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Histones can be reversibly acetylated on several lysine residues.
Regulation of transcription is caused in part by this
mechanism. Histone deacetylases catalyse the removal
of the acetyl group. Histone deacetylases, acetoin utilization proteins and acetylpolyamine amidohydrolases are all members of this ancient protein superfamily [PMID:9278492].
HDAs function in multi-subunit complexes, reversing the acetylation of
histones by histone acetyltransferases [PMID:10322454, PMID:10072350], and are also believed to deacetylate general transcription factors such as TFIIF and sequence-specific transcription factors such as p53 [PMID:10322454]. Thus, HDAs contribute to the regulation of transcription, in particular transcriptional repression [PMID:10072350]. At N-terminal tails of histones, removal of the acetyl group from the epsilon-amino group of a lysine side chain will restore its positivecharge, which may stabilise the histone-DNA interaction and prevent activating transcription factors binding to promoter elements [PMID:9278492]. HDAs play important roles in the cell cycle and differentiation, and their
deregulation can contribute to the development of cancer [PMID:10072350, PMID:10322142].
HDAs function in multi-subunit complexes, reversing the acetylation of
histones by histone acetyltransferases [PMID:10322454, PMID:10072350], and are also believed to
deacetylate general transcription factors such as TFIIF and sequence-
specific transcription factors such as p53 [PMID:10322454]. Thus, HDAs contribute to
the regulation of transcription, in particular transcriptional repression. At N-terminal tails of histones, removal of the acetyl group from
the epsilon-amino group of a lysine side chain will restore its positive
charge, which may stabilise the histone-DNA interaction and prevent
activating transcription factors binding to promoter elements [PMID:9278492]. HDAs
play important roles in the cell cycle and differentiation, and their
deregulation can contribute to the development of cancer [PMID:10072350, PMID:10322142].
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