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核小体定位调节调节蛋白对小鼠乳腺肿瘤病毒启动子的可及性。

Nucleosome positioning modulates accessibility of regulatory proteins to the mouse mammary tumor virus promoter.

作者信息

Piña B, Brüggemeier U, Beato M

机构信息

Institut für Molekularbiologie und Tumorforschung, Marburg, Federal Republic of Germany.

出版信息

Cell. 1990 Mar 9;60(5):719-31. doi: 10.1016/0092-8674(90)90087-u.

Abstract

Minichromosomes containing the MMTV hormone responsive element (HRE) exhibit precisely positioned nucleosomes. Chromatin reconstitution of short HRE DNA fragments also results in precise positioning of nucleosomes as revealed by footprinting, which suggests that information for nucleosome phasing is contained within this short sequence. While hormone receptors bind naked DNA and reconstituted nucleosomes with similar affinities (3- to 5-fold difference), NFI, a transcription factor essential for efficient utilization of the MMTV promoter, binds naked DNA very tightly but does not bind the nucleosomally organized promoter. Hormone receptor binding to the MMTV nucleosome does not dissociate the nucleosome but leads to greater accessibility of the promoter-proximal end to exonuclease III. Precise positioning of one nucleosome over the MMTV promoter could repress transcription by preventing NFI binding in the absence of hormone, while still allowing interaction of activated hormone receptor with HRE.

摘要

含有小鼠乳腺肿瘤病毒激素反应元件(HRE)的微型染色体呈现出精确排列的核小体。短HRE DNA片段的染色质重建也导致核小体的精确定位,这通过足迹法得以揭示,这表明核小体相位信息包含在这个短序列中。虽然激素受体以相似的亲和力(3至5倍差异)结合裸露DNA和重建的核小体,但NFI(一种有效利用MMTV启动子所必需的转录因子)非常紧密地结合裸露DNA,但不结合核小体组织化的启动子。激素受体与MMTV核小体的结合不会使核小体解离,但会导致启动子近端对外切核酸酶III的可及性增加。在没有激素的情况下,一个核小体在MMTV启动子上的精确定位可通过阻止NFI结合来抑制转录,同时仍允许活化的激素受体与HRE相互作用。

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