Fungi - Candida albicans - Research News, Data, Publications & Aproaches - ERG11 Mutations - Telomeres - Sub-Telomeric Structures - Chromatin Landscape - Nuclear Biology & Nuclear Chemistry Aproaches - Redox–Chromatin Coupling - Non-Elaborate Posts - Post 3
Oxidative stress, generated either by host immune defenses or azole exposure, penetrates the nuclear microenvironment as both a damaging and regulatory signal. Reactive oxygen species (ROS) oxidize cysteine residues within histone-modifying enzymes, transiently inhibiting deacetylases while activating specific demethylases such as JmjC-domain proteins, which require Fe(II) and α-ketoglutarate as cofactors. This redox perturbation leads to histone H3K9 demethylation, chromatin relaxation, and upregulation of ERG11. Hence, the nucleus acts as a redox sensor: chemical electrons determine the transcriptional output, and the genomic defense system responds not with simple repair but with transcriptional adaptation.
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