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在小鼠T细胞受体α基因和Dad1基因之间发现了依赖CTCF和不依赖CTCF的绝缘子。

Both CTCF-dependent and -independent insulators are found between the mouse T cell receptor alpha and Dad1 genes.

作者信息

Magdinier Frédérique, Yusufzai Timur M, Felsenfeld Gary

机构信息

Laboratory of Molecular Biology, NIDDK, National Institutes of Health, Bethesda, Maryland 20892-0504, USA.

出版信息

J Biol Chem. 2004 Jun 11;279(24):25381-9. doi: 10.1074/jbc.M403121200. Epub 2004 Apr 13.

Abstract

The T cell rearrangement of the T cell receptor (TCR) genes TCRalpha and delta is specifically regulated by a complex interplay between enhancer elements and chromatin structure. The alpha enhancer is active in T cells and drives TCRalpha recombination in collaboration with a locus control region-like element located downstream of the Calpha gene on mouse chromosome 14. Twelve kb further down-stream lies another gene, Dad1, with a program of expression different from that of TCRalpha. The approximately 6-kb locus control region element lying between them contains multiple regulatory sites with a variety of roles in regulating the two genes. Previous evidence has indicated that among these there are widely distributed regions with enhancer blocking (insulating) activity. We have shown in this report that one of these sites, not previously examined, strongly binds the insulator protein CCTC-binding factor (CTCF) in vitro and in vivo and can function in an enhancer blocking assay. However, other regions within the 6-kb element that also can block enhancers clearly do not harbor CTCF sites and thus must reflect the presence of a previously undetected and distinct vertebrate insulator activity.

摘要

T细胞受体(TCR)基因TCRα和δ的T细胞重排受到增强子元件与染色质结构之间复杂相互作用的特异性调控。α增强子在T细胞中具有活性,并与位于小鼠14号染色体上Calpha基因下游的一个类似基因座控制区的元件协同驱动TCRα重组。再往下游12 kb处是另一个基因Dad1,其表达模式与TCRα不同。位于它们之间的约6 kb基因座控制区元件包含多个调控位点,在调控这两个基因方面具有多种作用。先前的证据表明,其中存在广泛分布的具有增强子阻断(绝缘)活性的区域。我们在本报告中表明,这些位点之一(以前未进行过研究)在体外和体内都能与绝缘子蛋白CCTC结合因子(CTCF)强烈结合,并且在增强子阻断试验中发挥作用。然而,6 kb元件内其他同样能够阻断增强子的区域显然不含有CTCF位点,因此必定反映出存在一种以前未被检测到的独特的脊椎动物绝缘子活性。

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