Stop-and-Go: Dynamics of Nucleolar Transcription During the Cell Cycle.
H2AQ104 methylation
RNA polymerase I
SIRT7
acetylation
cell cycle
fibrillarin
rDNA
transcription
Journal
Epigenetics insights
ISSN: 2516-8657
Titre abrégé: Epigenet Insights
Pays: United States
ID NLM: 101735398
Informations de publication
Date de publication:
2019
2019
Historique:
received:
02
04
2019
accepted:
09
04
2019
entrez:
18
6
2019
pubmed:
18
6
2019
medline:
18
6
2019
Statut:
epublish
Résumé
Entry into mitosis correlates with nucleolar disassembly and shutdown of ribosomal RNA (rRNA) gene (rDNA) transcription. In telophase, nucleoli reform and transcription is reactivated. The molecular mechanisms underlying the dynamics of nucleolar transcription during the cell cycle are manifold. Although mitotic inactivation of the RNA polymerase I (Pol I) transcription machinery by posttranslational modifications has been extensively studied, little is known about the structure of rDNA chromatin during progression through mitosis. Methylation of histone H2A at glutamine 104 (H2AQ104me), a dedicated nucleolar histone modification, is lost in prometaphase, leading to chromatin compaction, which enforces mitotic repression of rRNA genes. At telophase, restoration of H2AQ104me is required for the activation of transcription. H2AQ104 methylation and chromatin dynamics are regulated by fibrillarin (FBL) and the NAD
Identifiants
pubmed: 31206100
doi: 10.1177/2516865719849090
pii: 10.1177_2516865719849090
pmc: PMC6537492
doi:
Types de publication
Journal Article
Comment
Langues
eng
Pagination
2516865719849090Commentaires et corrections
Type : CommentOn
Déclaration de conflit d'intérêts
Declaration of conflicting interests:The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
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