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dc.contributor.authorTalbert, Paul Beng
dc.contributor.authorAhmad, Kamieng
dc.contributor.authorAlmouzni, Genevièveeng
dc.contributor.authorAusió, Juaneng
dc.contributor.authorBerger, Fredericeng
dc.contributor.authorBhalla, Prem Leng
dc.contributor.authorBonner, William Meng
dc.contributor.authorCande, W Zeng
dc.contributor.authorChadwick, Brian Peng
dc.contributor.authorChan, Simon W Leng
dc.contributor.authorCross, George A Meng
dc.contributor.authorCui, Liwangeng
dc.contributor.authorDimitrov, Stefan Ieng
dc.contributor.authorDoenecke, Detlefeng
dc.contributor.authorEirin-López, José Meng
dc.contributor.authorGorovsky, Martin Aeng
dc.contributor.authorHake, Sandra Beng
dc.contributor.authorHamkalo, Barbara Aeng
dc.contributor.authorHolec, Saraheng
dc.contributor.authorJacobsen, Steven Eeng
dc.contributor.authorKamieniarz, Kingaeng
dc.contributor.authorKhochbin, Saadieng
dc.contributor.authorLadurner, Andreas Geng
dc.contributor.authorLandsman, Davideng
dc.contributor.authorLatham, John Aeng
dc.contributor.authorLoppin, Benjamineng
dc.contributor.authorMalik, Harmit Seng
dc.contributor.authorMarzluff, William Feng
dc.contributor.authorPehrson, John Reng
dc.contributor.authorPostberg, Janeng
dc.contributor.authorSchneider, Roberteng
dc.contributor.authorSingh, Mohan Beng
dc.contributor.authorSmith, M Meng
dc.contributor.authorThompson, Ericeng
dc.contributor.authorTorres-Padilla, Maria-Elenaeng
dc.contributor.authorTremethick, David Jeng
dc.contributor.authorTurner, Bryan Meng
dc.contributor.authorWaterborg, Jakob Heng
dc.contributor.authorWollmann, Heikeeng
dc.contributor.authorYelagandula, Ramesheng
dc.contributor.authorZhu, Bingeng
dc.contributor.authorHenikoff, Steveneng
dc.date.issued2012-05-31eng
dc.description.abstractAbstractHistone variants are non-allelic protein isoforms that play key roles in diversifying chromatin structure. The known number of such variants has greatly increased in recent years, but the lack of naming conventions for them has led to a variety of naming styles, multiple synonyms and misleading homographs that obscure variant relationships and complicate database searches. We propose here a unified nomenclature for variants of all five classes of histones that uses consistent but flexible naming conventions to produce names that are informative and readily searchable. The nomenclature builds on historical usage and incorporates phylogenetic relationships, which are strong predictors of structure and function. A key feature is the consistent use of punctuation to represent phylogenetic divergence, making explicit the relationships among variant subtypes that have previously been implicit or unclear. We recommend that by default new histone variants be named with organism-specific paralog-number suffixes that lack phylogenetic implication, while letter suffixes be reserved for structurally distinct clades of variants. For clarity and searchability, we encourage the use of descriptors that are separate from the phylogeny-based variant name to indicate developmental and other properties of variants that may be independent of structure.eng
dc.description.versionPeer Reviewedeng
dc.identifier.citationEpigenetics & Chromatin. 2012 May 31;5(1):7eng
dc.identifier.urihttp://dx.doi.org/10.1186/1756-8935-5-7eng
dc.identifier.urihttp://hdl.handle.net/10355/14734eng
dc.rights.holderPaul B Talbert et al.; licensee BioMed Central Ltd.eng
dc.titleA unified phylogeny-based nomenclature for histone variantseng
dc.typeJournal Articleeng


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