Zoologisches Institut, Universität Zürich, 8057 Zürich, Switzerland.
J Biol Chem. 2010 Dec 17;285(51):39623-36. doi: 10.1074/jbc.M110.140467. Epub 2010 Oct 11.
The Myc proto-oncoproteins are transcription factors that recognize numerous target genes through hexameric DNA sequences called E-boxes. The mechanism by which they then activate the expression of these targets is still under debate. Here, we use an RNAi screen in Drosophila S2 cells to identify Drosophila host cell factor (dHCF) as a novel co-factor for Myc that is functionally required for the activation of a Myc-dependent reporter construct. dHCF is also essential for the full activation of endogenous Myc target genes in S2 cells, and for the ability of Myc to promote growth in vivo. Myc and dHCF physically interact, and they colocalize on common target genes. Furthermore, down-regulation of dHCF-associated histone acetyltransferase and histone methyltransferase complexes in vivo interferes with the Myc biological activities. We therefore propose that dHCF recruits such chromatin-modifying complexes and thereby contributes to the expression of Myc targets and hence to the execution of Myc biological activities.
Myc 原癌蛋白是转录因子,通过称为 E 盒的六聚体 DNA 序列识别众多靶基因。它们激活这些靶基因的表达的机制仍存在争议。在这里,我们使用果蝇 S2 细胞中的 RNAi 筛选鉴定出果蝇宿主细胞因子 (dHCF) 作为 Myc 的一种新型共因子,它在激活依赖 Myc 的报告基因构建体方面是功能必需的。dHCF 对于 S2 细胞中内源性 Myc 靶基因的完全激活以及 Myc 在体内促进生长的能力也是必需的。Myc 和 dHCF 相互作用,并在共同的靶基因上共定位。此外,体内下调与 dHCF 相关的组蛋白乙酰转移酶和组蛋白甲基转移酶复合物会干扰 Myc 的生物学活性。因此,我们提出 dHCF 募集这种染色质修饰复合物,从而有助于 Myc 靶基因的表达,并执行 Myc 的生物学活性。