Matches in SemOpenAlex for { <https://semopenalex.org/work/W1925859908> ?p ?o ?g. }
- W1925859908 endingPage "527" @default.
- W1925859908 startingPage "516" @default.
- W1925859908 abstract "•Canonical histone proteins are replaced with specific variants before and during periods of cellular transition. •Histone variants regulate cellular plasticity during development and in the adult nervous system. •Variants TH2A, TH2B, H2A.Z, and H3.3 facilitate cellular plasticity in early development. •Variants H2A.X, H3.3, and macroH2A inhibit developmental plasticity following cellular differentiation. •Variants H3.3, H2A.Z, and H2B.E regulate cellular plasticity in the adult nervous system. The broad diversity of cell types within vertebrates arises from a unique genetic blueprint by combining intrinsic cellular information with developmental and other extrinsic signals. Lying at the interface between cellular signals and the DNA is the chromatin, a dynamic nucleoprotein complex that helps to mediate gene regulation. The most basic subunit of chromatin, the nucleosome, consists of DNA wrapped around histones, a set of proteins that play crucial roles as scaffolding molecules and regulators of gene expression. Growing evidence indicates that canonical histones are commonly replaced by protein variants before and during cellular transitions. We highlight exciting new results suggesting that histone variants are essential players in the control of cellular plasticity during development and in the adult nervous system. The broad diversity of cell types within vertebrates arises from a unique genetic blueprint by combining intrinsic cellular information with developmental and other extrinsic signals. Lying at the interface between cellular signals and the DNA is the chromatin, a dynamic nucleoprotein complex that helps to mediate gene regulation. The most basic subunit of chromatin, the nucleosome, consists of DNA wrapped around histones, a set of proteins that play crucial roles as scaffolding molecules and regulators of gene expression. Growing evidence indicates that canonical histones are commonly replaced by protein variants before and during cellular transitions. We highlight exciting new results suggesting that histone variants are essential players in the control of cellular plasticity during development and in the adult nervous system. region of chromatin that contains both activating and repressive modifications, and is thus silent but poised for potential future activation. cell derived from the inner cell mass of a blastocyst (an early-stage embryo) that is pluripotent and can be grown indefinitely in culture. nucleosome that contains one copy of a particular histone variant and one copy of a canonical histone from the same family. covalent chemical modification of a histone protein that affects its structure and function. five families of positively charged proteins (H1, H2A, H2B, H3, and H4) that package DNA into nucleosomes within eukaryotic cell nuclei and play central roles in regulating gene expression. non-allelic isoform of a canonical histone protein. nucleosome that contains two copies of a particular histone variant. nucleosome that contains multiple distinct histone variants. the ability of a cell to divide and produce more than one differentiated cell type. electrical and chemical signaling that occurs upon activation of neuronal receptors. process in which a differentiated cell is converted to pluripotency. the basic unit of chromatin in eukaryotes, consisting of DNA wrapped around an octamer of histone proteins (two subunits from each of the H2A, H2B, H3, and H4 families). the ability of a cell to divide and produce all of the differentiated cell types in an organism. phase (‘synthesis’) of the cell cycle in which DNA is replicated and packaged largely with canonical histones. process in which the nucleus from a differentiated cell is reprogrammed following transfer to an oocyte." @default.
- W1925859908 created "2016-06-24" @default.
- W1925859908 creator A5079218238 @default.
- W1925859908 creator A5089691588 @default.
- W1925859908 date "2015-09-01" @default.
- W1925859908 modified "2023-10-16" @default.
- W1925859908 title "Histone variants and cellular plasticity" @default.
- W1925859908 cites W1525654309 @default.
- W1925859908 cites W1537559146 @default.
- W1925859908 cites W1579352208 @default.
- W1925859908 cites W1587848884 @default.
- W1925859908 cites W1588343997 @default.
- W1925859908 cites W165264651 @default.
- W1925859908 cites W1755602580 @default.
- W1925859908 cites W1793067559 @default.
- W1925859908 cites W1822988701 @default.
- W1925859908 cites W1963771535 @default.
- W1925859908 cites W1964480889 @default.
- W1925859908 cites W1966218941 @default.
- W1925859908 cites W1967835379 @default.
- W1925859908 cites W1968637358 @default.
- W1925859908 cites W1969638746 @default.
- W1925859908 cites W1970748830 @default.
- W1925859908 cites W1970916644 @default.
- W1925859908 cites W1976968160 @default.
- W1925859908 cites W1981088384 @default.
- W1925859908 cites W1988728880 @default.
- W1925859908 cites W1988997204 @default.
- W1925859908 cites W1991335608 @default.
- W1925859908 cites W1991978196 @default.
- W1925859908 cites W1992213480 @default.
- W1925859908 cites W1993069558 @default.
- W1925859908 cites W1993362950 @default.
- W1925859908 cites W1993891331 @default.
- W1925859908 cites W1995105508 @default.
- W1925859908 cites W2000943453 @default.
- W1925859908 cites W2001528712 @default.
- W1925859908 cites W2001780146 @default.
- W1925859908 cites W2002793113 @default.
- W1925859908 cites W2007243165 @default.
- W1925859908 cites W2007497552 @default.
- W1925859908 cites W2011285661 @default.
- W1925859908 cites W2012751802 @default.
- W1925859908 cites W2017704822 @default.
- W1925859908 cites W2017909805 @default.
- W1925859908 cites W2020790775 @default.
- W1925859908 cites W2022140142 @default.
- W1925859908 cites W2023798198 @default.
- W1925859908 cites W2025525406 @default.
- W1925859908 cites W2025708369 @default.
- W1925859908 cites W2028719532 @default.
- W1925859908 cites W2028927305 @default.
- W1925859908 cites W2037231961 @default.
- W1925859908 cites W2038356000 @default.
- W1925859908 cites W2043403539 @default.
- W1925859908 cites W2044021223 @default.
- W1925859908 cites W2044459308 @default.
- W1925859908 cites W2044727292 @default.
- W1925859908 cites W2048753655 @default.
- W1925859908 cites W2050445493 @default.
- W1925859908 cites W2050907834 @default.
- W1925859908 cites W2052436973 @default.
- W1925859908 cites W2053120614 @default.
- W1925859908 cites W2060924735 @default.
- W1925859908 cites W2062062519 @default.
- W1925859908 cites W2064565230 @default.
- W1925859908 cites W2065055088 @default.
- W1925859908 cites W2065530211 @default.
- W1925859908 cites W2072002750 @default.
- W1925859908 cites W2074998492 @default.
- W1925859908 cites W2076788485 @default.
- W1925859908 cites W2077313738 @default.
- W1925859908 cites W2078589960 @default.
- W1925859908 cites W2080578479 @default.
- W1925859908 cites W2081100502 @default.
- W1925859908 cites W2083245183 @default.
- W1925859908 cites W2083775070 @default.
- W1925859908 cites W2087476954 @default.
- W1925859908 cites W2087573417 @default.
- W1925859908 cites W2090948659 @default.
- W1925859908 cites W2091981381 @default.
- W1925859908 cites W2093519749 @default.
- W1925859908 cites W2094584847 @default.
- W1925859908 cites W2095491090 @default.
- W1925859908 cites W2097633421 @default.
- W1925859908 cites W2098103685 @default.
- W1925859908 cites W2099188975 @default.
- W1925859908 cites W2102419243 @default.
- W1925859908 cites W2102901123 @default.
- W1925859908 cites W2108547322 @default.
- W1925859908 cites W2111845989 @default.
- W1925859908 cites W2113743152 @default.
- W1925859908 cites W2115562886 @default.
- W1925859908 cites W2115656844 @default.
- W1925859908 cites W2119137351 @default.
- W1925859908 cites W2121876535 @default.
- W1925859908 cites W2123518376 @default.
- W1925859908 cites W2126806930 @default.