Histone deacetylase 3 is required for centromeric H3K4 deacetylation and sister chromatid cohesion
- Grégory Eot-Houllier1,2,3,5,
- Géraldine Fulcrand1,2,3,6,
- Yoshinori Watanabe4,
- Laura Magnaghi-Jaulin1,2,3,6, and
- Christian Jaulin1,2,3,6,7
- 1 INSERM, U860, Montpellier, F-34298 France;
- 2 CRLC Val d’Aurelle-Paul Lamarque, Montpellier, F-34298 France;
- 3 Université Montpellier1, Montpellier, F-34298 France;
- 4 Laboratory of Chromosome Dynamics, Institute of Molecular and Cellular Biosciences, University of Tokyo, Yayoi, Tokyo 113-0032, Japan.
Abstract
We describe here the role of histone deacetylase 3 (HDAC3) in sister chromatid cohesion and the deacetylation of histone H3 Lys 4 (H3K4) at the centromere. HDAC3 knockdown induced spindle assembly checkpoint activation and sister chromatid dissociation. The depletion of Polo-like kinase 1 (Plk1) or Aurora B restored cohesion in HDAC3-depleted cells. HDAC3 was also required for Shugoshin localization at centromeres. Finally, we show that HDAC3 depletion results in the acetylation of centromeric H3K4, correlated with a loss of dimethylation at the same position. These findings provide a functional link between sister chromatid cohesion and the mitotic “histone code”.
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Footnotes
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↵5 Present addresses: Groupe Microtubules et Cycle Cellulaire, Institut de Génétique Humaine, CNRS UPR 1142, rue de la cardonille, 34396 Montpellier cedex 5, France;
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↵6 CNRS UMR 6061, Institut de Génétique et Développement, Université de Rennes I, IFR 140, 2 Avenue du Pr Léon Bernard, 35043 Rennes cedex, France.
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↵7 Corresponding author.
↵7 E-MAIL christian.jaulin@univ-rennes1.fr; FAX 33-2-23-23-44-78.
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Supplemental material is available at http://www.genesdev.org.
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Article is online at http://www.genesdev.org/cgi/doi/10.1101/gad.484108.
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- Received April 21, 2008.
- Accepted August 11, 2008.
- Copyright © 2008, Cold Spring Harbor Laboratory Press