[DNA bend sites in the promoter region of the human estrogen receptor alpha gene].

K Kuwabara, Y Sakuma
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引用次数: 0

Abstract

DNA bend sites in the promoter region of the human estrogen receptor a gene were determined by the circular permutation assay. Among a total of five sites (ERB -4 to -1, and ERB + 1) mapped in the 3 kb region, three matched with the positions of the predicted periodicity while the other two did not. Most of the sites were accompanied by the short poly (dA)-poly (dT) tracts including the potential bend core sequence A2N8A2N8A2 (A/A/A). Fine mapping of the ERB-2 site indicated that this A/A/A and the immediate franking sequences contained motifs for the estrogen response element. This region had a higher affinity for the nuclear scaffold and was included in the core region of the nucleosome structure. However, binding of the nuclear factor(s) to the motifs and disruption of nucleosome structure occurred without ATP. These results suggest that a class of periodic bent DNA could act as a site of multiple interactions among the nuclear scaffold, core histones and nuclear factors.

[人类雌激素受体α基因启动子区域的DNA弯曲位点]。
用环形排列法测定了人雌激素受体a基因启动子区的DNA弯曲位点。在3kb区域共定位了5个位点(ERB -4 ~ -1和ERB + 1),其中3个位点与预测周期的位置匹配,另外2个位点与预测周期的位置不匹配。大部分位点均伴有短聚(dA)-聚(dT)链,包括潜在弯曲核序列A2N8A2N8A2 (A/A/A)。对ERB-2位点的精细定位表明,该A/A/A和直接标记序列包含雌激素反应元件的基序。该区域对核支架具有较高的亲和力,位于核小体结构的核心区域。然而,核因子与基序的结合和核小体结构的破坏在没有ATP的情况下发生。这些结果表明一类周期性弯曲DNA可能作为核支架、核心组蛋白和核因子之间多重相互作用的位点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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