Institut für Genetik, Justus-Liebig-Universität Giessen, Heinrich-Buff-Ring 58-62, 35392 Giessen, Germany.
Development. 2012 Mar;139(6):1045-57. doi: 10.1242/dev.065268.
The genome of higher eukaryotes exhibits a patchwork of inactive and active genes. The nuclear protein CCCTC-binding factor (CTCF) when bound to insulator sequences can prevent undesirable crosstalk between active and inactive genomic regions, and it can also shield particular genes from enhancer function, a role that has many applications in development. Exciting recent work has demonstrated roles for CTCF in, for example, embryonic, neuronal and haematopoietic development. Here, we discuss the underlying mechanisms of developmentally regulated CTCF-dependent transcription in relation to model genes, and highlight genome-wide results indicating that CTCF might play a master role in regulating both activating and repressive transcription events at sites throughout the genome.
高等真核生物的基因组表现出失活基因和活跃基因的拼凑。当核蛋白 CCCTC 结合因子 (CTCF) 结合到绝缘子序列时,可以防止活跃和失活基因组区域之间的不良串扰,它还可以保护特定基因免受增强子功能的影响,这种作用在发育中有许多应用。最近令人兴奋的工作表明,CTCF 在胚胎、神经元和造血发育等方面发挥作用。在这里,我们讨论了与模型基因相关的发育调控的 CTCF 依赖性转录的潜在机制,并强调了全基因组的结果表明,CTCF 可能在调节整个基因组中活跃和抑制转录事件方面发挥主要作用。