Structure of the histone chaperone ASF1 bound to the histone H3 C-terminal helix and functional insights.
Asf1 is a histone chaperone that favors histone H3/H4 assembly and disassembly. We solved the structure of the conserved domain of human ASF1A in complex with the C-terminal helix of histone H3 using nuclear magnetic resonance spectroscopy. This structure is fully compatible with an association of ASF1 with the heterodimeric ... form of histones H3/H4. In our model, ASF1 substitutes for the second H3/H4 heterodimer that is normally found in heterotetrameric H3/H4 complexes. This result constitutes an essential step in the fundamental understanding of the mechanisms of nucleosome assembly by histone chaperones. Point mutations that perturb the Asf1/histone interface were designed from the structure. The decreased binding affinity of the Asf1-H3/H4 complex correlates with decreased levels of H3-K56 acetylation and phenotypic defects in vivo.
Mesh Terms:
Acetylation, Cell Cycle Proteins, Cells, Cultured, Dimerization, Histones, Humans, Magnetic Resonance Spectroscopy, Molecular Chaperones, Point Mutation, Protein Structure, Secondary, Protein Structure, Tertiary
Acetylation, Cell Cycle Proteins, Cells, Cultured, Dimerization, Histones, Humans, Magnetic Resonance Spectroscopy, Molecular Chaperones, Point Mutation, Protein Structure, Secondary, Protein Structure, Tertiary
Structure
Date: Feb. 01, 2007
PubMed ID: 17292837
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