Storre Jörg, Schäfer Andrea, Reichert Nina, Barbero José Luis, Hauser Stefanie, Eilers Martin, Gaubatz Stefan
Institute for Molecular Biology and Tumor Research (IMT), Philipps-University Marburg, 35037 Marburg, Germany.
J Biol Chem. 2005 Dec 16;280(50):41380-6. doi: 10.1074/jbc.M506797200. Epub 2005 Oct 19.
E2F6, a member of the E2F-family of transcription factors, is a retinoblastoma protein-independent transcriptional repressor. E2F6 associates with polycomb group (Pc-G) multiprotein complexes that contain histone H3 methyltransferases, suggesting that E2F6 represses genes by covalent histone modification. However, genes that are repressed by E2F6 via a mechanism that involves histone H3 methylation have not been identified. Using cDNA microarray experiments comparing wild-type and E2f6-/- mouse embryonic fibroblasts, we now found that E2F6 is required to silence the meiosis-specific genes SMC1beta and STAG3 in somatic cells. Re-expression of E2F6 in E2f6-/- cells was sufficient to restore their repression. E2F6 binds in vivo to the promoters of these genes through a conserved binding site. Transcriptional repression of SMC1beta and STAG3 by E2F6 involves multiple mechanisms, including methylation of histone H3 on lysine 9 and lysine 27. Our findings suggest a molecular mechanism for the stable transcriptional silencing of meiotic genes in somatic cells by E2F6.
E2F6是转录因子E2F家族的成员之一,是一种不依赖视网膜母细胞瘤蛋白的转录抑制因子。E2F6与包含组蛋白H3甲基转移酶的多梳蛋白复合体(Pc-G)相关联,这表明E2F6通过共价组蛋白修饰来抑制基因。然而,尚未鉴定出E2F6通过涉及组蛋白H3甲基化的机制所抑制的基因。通过使用cDNA微阵列实验比较野生型和E2f6基因敲除小鼠胚胎成纤维细胞,我们现在发现E2F6是体细胞中沉默减数分裂特异性基因SMC1β和STAG3所必需的。在E2f6基因敲除细胞中重新表达E2F6足以恢复对这些基因的抑制。E2F6在体内通过一个保守的结合位点与这些基因的启动子结合。E2F6对SMC1β和STAG3的转录抑制涉及多种机制,包括组蛋白H3赖氨酸9和赖氨酸27的甲基化。我们的研究结果揭示了E2F6在体细胞中对减数分裂基因进行稳定转录沉默的分子机制。