Wallace Julie A, Felsenfeld Gary
Laboratory of Molecular Biology, NIDDK, National Institutes of Health, Bethesda, MD 20892-0540, United States.
Curr Opin Genet Dev. 2007 Oct;17(5):400-7. doi: 10.1016/j.gde.2007.08.005. Epub 2007 Oct 24.
When placed between an enhancer and promoter, certain DNA sequence elements inhibit enhancer-stimulated gene expression. The best characterized of these enhancer-blocking insulators, gypsy in Drosophila and the CTCF-binding element in vertebrates and flies, stabilize contacts between distant genomic regulatory sites leading to the formation of loop domains. Current results show that CTCF mediates long-range contacts in the mouse beta-globin locus and at the Igf2/H19-imprinted locus. Recently described active chromatin hubs and transcription factories also involve long-range interactions; it is likely that CTCF interferes with their formation when acting as an insulator. The properties of CTCF, and its newly described genomic distribution, suggest that it may play an important role in large-scale nuclear architecture, perhaps mediated by the co-factors with which it interacts in vivo.
当置于增强子和启动子之间时,某些DNA序列元件会抑制增强子刺激的基因表达。这些增强子阻断绝缘子中最具特征的,果蝇中的gypsy以及脊椎动物和果蝇中的CTCF结合元件,稳定了远距离基因组调控位点之间的接触,导致环结构域的形成。目前的结果表明,CTCF介导小鼠β-珠蛋白基因座和Igf2/H19印记基因座中的长程接触。最近描述的活性染色质枢纽和转录工厂也涉及长程相互作用;当作为绝缘子起作用时,CTCF可能会干扰它们的形成。CTCF的特性及其新描述的基因组分布表明,它可能在大规模核结构中发挥重要作用,也许是由其在体内相互作用的辅助因子介导的。