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肿瘤坏死因子通过诱导一种能取代组成型因子的类核因子κB增强子结合活性,刺激小鼠MHC I类基因的表达。

TNF stimulates expression of mouse MHC class I genes by inducing an NF kappa B-like enhancer binding activity which displaces constitutive factors.

作者信息

Israël A, Le Bail O, Hatat D, Piette J, Kieran M, Logeat F, Wallach D, Fellous M, Kourilsky P

机构信息

Unité de Biologie Moléculaire du Gène, U.277 INSERM, Paris, France.

出版信息

EMBO J. 1989 Dec 1;8(12):3793-800. doi: 10.1002/j.1460-2075.1989.tb08556.x.

Abstract

We have dissected the mouse H-2Kb gene promoter in order to define the sequences responsible for induction by tumour necrosis factor (TNF-alpha). An enhancer element (-187 to -158) composed of two imperfect direct palindromic repeats has been shown to be necessary and sufficient for TNF-alpha induction of a heterologous promoter. A multimer of either repeat is also responsive, while a single copy is not: this is the situation in the beta 2-microglobulin (beta 2-m) promoter which contains a single palindrome and does not respond to TNF-alpha. We had previously found that the two repeats can bind a factor named KBF1. We show here that in the uninduced state the transcription factor AP2 binds to the interpalindromic region, while in TNF-treated cells an NF kappa B-like activity is induced which displaces both KBF1 and AP2 and binds to the two palindromes. This strongly suggests that induction of an NF kappa B-like activity is responsible for TNF-alpha stimulation of mouse MHC class I genes.

摘要

为了确定负责肿瘤坏死因子(TNF-α)诱导的序列,我们对小鼠H-2Kb基因启动子进行了剖析。由两个不完全直接回文重复序列组成的增强子元件(-187至-158)已被证明对于TNF-α诱导异源启动子是必要且充分的。任一重复序列的多聚体也有反应,而单拷贝则无反应:β2-微球蛋白(β2-m)启动子就是这种情况,它含有一个单一回文序列,对TNF-α无反应。我们之前发现这两个重复序列能结合一种名为KBF1的因子。我们在此表明,在未诱导状态下,转录因子AP2结合到回文序列间区域,而在TNF处理的细胞中,诱导出一种NF-κB样活性,它取代了KBF1和AP2并结合到两个回文序列上。这强烈表明,NF-κB样活性的诱导是TNF-α刺激小鼠MHC I类基因的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e27b/402065/0ce13c41bf3a/emboj00136-0246-a.jpg

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