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人类辅助性T细胞2型(T(H)2)中白细胞介素4(IL-4)基因的染色质结构与DNA甲基化

Chromatin structure and DNA methylation of the IL-4 gene in human T(H)2 cells.

作者信息

Santangelo Samantha, Cousins David J, Winkelmann Nicole, Triantaphyllopoulos Kostas, Staynov Dontcho Z

机构信息

Santangelo Consulting Pty Ltd., Singapore, Singapore.

出版信息

Chromosome Res. 2009;17(4):485-96. doi: 10.1007/s10577-009-9040-3. Epub 2009 Jun 12.

Abstract

Human T(H)2 cell differentiation results in the selective demethylation of several specific CpG dinucleotides in the IL-4 and IL-13 genes, which are expressed in activated T(H)2, but not T(H)1, cells. This demethylation is accompanied by the appearance of six DNase I hypersensitive sites within 1.4 kb at the 5'-end of the IL-4 gene. Micrococcal nuclease (MNase) digestion revealed that in both T(H)1 and T(H)2 cells nine nucleosomes with a repeat length of 201 bp are identically positioned around the 5'-end of the IL-4 gene. However, only in T(H)2 cells are six out of the eight intervening linkers exposed to DNase I. This suggests that a major perturbation of the higher-order chromatin structure occurs above the level of the nucleosome in vivo. It is observed in cells that are poised for expression but which are not actively expressing the gene (i.e. resting T(H)2 cells). Notably, all the demethylated CpGs in T(H)2 cells are found in DNA that is accessible to DNase I. This may suggest that the opening of the chromatin structure allows binding of specific trans-acting factors that prevent de novo methylation.

摘要

人类辅助性T细胞2(T(H)2)分化导致白细胞介素4(IL-4)和白细胞介素13(IL-13)基因中几个特定的CpG二核苷酸选择性去甲基化,这些基因在活化的T(H)2细胞而非T(H)1细胞中表达。这种去甲基化伴随着IL-4基因5'端1.4 kb范围内出现六个脱氧核糖核酸酶I(DNase I)高敏位点。微球菌核酸酶(MNase)消化显示,在T(H)1和T(H)2细胞中,九个重复长度为201 bp的核小体围绕IL-4基因5'端呈相同定位。然而,只有在T(H)2细胞中,八个间隔连接区中的六个对DNase I敏感。这表明在体内,高阶染色质结构在核小体水平之上发生了重大扰动。在准备表达但未积极表达该基因的细胞(即静息T(H)2细胞)中观察到了这种情况。值得注意的是,T(H)2细胞中所有去甲基化的CpG都存在于对DNase I可及的DNA中。这可能表明染色质结构的开放允许特定反式作用因子结合,从而防止从头甲基化。

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