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Interaction with members of the heterochromatin protein 1 (HP1) family and histone deacetylation are differentially involved in transcriptional silencing by members of the TIF1 family
Author(s) -
Nielsen Anders L.,
Ortiz José A.,
You Jun,
OuladAbdelghani Mustapha,
Khechumian Ruben,
Gansmuller Anne,
Chambon Pierre,
Losson Régine
Publication year - 1999
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/18.22.6385
Subject(s) - heterochromatin protein 1 , euchromatin , biology , heterochromatin , trichostatin a , sap30 , histone , gene silencing , genetics , histone methyltransferase , histone deacetylase , microbiology and biotechnology , chromatin , gene
Mammalian TIF1α and TIF1β (KAP‐1/KRIP‐1) are related transcriptional intermediary factors that possess intrinsic silencing activity. TIF1α is believed to be a euchromatic target for liganded nuclear receptors, while TIF1β may serve as a co‐repressor for the large family of KRAB domain‐containing zinc finger proteins. Here, we report an association of TIF1β with both heterochromatin and euchromatin in interphase nuclei. Co‐immunoprecipitation of nuclear extracts shows that endogenous TIF1β, but not TIF1α, is associated with members of the heterochromatin protein 1 (HP1) family. However, in vitro , both TIF1α and TIF1β interact with and phosphorylate the HP1 proteins. This interaction involves a conserved amino acid motif, which is critical for the silencing activity of TIF1β but not TIF1α. We further show that trichostatin A, an inhibitor of histone deacetylases, can interfere with both TIF1 and HP1 silencing. The silencing activity of TIF1α appears to result chiefly from histone deacetylation, whereas that of TIF1β may be mediated via both HP1 binding and histone deacetylation.