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真核生物启动子区域中的S1超敏位点。

S1-hypersensitive sites in eukaryotic promoter regions.

作者信息

Evans T, Schon E, Gora-Maslak G, Patterson J, Efstratiadis A

出版信息

Nucleic Acids Res. 1984 Nov 12;12(21):8043-58. doi: 10.1093/nar/12.21.8043.

Abstract

We have examined by fine mapping the S1 nuclease-hypersensitivity of the 5' flanking regions of the human beta-globin and rat preproinsulin II genes and of the SV40 origin/enhancer region. In all cases S1-hypersensitive sites are located in known or presumed promoter/regulatory regions. Though a consensus DNA sequence is not evident, all of these sites reside in predominantly homopurine-homopyrimidine stretches. The alternate (non-B) DNA structure which is revealed by the enzymatic probe is a sequence-dependent feature of a short stretch of DNA, which is retained upon transplantation into a foreign environment. The alternate structure exhibits S1-nicking patterns uniquely different from those associated with the presence of Z-DNA.

摘要

我们通过精细定位,研究了人类β-珠蛋白基因、大鼠胰岛素原II基因5'侧翼区域以及SV40病毒起源/增强子区域的S1核酸酶超敏反应。在所有情况下,S1超敏位点均位于已知或推测的启动子/调控区域。尽管尚未发现一致的DNA序列,但所有这些位点主要位于同型嘌呤-同型嘧啶序列中。酶促探针所揭示的交替(非B型)DNA结构是一小段DNA的序列依赖性特征,该特征在移植到外源环境中后仍能保留。这种交替结构呈现出与Z-DNA存在相关的独特不同的S1切口模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8afa/320272/6f8f75f089ac/nar00339-0094-a.jpg

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