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Histone modifications and nuclear architecture: a review
E Bartova, J Krejci, A Harnicarova, G Galiova, S Kozubek
Jazyk angličtina Země Spojené státy americké
Typ dokumentu přehledy
NLK
Free Medical Journals
od 1953 do Před 1 rokem
SAGE Publications Journals
od 1999-01-01 do 2015-12-31
- MeSH
- acetylace MeSH
- buněčné jádro metabolismus ultrastruktura MeSH
- chromatin ultrastruktura MeSH
- chromozomální proteiny, nehistonové fyziologie MeSH
- epigeneze genetická MeSH
- exprese genu MeSH
- financování organizované MeSH
- histony genetika metabolismus MeSH
- interfáze MeSH
- lidé MeSH
- lidské chromozomy X metabolismus MeSH
- metylace MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- přehledy MeSH
Epigenetic modifications, such as acetylation, phosphorylation, methylation, ubiquitination, and ADP ribosylation, of the highly conserved core histones, H2A, H2B, H3, and H4, influence the genetic potential of DNA. The enormous regulatory potential of histone modification is illustrated in the vast array of epigenetic markers found throughout the genome. More than the other types of histone modification, acetylation and methylation of specific lysine residues on N-terminal histone tails are fundamental for the formation of chromatin domains, such as euchromatin, and facultative and constitutive heterochromatin. In addition, the modification of histones can cause a region of chromatin to undergo nuclear compartmentalization and, as such, specific epigenetic markers are non-randomly distributed within interphase nuclei. In this review, we summarize the principles behind epigenetic compartmentalization and the functional consequences of chromatin arrangement within interphase nuclei.
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- $a Laboratory of Molecular Cytology and Cytometry, Institute of Biophysics, Academy of Sciences of the Czech Republic, Brno, Czech Republic. bartova@ibp.cz
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- $a Epigenetic modifications, such as acetylation, phosphorylation, methylation, ubiquitination, and ADP ribosylation, of the highly conserved core histones, H2A, H2B, H3, and H4, influence the genetic potential of DNA. The enormous regulatory potential of histone modification is illustrated in the vast array of epigenetic markers found throughout the genome. More than the other types of histone modification, acetylation and methylation of specific lysine residues on N-terminal histone tails are fundamental for the formation of chromatin domains, such as euchromatin, and facultative and constitutive heterochromatin. In addition, the modification of histones can cause a region of chromatin to undergo nuclear compartmentalization and, as such, specific epigenetic markers are non-randomly distributed within interphase nuclei. In this review, we summarize the principles behind epigenetic compartmentalization and the functional consequences of chromatin arrangement within interphase nuclei.
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