Kim Jeong Do, Hinz Angela K, Bergmann Anne, Huang Jennifer M, Ovcharenko Ivan, Stubbs Lisa, Kim Joomyeong
Department of Biological Sciences, Center for BioModular Multi-Scale Systems, Louisiana State University, Baton Rouge, Louisiana 70803, USA.
Genome Res. 2006 Jul;16(7):901-11. doi: 10.1101/gr.5091406. Epub 2006 Jun 7.
Mammalian genomic imprinting is regulated by imprinting control regions (ICRs) that are usually associated with tandem arrays of transcription factor binding sites. In this study, the sequence features derived from a tandem array of YY1 binding sites of Peg3-DMR (differentially methylated region) led us to identify three additional clustered YY1 binding sites, which are also localized within the DMRs of Xist, Tsix, and Nespas. These regions have been shown to play a critical role as ICRs for the regulation of surrounding genes. These ICRs have maintained a tandem array of YY1 binding sites during mammalian evolution. The in vivo binding of YY1 to these regions is allele specific and only to the unmethylated active alleles. Promoter/enhancer assays suggest that a tandem array of YY1 binding sites function as a potential orientation-dependent enhancer. Insulator assays revealed that the enhancer-blocking activity is detected only in the YY1 binding sites of Peg3-DMR but not in the YY1 binding sites of other DMRs. Overall, our identification of three additional clustered YY1 binding sites in imprinted domains suggests a significant role for YY1 in mammalian genomic imprinting.
哺乳动物基因组印记由印记控制区域(ICR)调控,这些区域通常与转录因子结合位点的串联阵列相关。在本研究中,源自Peg3 - DMR(差异甲基化区域)的YY1结合位点串联阵列的序列特征引导我们鉴定出另外三个成簇的YY1结合位点,它们也位于Xist、Tsix和Nespas的DMR内。这些区域已被证明作为ICR对周围基因的调控起着关键作用。在哺乳动物进化过程中,这些ICR维持了YY1结合位点的串联阵列。YY1在体内与这些区域的结合具有等位基因特异性,且仅与未甲基化的活性等位基因结合。启动子/增强子分析表明,YY1结合位点的串联阵列作为一种潜在的方向依赖性增强子发挥作用。绝缘子分析显示,仅在Peg3 - DMR的YY1结合位点检测到增强子阻断活性,而在其他DMR的YY1结合位点未检测到。总体而言,我们在印记区域鉴定出另外三个成簇的YY1结合位点,表明YY1在哺乳动物基因组印记中发挥重要作用。