A unified phylogeny-based nomenclature for histone variants

Paul B. Talbert(Howard Hughes Medical Institute), Kami Ahmad(Harvard University), Geneviève Almouzni(Centre National de la Recherche Scientifique), Juan Ausió(University of Victoria), Frédéric Berger(Temasek Life Sciences Laboratory), Prem L. Bhalla(The University of Melbourne), William M. Bonner, W. Zacheus Cande(University of California, Berkeley), Brian P. Chadwick(Florida State University), Wan Chan(University of California, Davis), George Cross(Rockefeller University), Liwang Cui(Pennsylvania State University), Stéfan Dimitrov(Inserm), Detlef Doenecke(University of Göttingen), José M. Eirín‐López(Universidade da Coruña), Martin A. Gorovsky(University of Rochester), Sandra B. Hake(Center for Integrated Protein Science Munich), Barbara A. Hamkalo(University of California, Irvine), Sarah Holec(Temasek Life Sciences Laboratory), Steven E. Jacobsen(Howard Hughes Medical Institute), Kinga Kamieniarz-Gdula(Max Planck Institute of Immunobiology and Epigenetics), Saadi Khochbin(Inserm), Andreas G. Ladurner(Ludwig-Maximilians-Universität München), David Landsman(National Center for Biotechnology Information), John Latham(Howard Hughes Medical Institute), Benjamin Loppin(Université Claude Bernard Lyon 1), Harmit S. Malik(Howard Hughes Medical Institute), William F. Marzluff(University of North Carolina at Chapel Hill), John R. Pehrson(University of Pennsylvania), Jan Postberg(Witten/Herdecke University), Robert J. Schneider(Institut de génétique et de biologie moléculaire et cellulaire), Mohan B. Singh(The University of Melbourne), M. Mitchell Smith(University of Virginia), Eric M. Thompson(University of Bergen), Maria‐Elena Torres‐Padilla(Centre National de la Recherche Scientifique), David J. Tremethick(Australian National University), Bryan M. Turner(University of Birmingham), Jakob H. Waterborg(University of Missouri–Kansas City), Heike Wollmann(Temasek Life Sciences Laboratory), Ramesh Yelagandula(Temasek Life Sciences Laboratory), Bing Zhu(National Institute of Biological Sciences, Beijing), Steven Henikoff(Howard Hughes Medical Institute)
Epigenetics & Chromatin
May 31, 2012
Cited by 344Open Access
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Abstract

Histone 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.


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