Suppr超能文献

来自小鼠核糖体DNA的顺式作用序列促进质粒DNA在小鼠细胞中的扩增和持久性:高迁移率族蛋白I在其功能中的作用

Cis-acting sequences from mouse rDNA promote plasmid DNA amplification and persistence in mouse cells: implication of HMG-I in their function.

作者信息

Wegner M, Zastrow G, Klavinius A, Schwender S, Müller F, Luksza H, Hoppe J, Wienberg J, Grummt F

机构信息

Institut für Biochemie, Universität Würzburg, FRG.

出版信息

Nucleic Acids Res. 1989 Dec 11;17(23):9909-32. doi: 10.1093/nar/17.23.9909.

Abstract

Searching for amplification promoting sequences within the murine rDNA cistrons, we isolated two elements from the nontranscribed spacer region. These 370 bp and 423 bp long cis-acting elements, referred to as muNTS1 and muNTS2, are localized 4.1 kb and 4.6 kb upstream the RNA polymerase I transcriptional start site. They contain ca. 50 bp long AT-rich sequences that strongly interact with a protein from nuclear extracts. The protein could be purified and identified as HMG-I. A synthetic oligonucleotide encompassing the AT-rich stretch from muNTS1 is able to substitute for the muNTS elements. A similar sequence from the nontranscribed spacer of rat has previously been reported to be important for the function of the RNA polymerase I enhancer (1). Therefore the interaction of HMG I with the muNTS elements may play a role both in the stimulation of DNA amplification and transcription.

摘要

在小鼠rDNA顺反子内寻找促进扩增的序列时,我们从非转录间隔区分离出了两个元件。这些长度分别为370 bp和423 bp的顺式作用元件,称为muNTS1和muNTS2,位于RNA聚合酶I转录起始位点上游4.1 kb和4.6 kb处。它们含有约50 bp长的富含AT的序列,这些序列与核提取物中的一种蛋白质强烈相互作用。该蛋白质可以被纯化并鉴定为HMG-I。一个包含muNTS1中富含AT片段的合成寡核苷酸能够替代muNTS元件。先前报道,大鼠非转录间隔区的一个类似序列对RNA聚合酶I增强子的功能很重要(1)。因此,HMG I与muNTS元件的相互作用可能在DNA扩增和转录的刺激中都起作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验