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在小鼠α干扰素基因启动子中鉴定出一种新型病毒反应序列。

Identification of a novel virus-responsive sequence in the promoter of murine interferon-alpha genes.

作者信息

Raj N B, Au W C, Pitha P M

机构信息

Oncology Center, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.

出版信息

J Biol Chem. 1991 Jun 15;266(17):11360-5.

PMID:2040641
Abstract

We have previously shown that the infection of mouse L-cells with Newcastle disease virus activates transcription of the alpha 4 but not the alpha 6 interferon gene and that the induction is mediated by a 35-base pair inducible element (IE) found in the alpha 4 promoter (-109 to -75). In the present study, we show that the inactivity of the alpha 6 promoter can be mapped to 2 out of 6 nucleotides in which the alpha 6 differs from alpha 4 IE. The symmetrical sequence, GTAAAGAAAGT (-103 to -93), present in the alpha 4 IE is essential for its inducibility and binding of nuclear protein(s) to the alpha 4 IE.

摘要

我们之前已经表明,用新城疫病毒感染小鼠L细胞会激活α4干扰素基因的转录,但不会激活α6干扰素基因的转录,并且这种诱导是由α4启动子(-109至-75)中一个35个碱基对的诱导元件(IE)介导的。在本研究中,我们表明α6启动子的无活性可以定位到α6与α4 IE不同的6个核苷酸中的2个。α4 IE中存在的对称序列GTAAAGAAAGT(-103至-93)对其诱导性以及核蛋白与α4 IE的结合至关重要。

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