Kirmizis Antonis, Bartley Stephanie M, Kuzmichev Andrei, Margueron Raphael, Reinberg Danny, Green Roland, Farnham Peggy J
McArdle Laboratory for Cancer Research, University of Wisconsin Medical School, Madison, Wisconsin 53706, USA.
Genes Dev. 2004 Jul 1;18(13):1592-605. doi: 10.1101/gad.1200204.
Polycomb group (PcG) complexes 2 and 3 are involved in transcriptional silencing. These complexes contain a histone lysine methyltransferase (HKMT) activity that targets different lysine residues on histones H1 or H3 in vitro. However, it is not known if these histones are methylation targets in vivo because the human PRC2/3 complexes have not been studied in the context of a natural promoter because of the lack of known target genes. Here we report the use of RNA expression arrays and CpG-island DNA arrays to identify and characterize human PRC2/3 target genes. Using oligonucleotide arrays, we first identified a cohort of genes whose expression changes upon siRNA-mediated removal of Suz12, a core component of PRC2/3, from colon cancer cells. To determine which of the putative target genes are directly bound by Suz12 and to precisely map the binding of Suz12 to those promoters, we combined a high-resolution chromatin immunoprecipitation (ChIP) analysis with custom oligonucleotide promoter arrays. We next identified additional putative Suz12 target genes by using ChIP coupled to CpG-island microarrays. We showed that HKMT-Ezh2 and Eed, two other components of the PRC2/3 complexes, colocalize to the target promoters with Suz12. Importantly, recruitment of Suz12, Ezh2 and Eed to target promoters coincides with methylation of histone H3 on Lys 27.
多梳蛋白家族(PcG)复合物2和3参与转录沉默。这些复合物含有一种组蛋白赖氨酸甲基转移酶(HKMT)活性,该活性在体外靶向组蛋白H1或H3上的不同赖氨酸残基。然而,由于缺乏已知的靶基因,尚未在天然启动子的背景下研究人PRC2/3复合物,因此尚不清楚这些组蛋白在体内是否为甲基化靶点。在此,我们报告使用RNA表达阵列和CpG岛DNA阵列来鉴定和表征人PRC2/3靶基因。使用寡核苷酸阵列,我们首先鉴定了一组基因,其表达在通过小干扰RNA(siRNA)介导从结肠癌细胞中去除PRC2/3的核心成分Suz12后发生变化。为了确定哪些推定的靶基因被Suz12直接结合,并精确绘制Suz12与那些启动子的结合图谱,我们将高分辨率染色质免疫沉淀(ChIP)分析与定制的寡核苷酸启动子阵列相结合。接下来,我们通过使用与CpG岛微阵列偶联的ChIP鉴定了其他推定的Suz12靶基因。我们表明,PRC2/3复合物的另外两个成分HKMT-Ezh2和Eed与Suz12共定位于靶启动子。重要的是,Suz12、Ezh2和Eed募集到靶启动子与组蛋白H3赖氨酸27位的甲基化同时发生。