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Human BAHD1 promotes heterochromatic gene silencing.
Bierne H., Tham T. N., Batsche E., Dumay A., Leguillou M., Kernéis-Golsteyn S., Regnault B., Seeler J. S., Muchardt C., Feunteun J. et al
Proceedings of the National Academy of Sciences of the United States of America 106, 33 (2009) 13826-31 - http://hal-pasteur.archives-ouvertes.fr/pasteur-00411478
(19666599)
Human BAHD1 promotes heterochromatic gene silencing.
Hélène Bierne () 1, To Nam Tham1, Eric Batsche2, Anne Dumay3, Morwenna Leguillou3, Sophie Kernéis-Golsteyn4, Béatrice Regnault5, Jacob S. Seeler6, Christian Muchardt2, Jean Feunteun3, Pascale Cossart () 1
1 :  UIBC - Interactions Bactéries-Cellules
INSERM : U604 – Institut national de la recherche agronomique (INRA) – Institut Pasteur de Paris
25-28 rue du Docteur Roux, F-75724 Paris Cedex 15
France
2 :  Régulation Epigénétique
Institut Pasteur de Paris – CNRS : URA2578
25-28 rue du Docteur Roux 75724 Paris Cedex 15
France
3 :  GC - Génomes et cancer
CNRS : FRE2939 – Institut Gustave Roussy – Université Paris XI - Paris Sud
pavillon de recherche 1 39 Rue Camille Desmoulins 94805 VILLEJUIF CEDEX
France
4 :  Microscopie électronique (Plate-forme)
Institut Pasteur de Paris
25 rue du Docteur Roux, F-75724 Paris Cedex 15
France
5 :  Puces à ADN (Plate-Forme)
Institut Pasteur de Paris
25-28 rue du Docteur Roux 75724 Paris Cedex 15
France
6 :  Organisation Nucléaire et Oncogenèse
INSERM : U579 – Institut Pasteur de Paris
25-28 rue du Docteur Roux, F-75724 Paris Cedex 15
France
Gene silencing via heterochromatin formation plays a major role in cell differentiation and maintenance of homeostasis. Here we report the identification and characterization of a novel heterochromatinization factor in vertebrates, bromo adjacent homology domain-containing protein 1 (BAHD1). This nuclear protein interacts with HP1, MBD1, HDAC5, and several transcription factors. Through electron and immunofluorescence microscopy studies, we show that BAHD1 overexpression directs HP1 to specific nuclear sites and promotes the formation of large heterochromatic domains, which lack acetyl histone H4 and are enriched in H3 trimethylated at lysine 27 (H3K27me3). Furthermore, ectopically expressed BAHD1 colocalizes with the heterochromatic inactive X chromosome (Xi). The BAH domain is required for BAHD1 colocalization with H3K27me3, but not with the Xi chromosome. As highlighted by whole genome microarray analysis of BAHD1 knockdown cells, BAHD1 represses several proliferation and survival genes, in particular the insulin-like growth factor II gene (IGF2). When overexpressed, BAHD1 specifically binds the CpG-rich P3 promoter of IGF2, which increases MBD1 and HDAC5 targeting at this locus. This region contains DNA-binding sequences for the transcription factor SP1, with which BAHD1 coimmunoprecipitates. Collectively, these findings provide evidence that BAHD1 acts as a silencer by recruiting at specific promoters a set of proteins that coordinate heterochromatin assembly.
Sciences du Vivant/Biologie cellulaire
Anglais
0027-8424

Articles dans des revues avec comité de lecture
10.1073/pnas.0901259106
Proceedings of the National Academy of Sciences of the United States of America
internationale
18/08/2009
03/08/2009
106
33
13826-31