Nourbakhsh M, Oumard A, Schwarzer M, Hauser H
Department of Gene Regulation and Differentiation, GBF, German Research Institute for Biotechnology, Braunschweig, Germany.
Eur Cytokine Netw. 2000 Sep;11(3):500-1.
The family of NF-kappaB/rel transcription factors regulates a variety of promoters through specific DNA-binding sites. Consistent with the role of NF-kappaB activation as a response to pathogens, it regulates the expression of immune modulating cytokines like interferon-beta3 (IFN-3). Transcriptional regulation of IFN-beta is characterized by strict constitutive repression and virus-mediated activation. A nuclear protein, called NRF (NF-kappaB repressing factor) silences constitutively the IFN-beta3 promoter by binding to the negative regulatory element (NRE). This control is achieved by a direct protein-protein interaction between NRF and proximal bound NF-kappaB factors preventing the transcriptional activation. After viral induction NRF still binds but does not any more exert its specific inhibition. NRE-related sequences found in a number of promoters like those of HIV-1, HTLV-1 and the genes of the IL-2Ralpha and IL-8 constitute functionally related silencer elements which repress the constitutive enhancing activity of NF-kappaB/rel-binding sites from these promoters.
NF-κB/rel转录因子家族通过特定的DNA结合位点调控多种启动子。与NF-κB激活作为对病原体的应答作用一致,它调控免疫调节细胞因子如干扰素-β3(IFN-3)的表达。IFN-β的转录调控特点是严格的组成性抑制和病毒介导的激活。一种名为NRF(NF-κB抑制因子)的核蛋白通过与负调控元件(NRE)结合,使IFN-β3启动子组成性沉默。这种调控是通过NRF与近端结合的NF-κB因子之间的直接蛋白质-蛋白质相互作用实现的,从而阻止转录激活。病毒诱导后,NRF仍然结合,但不再发挥其特异性抑制作用。在许多启动子中发现的与NRE相关的序列,如HIV-1、HTLV-1以及IL-2Rα和IL-8基因的启动子,构成了功能相关的沉默元件,可抑制这些启动子中NF-κB/rel结合位点的组成性增强活性。