Firestein R, Cui X, Huie P, Cleary M L
Department of Pathology, Stanford University Medical Center, CA 94305, USA.
Mol Cell Biol. 2000 Jul;20(13):4900-9. doi: 10.1128/MCB.20.13.4900-4909.2000.
Mammalian SET domain-containing proteins define a distinctive class of chromatin-associated factors that are targets for growth control signals and oncogenic activation. SUV39H1, a mammalian ortholog of Drosophila Su(var)3-9, contains both SET and chromo domains, signature motifs for proteins that contribute to epigenetic control of gene expression through effects on the regional organization of chromatin structure. In this report we demonstrate that SUV39H1 represses transcription in a transient transcriptional assay when tethered to DNA through the GAL4 DNA binding domain. Under these conditions, SUV39H1 displays features of a long-range repressor capable of acting over several kilobases to silence basal promoters. A possible role in chromatin-mediated gene silencing is supported by the localization of exogenously expressed SUV39H1 to nuclear bodies with morphologic features suggestive of heterochromatin in interphase cells. In addition, we show that SUV39H1 is phosphorylated specifically at the G(1)/S cell cycle transition and when forcibly expressed suppresses cell growth. Growth suppression as well as the ability of SUV39H1 to form nuclear bodies and silence transcription are antagonized by the oncogenic antiphosphatase Sbf1 that when hyperexpressed interacts with the SET domain and stabilizes the phosphorylated form of SUV39H1. These studies suggest a phosphorylation-dependent mechanism for regulating the chromatin organizing activity of a mammalian su(var) protein and implicate the SET domain as a gatekeeper motif that integrates upstream signaling pathways to epigenetic regulation and growth control.
含哺乳动物SET结构域的蛋白质定义了一类独特的与染色质相关的因子,它们是生长控制信号和致癌激活的靶点。SUV39H1是果蝇Su(var)3-9的哺乳动物同源物,它同时包含SET和染色质结构域,这是通过影响染色质结构的区域组织来促进基因表达表观遗传控制的蛋白质的特征基序。在本报告中,我们证明,当通过GAL4 DNA结合结构域与DNA相连时,SUV39H1在瞬时转录分析中会抑制转录。在这些条件下,SUV39H1表现出一种长程阻遏物的特征,能够作用于几千个碱基以沉默基础启动子。外源性表达的SUV39H1定位于具有间期细胞中异染色质形态特征的核体,这支持了其在染色质介导的基因沉默中的可能作用。此外,我们表明SUV39H1在G(1)/S细胞周期转换时被特异性磷酸化,并且当被强制表达时会抑制细胞生长。致癌性抗磷酸酶Sbf1会拮抗生长抑制以及SUV39H1形成核体和沉默转录的能力,Sbf1过表达时会与SET结构域相互作用并稳定SUV39H1的磷酸化形式。这些研究提示了一种磷酸化依赖的机制来调节哺乳动物su(var)蛋白的染色质组织活性,并表明SET结构域是一个守门基序,它将上游信号通路整合到表观遗传调控和生长控制中。