Histone deacetylase 3 is required for centromeric H3K4 deacetylation and sister chromatid cohesion

Archive ouverte

Eot-Houllier, Grégory | Fulcrand, Géraldine | Watanabe, Yoshinori | Magnaghi-Jaulin, Laura | Jaulin, Christian

Edité par CCSD ; Cold Spring Harbor Laboratory Press -

International audience. 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”.

Consulter en ligne

Suggestions

Du même auteur

Histone Deacetylase Inhibitors Induce Premature Sister Chromatid Separation and Override the Mitotic Spindle Assembly Checkpoint

Archive ouverte | Magnaghi-Jaulin, Laura | CCSD

International audience. Abstract Histone deacetylase inhibitors (HDACI) are powerful antiproliferative drugs, and are currently undergoing clinical trials as antitumor agents. It would be valuable for both cancer th...

Histone deacetylase inhibitors and genomic instability.

Archive ouverte | Eot-Houllier, Grégory | CCSD

International audience. Histone deacetylase inhibitors (HDACIs) are a promising new class of anticancer drugs. However, their mechanism of action has not been fully elucidated. Most studies have investigated the eff...

Histone deacetylase 3 is required for centromeric H3K4 deacetylation and sister chromatid cohesion.

Archive ouverte | Eot-Houllier, G. | CCSD

International audience

Chargement des enrichissements...