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HIRA and Daxx constitute two independent histone H3.3-containing predeposition complexes.
- Source :
-
Cold Spring Harbor symposia on quantitative biology [Cold Spring Harb Symp Quant Biol] 2010; Vol. 75, pp. 27-34. Date of Electronic Publication: 2010 Nov 03. - Publication Year :
- 2010
-
Abstract
- Histone H3.3 is a universal replacement histone in metazoans that has been implicated in diverse processes ranging from gene activation to heterochromatin silencing. Here, we show that, before deposition, H3.3 exists in two biochemically distinct complexes, associated with either Daxx or HIRA, Ubinuclein-1, and Cabin-1. Although the HIRA complex is evolutionarily conserved in yeast, Daxx is a novel histone chaperone unique to metazoans. Deletion of HIRA in mouse embryonic stem cells impairs the HIRA complex integrity but does not abolish Daxx association with H3.3/H4. Similarly, HIRA interacts with H3.3/H4 in the absence of Daxx. We hypothesize that these two H3.3 chaperone systems provide separate pools of H3/H4 units for incorporation at distinct sites within the genome. We provide evidence that the association of histone H3.3 with distinct assembly systems allows it to acquire unique posttranslational modifications before deposition that might affect its role after incorporation into chromatin.
- Subjects :
- Amino Acid Motifs
Amino Acid Sequence
Animals
Chromatin Assembly and Disassembly
Co-Repressor Proteins
HeLa Cells
Histones chemistry
Humans
Mice
Models, Biological
Molecular Chaperones
Molecular Sequence Data
Protein Binding
Protein Processing, Post-Translational
Signal Transduction
Carrier Proteins metabolism
Cell Cycle Proteins metabolism
Histone Chaperones metabolism
Histones metabolism
Intracellular Signaling Peptides and Proteins metabolism
Multiprotein Complexes metabolism
Nuclear Proteins metabolism
Transcription Factors metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1943-4456
- Volume :
- 75
- Database :
- MEDLINE
- Journal :
- Cold Spring Harbor symposia on quantitative biology
- Publication Type :
- Academic Journal
- Accession number :
- 21047901
- Full Text :
- https://doi.org/10.1101/sqb.2010.75.008