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干扰素诱导因子与介导转录激活的寡核苷酸的差异结合。

Differential binding of interferon-induced factors to an oligonucleotide that mediates transcriptional activation.

作者信息

Reich N C, Darnell J E

机构信息

Laboratory of Molecular Cell Biology, Rockefeller University, New York, NY 10021.

出版信息

Nucleic Acids Res. 1989 May 11;17(9):3415-24. doi: 10.1093/nar/17.9.3415.

Abstract

Type I interferons elicit a number of biological responses by rapidly and transiently stimulating the transcriptional expression of a specific set of genes. The promoters of the inducible genes contain an enhancer element which is required for transcriptional activation. A specific oligonucleotide of 18 residues is sufficient for transcriptional induction when positioned in a heterologous promoter. Previous studies have identified three protein factors which can bind to the interferon stimulated enhancer. We show here that the binding of one of the interferon-induced factors requires specific nucleotides flanking the minimum recognition site for the other two factors. The distinct interaction of this factor with the response element is of significant importance since this factor is the sole candidate for a primary transcriptional activator of interferon-induced genes.

摘要

I型干扰素通过快速且短暂地刺激一组特定基因的转录表达引发多种生物学反应。可诱导基因的启动子包含一个转录激活所需的增强子元件。当置于异源启动子中时,一个18个残基的特定寡核苷酸足以诱导转录。先前的研究已鉴定出三种可与干扰素刺激增强子结合的蛋白质因子。我们在此表明,其中一种干扰素诱导因子的结合需要另外两种因子的最小识别位点两侧的特定核苷酸。该因子与反应元件的独特相互作用至关重要,因为该因子是干扰素诱导基因的主要转录激活因子的唯一候选者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc05/317784/cbacee734ffc/nar00126-0093-a.jpg

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