The characterization of macroH2A beyond vertebrates supports an ancestral origin and conserved role for histone variants in chromatin
Date of this Version
6-2016
Document Type
Article
Rights
default
Abstract
Histone variants play a critical role in chromatin structure and epigenetic regulation. These “deviant” proteins have been historically considered as the evolutionary descendants of ancestral canonical histones, helping specialize the nucleosome structure during eukaryotic evolution. Such view is now challenged by 2 major observations: first, canonical histones present extremely unique features not shared with any other genes; second, histone variants are widespread across many eukaryotic groups. The present work further supports the ancestral nature of histone variants by providing the first in vivo characterization of a functional macroH2A histone (a variant long defined as a specific refinement of vertebrate chromatin) in a non-vertebrate organism (the mussel Mytilus) revealing its recruitment into heterochromatic fractions of actively proliferating tissues. Combined with in silico analyses of genomic data, these results provide evidence for the widespread presence of macroH2A in metazoan animals, as well as in the holozoan Capsaspora, supporting an evolutionary origin for this histone variant lineage before the radiation of Filozoans (including Filasterea, Choanoflagellata and Metazoa). Overall, the results presented in this work help configure a new evolutionary scenario in which histone variants, rather than modern “deviants” of canonical histones, would constitute ancient components of eukaryotic chromatin.
Identifier
FIDC006331
Recommended Citation
Rivera-Casas, Ciro; Gonzalez-Romero, Rodrigo; Cheema, Manjinder S.; Ausio, Juan; and Eirin-Lopez, Jose M., "The characterization of macroH2A beyond vertebrates supports an ancestral origin and conserved role for histone variants in chromatin" (2016). Center for Coastal Oceans Research Faculty Publications. 6.
https://digitalcommons.fiu.edu/merc_fac/6
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Comments
Originally published in Epigenetics.