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Projekt Druckansicht

Charakterisierung eines 5-Formylcytosin Chromozentrums in Xenopus-Embryonen

Fachliche Zuordnung Entwicklungsbiologie
Förderung Förderung von 2017 bis 2021
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 354741800
 
Erstellungsjahr 2021

Zusammenfassung der Projektergebnisse

In active DNA demethylation, TET enzymes oxidize 5‐methylcytosine to 5‐hydroxymethylcytosine, 5‐formylcytosine (5fC), and 5‐carboxylcytosine as demethylation intermediates. An outstanding question is whether these oxidized cytosine derivatives have functional roles beyond being demethylation intermediates. We had discovered a 5fC nuclear chromocenter, which transiently forms during zygotic genome activation (ZGA) in Xenopus embryos. The aim of the DFG‐funded project was to characterize this 5fC chromocenter. During the funding period, we identified this chromocenter as the perinucleolar compartment, a structure localized at the periphery of the nucleolus, which is associated with transcription by RNA polymerase III (Pol III). By genomic profiling, 5fC is highly enriched on Pol III target genes and 5fC peaks correlate with active Pol III gene expression. Via manipulating Tet and Tdg enzymes, we find that 5fC is required as regulatory mark to promote Pol III and TFIIIC recruitment and activation of Pol III target genes. The results indicate an unexpected role of 5fC as epigenetic regulator during Pol III gene expression in early vertebrate development.

Projektbezogene Publikationen (Auswahl)

 
 

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