description.abstractPolycomb group proteins are essential regulators of developmental processes across animals. Despite their importance, studies on Polycomb are often restricted to classical model systems and, as such, little is known about the evolution of these important chromatin regulators. Here we focus on Polycomb Repressive Complex 1 (PRC1) and trace the evolution of core components of canonical and non-canonical PRC1 complexes in animals. Previous work suggested that a major expansion in the number of PRC1 complexes occurred in the vertebrate lineage. We show that the expansion of the Polycomb Group RING Finger (PCGF) protein family, an essential step for the establishment of the large diversity of PRC1 complexes found in vertebrates, predates the bilaterian–cnidarian ancestor. This means that the genetic repertoire necessary to form all major vertebrate PRC1 complexes emerged early in animal evolution, over 550 million years ago. We further show that PCGF5, a gene conserved in cnidarians and vertebrates but lost in all other studied groups, is expressed in the nervous system in the sea anemone Nematostella vectensis, similar to its mammalian counterpart. Together this work provides a framework for understanding the evolution of PRC1 complex diversity and it establishes Nematostella as a promising model system in which the functional ramifications of this diversification can be further explored.en_US
dc.language.isoengen_US
dc.publisherNational Academy of Sciencesen_US
dc.titleThe genetic basis for PRC1 complex diversity emerged early in animal evolutionen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionacceptedVersionen_US
dc.rights.holderCopyright 2020 The Authorsen_US
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2
dc.identifier.doi10.1073/pnas.2005136117
dc.identifier.cristin1852215
dc.source.journalProceedings of the National Academy of Sciences of the United States of Americaen_US
dc.source.40117
dc.source.1437
dc.source.pagenumber22880-22889en_US
dc.identifier.citationProceedings of the National Academy of Sciences of the United States of America. 2020, 117 (37), 22880-22889en_US
dc.source.volume117en_US
dc.source.issue37en_US


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