Alp13, an MRG family
protein, is a component of fission yeast Clr6 histone deacetylase required
for genomic integrity
Nakayama J, Xiao G, Noma K, Malikzay A, Bjerling P, Ekwall K, Kobayashi
R and Grewal S I
Embo J 22(11):2776-87 (2003)
SUMMARY
The post-translational modifications of histones are key to the modulation
of chromatin structure. Distinct patterns of modifications established
by histone-modifying enzymes control diverse chromosomal processes. Here,
we report the purification and molecular characterization of the fission
yeast Clr6 histone deacetyl ase involved in higher order chromatin assembly.
We show that a chromodomain protein Alp13, which belongs to the conserved
MRG protein family linked to cellular senescence in humans, is associated
with Clr6. In addition, Clr6 interacts with homologs of the mammalian
transcriptional co-repressors Sin3, Pst1 and Pst2, and a WD40 repeat-containing
protein, Prw1. Alp13, Pst2 and Prw1 form a stable complex with Clr6 in
the nucleus. Deletion of any of these factors causes progressive loss
of viability and sensitivity to DNA-damaging agents, and impairs condensation/resolution
of chromosomes during mitosis. This is accompanied by hyperacetylation
of histones and a reduction in histone H3 Ser10 phosphorylation, which
correlates with chromosome condensation during mitosis. These results
link the MRG family protein Alp13 to histone deacetylation, and suggest
that Clr6 and its associated factors are essential for fundamental chromosomal
events.
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