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热休克蛋白70(hsp70)启动子的染色质增强与GAGA因子的募集有关。

Chromatin potentiation of the hsp70 promoter is linked to GAGA-factor recruitment.

作者信息

Georgel Philippe T

机构信息

Department of Biological Sciences, Marshall University, Huntington, WV 25755, USA.

出版信息

Biochem Cell Biol. 2005 Aug;83(4):555-65. doi: 10.1139/o05-060.

Abstract

The events leading to transcription initiation of the Drosophila melanogaster heat-shock protein (hsp)70 gene have been demonstrated to be directly connected with nucleosome remodeling factor and GAGA-dependent chromatin remodeling on its promoter region. To investigate the relative importance of the multiple GAGA-factor binding sites in the process of chromatin remodeling and their effect on DNA conformation, the position of nucleosomes over the proximal region of the promoter was mapped. No real-positioned nucleosome was detected. By matching the relative position of the GAGA-factor binding sites with the distribution of nucleosomes over the hsp70 promoter, the GAGA site 2 appeared to be the most accessible, i.e., located close to a nucleosomal edge or within the linker DNA. This result, combined with previous observations, suggest a link between increased GAGA-factor accessibility and efficiency of transcription initiation. The effect of GAGA-binding-site mutations, both individually and in combination, on DNA structure and nucleosome remodeling was assessed using free DNA and fly embryo extract chromatin templates assembled in vitro. Results indicated that both the number of functional sites and their positions within the chromatin were important determinants for nucleosome-remodeling efficiency. Ultimately, the degree of accessibility of the GAGA factor to its cognate binding site(s) appears to be proportional to chromatin-remodeling competency of the hsp70 promoter.

摘要

导致果蝇热休克蛋白(hsp)70基因转录起始的事件已被证明与核小体重塑因子以及其启动子区域上依赖GAGA的染色质重塑直接相关。为了研究多个GAGA因子结合位点在染色质重塑过程中的相对重要性及其对DNA构象的影响,绘制了启动子近端区域上核小体的位置。未检测到真正定位的核小体。通过将GAGA因子结合位点的相对位置与hsp70启动子上核小体的分布相匹配,GAGA位点2似乎是最易接近的,即位于靠近核小体边缘或连接DNA内。这一结果与先前的观察结果相结合,表明GAGA因子可及性增加与转录起始效率之间存在联系。使用体外组装的游离DNA和果蝇胚胎提取物染色质模板,评估了GAGA结合位点突变单独和组合对DNA结构和核小体重塑的影响。结果表明,功能位点的数量及其在染色质中的位置都是核小体重塑效率的重要决定因素。最终,GAGA因子与其同源结合位点的可及程度似乎与hsp70启动子的染色质重塑能力成正比。

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