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NF-E2在体内通过β-珠蛋白基因座控制区的5'超敏位点2重塑染色质结构和激活ε-珠蛋白基因转录中的关键作用。

Essential role of NF-E2 in remodeling of chromatin structure and transcriptional activation of the epsilon-globin gene in vivo by 5' hypersensitive site 2 of the beta-globin locus control region.

作者信息

Gong Q H, McDowell J C, Dean A

机构信息

Laboratory of Cellular and Developmental Biology, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892-2715, USA.

出版信息

Mol Cell Biol. 1996 Nov;16(11):6055-64. doi: 10.1128/MCB.16.11.6055.

Abstract

Much of our understanding of the process by which enhancers activate transcription has been gained from transient-transfection studies in which the DNA is not assembled with histones and other chromatin proteins as it is in the cell nucleus. To study the activation of a mammalian gene in a natural chromatin context in vivo, we constructed a minichromosome containing the human epsilon-globin gene and portions of the beta-globin locus control region (LCR). The minichromosomes replicate and are maintained at stable copy number in human erythroid cells. Expression of the minichromosomal epsilon-globin gene requires the presence of beta-globin LCR elements in cis, as is the case for the chromosomal gene. We determined the chromatin structure of the epsilon-globin gene in both the active and inactive states. The transcriptionally inactive locus is covered by an array of positioned nucleosomes extending over 1,400 bp. In minichromosomes with a (mu)LCR or DNase I-hypersensitive site 2 (HS2) which actively transcribe the epsilon-globin gene, the nucleosome at the promoter is altered or disrupted while positioning of nucleosomes in the rest of the locus is retained. All or virtually all minichromosomes are simultaneously hypersensitive to DNase I both at the promoter and at HS2. Transcriptional activation and promoter remodeling, as well as formation of the HS2 structure itself, depended on the presence of the NF-E2 binding motif in HS2. The nucleosome at the promoter which is altered upon activation is positioned over the transcriptional elements of the epsilon-globin gene, i.e., the TATA, CCAAT, and CACCC elements, and the GATA-1 site at -165. The simple availability of erythroid transcription factors that recognize these motifs is insufficient to allow expression. As in the chromosomal globin locus, regulation also occurs at the level of chromatin structure. These observations are consistent with the idea that one role of the beta-globin LCR is to maintain promoters free of nucleosomes. The restricted structural change observed upon transcriptional activation may indicate that the LCR need only make a specific contact with the proximal gene promoter to activate transcription.

摘要

我们对增强子激活转录过程的许多理解都来自瞬时转染研究,在这些研究中,DNA不像在细胞核中那样与组蛋白和其他染色质蛋白组装在一起。为了在体内自然染色质环境中研究哺乳动物基因的激活,我们构建了一个包含人ε-珠蛋白基因和部分β-珠蛋白基因座控制区(LCR)的微型染色体。这些微型染色体在人类红细胞中复制并以稳定的拷贝数维持。微型染色体上ε-珠蛋白基因的表达需要顺式存在β-珠蛋白LCR元件,这与染色体基因的情况相同。我们确定了ε-珠蛋白基因在活跃和非活跃状态下的染色质结构。转录非活跃位点被一系列定位核小体覆盖,延伸超过1400 bp。在含有(μ)LCR或DNase I超敏位点2(HS2)并积极转录ε-珠蛋白基因的微型染色体中,启动子处的核小体发生改变或破坏,而基因座其余部分的核小体定位得以保留。所有或几乎所有微型染色体在启动子和HS2处同时对DNase I超敏。转录激活和启动子重塑,以及HS2结构本身的形成,取决于HS2中NF-E2结合基序的存在。激活时发生改变的启动子处的核小体位于ε-珠蛋白基因的转录元件上,即TATA、CCAAT和CACCC元件,以及-165处的GATA-1位点。识别这些基序的红系转录因子的简单可用性不足以允许表达。与染色体珠蛋白基因座一样,调控也发生在染色质结构水平。这些观察结果与β-珠蛋白LCR的一个作用是使启动子不含核小体的观点一致。转录激活时观察到的有限结构变化可能表明,LCR只需与近端基因启动子进行特定接触即可激活转录。

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