Vassen Lothar, Fiolka Katharina, Möröy Tarik
Institut für Zellbiologie (Tumorforschung), IFZ, Universitätsklinikum Essen, Essen, Germany.
EMBO J. 2006 Jun 7;25(11):2409-19. doi: 10.1038/sj.emboj.7601124. Epub 2006 May 11.
Gfi1b is a 37 kDa nuclear protein with six C2H2 zinc-finger domains that can silence transcription upon binding to specific target gene promoters. Here we show by using a chromatin immunoprecipitation and cloning protocol that Gfi1b also binds to gamma-satellite sequences that mainly occur in pericentric heterochromatin. Immuno-FISH experiments demonstrated that Gfi1b is localized at foci of pericentric heterochromatin identified by DAPI staining. Elevated levels of Gfi1b correlated with increased histone H3 lysine 9 dimethylation at sites neighboring gamma-satellite sequences but also at Gfi1b target gene promoters. In Gfi1b-deficient cells, however, a decrease of histone H3 lysine 9 trimethylation and a loss of heterochromatic structures was observed. Strikingly, we found that Gfi1b binds to both SUV39H1 and G9A histone methyl transferases, which provides a direct link between histone methylation and Gfi1b at heterochromatic and euchromatic sites. We propose that Gfi1b functions in heterochromatin formation and silencing of euchromatic transcription by recruiting histone methyl transferases to either gamma-satellite sequences or specific target gene promoters.
Gfi1b是一种37 kDa的核蛋白,具有六个C2H2锌指结构域,可在与特定靶基因启动子结合时使转录沉默。在这里,我们通过使用染色质免疫沉淀和克隆方案表明,Gfi1b还与主要出现在着丝粒周围异染色质中的γ-卫星序列结合。免疫荧光原位杂交实验表明,Gfi1b定位于通过DAPI染色鉴定的着丝粒周围异染色质的位点。Gfi1b水平升高与γ-卫星序列相邻位点以及Gfi1b靶基因启动子处组蛋白H3赖氨酸9二甲基化增加相关。然而,在Gfi1b缺陷细胞中,观察到组蛋白H3赖氨酸9三甲基化减少和异染色质结构丧失。引人注目的是,我们发现Gfi1b与SUV39H1和G9A组蛋白甲基转移酶都结合,这在异染色质和常染色质位点的组蛋白甲基化与Gfi1b之间建立了直接联系。我们提出,Gfi1b通过将组蛋白甲基转移酶募集到γ-卫星序列或特定靶基因启动子来参与异染色质形成和常染色质转录沉默。