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核因子-κB的DNA结合亚基与因子KBF1相同,且与rel癌基因产物同源。

The DNA binding subunit of NF-kappa B is identical to factor KBF1 and homologous to the rel oncogene product.

作者信息

Kieran M, Blank V, Logeat F, Vandekerckhove J, Lottspeich F, Le Bail O, Urban M B, Kourilsky P, Baeuerle P A, Israël A

机构信息

Unité de Biologie Moléculaire du Gène, U.277 INSERM, U.A.C. 115 CNRS, Institut Pasteur, Paris, France.

出版信息

Cell. 1990 Sep 7;62(5):1007-18. doi: 10.1016/0092-8674(90)90275-j.

Abstract

The major determinant in the transcriptional control of class I genes of the major histocompatibility complex is an enhancer sequence located around -170 from the transcription start site, which binds a factor named KBF1. We have isolated a complementary cDNA coding for KBF1 and identified the DNA binding and dimerization domain of the protein. Because KBF1 and the transcription factor NF-kappa B bind to similar sequences, we investigated the relationship between these two molecules. It appeared that KBF1 is, by all criteria used, identical to the 50 kd DNA binding subunit of NF-kappa B. KBF1 (and therefore p50) also displays extensive amino acid sequence homology with the v-rel oncogene and the Drosophila maternal morphogen dorsal. In vitro experiments suggest functional homologies between KBF1 and v-rel.

摘要

主要组织相容性复合体I类基因转录控制的主要决定因素是位于转录起始位点约-170处的一个增强子序列,它能结合一种名为KBF1的因子。我们分离出了编码KBF1的互补cDNA,并鉴定了该蛋白的DNA结合和二聚化结构域。由于KBF1和转录因子NF-κB能结合相似的序列,我们研究了这两种分子之间的关系。结果表明,根据所使用的所有标准,KBF1与NF-κB的50kd DNA结合亚基相同。KBF1(因此p50)与v-rel癌基因和果蝇母体形态发生素背侧蛋白也显示出广泛的氨基酸序列同源性。体外实验表明KBF1和v-rel之间存在功能同源性。

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