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Zinc finger MYND-type containing 8 (ZMYND8) is a human chromatin-associated protein characterized by a MYND-type zinc finger, a bromodomain, and a plant homeodomain (PHD) finger. It acts as an epigenetic "reader," recognizing specific acetylated lysine residues on histone tails—particularly H3K14ac and H4K16ac—thereby regulating transcription, genome stability, and DNA double-strand break repair. ZMYND8 interacts with DNA repair machinery at damaged chromatin and collaborates with other zinc finger proteins and PARP1 to promote homologous recombination. Reduced or epigenetically silenced expression of ZMYND8 has been linked to a worse prognosis and increased genomic instability in cancers, positioning it as a potential tumor suppressor and biomarker in oncology[1][6][8][10].
Chromatin reader-binding to acetylated histone lysine residues, regulating gene expression and DNA damage response; Protein–protein interaction via MYND domain, recruiting other DNA repair or chromatin-associated factors
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