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人类基因6-16的干扰素反应元件

Interferon response element of the human gene 6-16.

作者信息

Porter A C, Chernajovsky Y, Dale T C, Gilbert C S, Stark G R, Kerr I M

机构信息

Imperial Cancer Research Fund Laboratories, Lincoln's Inn Fields, London, UK.

出版信息

EMBO J. 1988 Jan;7(1):85-92. doi: 10.1002/j.1460-2075.1988.tb02786.x.

Abstract

1046 base-pairs (bp) of genomic DNA spanning the first exon of the human alpha/beta-interferon (IFN)-inducible gene 6-16 have been analysed for their role in induction. The whole gene or 5'-flanking deletion derivatives of it were assayed for inducibility in populations of stably transfected mouse cells. 5'-Flanking DNA fragments were assayed for their ability to confer inducibility on a reporter gene in stably and transiently transfected mouse and human cells. The data suggest that a 39 bp sequence is sufficient to confer transcriptional inducibility and can account in large part for the response of 6-16. Two copies of this sequence, one of which contains a dinucleotide insert, are located in tandem 88 bp upstream of the 6-16 transcriptional initiation site. For at least one of the repeat units the 5' limit of a subregion required for induction lies in the sequence GGGAAAAT. The motif GGAAA occurs in several well characterized enhancers. Furthermore, one residue 3' of the GGAAA there is a second motif, TGAAACT, which is conserved in the regulatory regions of other IFN-induced genes. In gel retardation assays the oligonucleotide GGGAAAATGAAACT competes with the repeat element for binding to IFN-modulated protein(s) but a mutated oligonucleotide, GGGAAAATGACACT does not. These results identify an alpha/beta IFN response element partially homologous to those described previously for the genes of the MHC complexes.

摘要

对跨越人类α/β干扰素(IFN)诱导基因6 - 16第一个外显子的1046个碱基对(bp)的基因组DNA进行了诱导作用分析。对整个基因或其5'侧翼缺失衍生物在稳定转染的小鼠细胞群体中进行诱导性检测。对5'侧翼DNA片段在稳定和瞬时转染的小鼠及人类细胞中赋予报告基因诱导性的能力进行检测。数据表明,一个39 bp的序列足以赋予转录诱导性,并且在很大程度上可以解释6 - 16的反应。该序列的两个拷贝,其中一个包含一个二核苷酸插入,串联位于6 - 16转录起始位点上游88 bp处。对于至少一个重复单元,诱导所需亚区域的5'边界位于序列GGGAAAAT中。基序GGAAA存在于几个特征明确的增强子中。此外,在GGAAA的3'端有一个第二个基序,TGAAACT,它在其他IFN诱导基因的调控区域中保守。在凝胶阻滞试验中,寡核苷酸GGGAAAATGAAACT与重复元件竞争结合IFN调节蛋白,但突变的寡核苷酸GGGAAAATGACACT则不能。这些结果鉴定出一个α/β干扰素反应元件,它与先前描述的MHC复合体基因的反应元件部分同源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ede1/454218/721d74a07b2c/emboj00138-0088-a.jpg

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