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Pho4酸性激活结构域对染色质调控和转录激活的要求。

Requirements for chromatin modulation and transcription activation by the Pho4 acidic activation domain.

作者信息

McAndrew P C, Svaren J, Martin S R, Hörz W, Goding C R

机构信息

Eukaryotic Transcription Laboratory, Marie Curie Research Institute, The Chart, Oxted, Surrey RH8 0TL, United Kingdom.

出版信息

Mol Cell Biol. 1998 Oct;18(10):5818-27. doi: 10.1128/MCB.18.10.5818.

Abstract

Perhaps the best characterized example of an activator-induced chromatin transition is found in the activation of the Saccharomyces cerevisiae acid phosphatase gene PHO5 by the basic helix-loop-helix (bHLH) transcription factor Pho4. Transcription activation of the PHO5 promoter by Pho4 is accompanied by the remodeling of four positioned nucleosomes which is dependent on the Pho4 activation domain but independent of transcription initiation. Whether the requirements for transcription activation through the TATA sequence are different from those necessary for the chromatin transition remains a major outstanding question. In an attempt to understand better the ability of Pho4 to activate transcription and to remodel chromatin, we have initiated a detailed characterization of the Pho4 activation domain. Using both deletion and point mutational analysis, we have defined residues between positions 75 and 99 as being both essential and sufficient to mediate transcription activation. Significantly, there is a marked concordance between the ability of mutations in the Pho4 activation domain to induce chromatin opening and transcription activation. Interestingly, the requirements for transcription activation within the Pho4 activation domain differ significantly if fused to a heterologous bHLH-leucine zipper DNA-binding domain. The implications for transcription activation by Pho4 are discussed.

摘要

或许,激活剂诱导的染色质转变的最佳特征实例见于碱性螺旋-环-螺旋(bHLH)转录因子Pho4对酿酒酵母酸性磷酸酶基因PHO5的激活过程。Pho4对PHO5启动子的转录激活伴随着四个定位核小体的重塑,这一重塑依赖于Pho4激活结构域,但与转录起始无关。通过TATA序列进行转录激活的要求与染色质转变所需的要求是否不同,仍是一个主要的悬而未决的问题。为了更好地理解Pho4激活转录和重塑染色质的能力,我们已开始对Pho4激活结构域进行详细表征。通过缺失和点突变分析,我们确定75至99位之间的残基对于介导转录激活既是必需的也是充分足够的。值得注意的是,Pho4激活结构域中的突变诱导染色质开放和转录激活的能力之间存在明显的一致性。有趣的是,如果与异源bHLH-亮氨酸拉链DNA结合结构域融合,Pho4激活结构域内转录激活的要求会有显著差异。本文讨论了Pho4转录激活的意义。

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