PHF8

From WikiMD's medical encyclopedia

PHF8 (Plant Homeodomain Finger Protein 8) is a protein that in humans is encoded by the PHF8 gene. It is a histone lysine demethylase that is involved in the regulation of gene expression. Mutations in this gene have been associated with X-linked mental retardation and cleft lip/cleft palate.

Function

PHF8 is a histone demethylase that specifically demethylates 'Lys-9' (H3K9me) and 'Lys-27' (H3K27me) of histone H3, thereby playing a central role in histone code. It preferentially demethylates mono- and dimethylated H3 'Lys-9' and H3 'Lys-27', but has weak or no activity on trimethylated forms. Demethylation of Lys residue generates formaldehyde and succinate.

Clinical significance

Mutations in the PHF8 gene have been associated with X-linked mental retardation with cleft lip/cleft palate. The PHF8 protein may play a role in the regulation of transcription, and it interacts with genes that contain a specific DNA sequence. Mutations in the PHF8 gene disrupt the protein's ability to bind to DNA, which may affect the regulation of certain genes during development.

See also

References


External links

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