Kralova J, Schatzle J D, Liss A S, Bargmann W, Bose H R
Department of Microbiology and the Cell Research Institute, University of Texas at Austin, Austin, TX 78712-1095, USA.
Oncogene. 1996 Jun 20;12(12):2595-604.
Rel/NF-kappa B transcription factors and I Kappa B alpha function in an autoregulatory network. Avian I kappa B alpha transcription is increased in response to both c-Rel and v-Rel. This study shows that I kappa B alpha transcription is synergistically stimulated by Rel and AP-1 factors (c-Fos and c-Jun). However, the response to v-Rel and the AP-1 factors was not as vigorous as that of c-Rel and AP-1. A 386 bp region of the I kappa B alpha promoter (containing two NF-kappa B and one AP-1 binding sites) was shown to be both necessary and sufficient for response to both Rel factors alone or Rel factors in conjunction with the AP-1 proteins. In addition, an imperfect NF-kappa B binding site was found to overlap the AP-1 binding site. Mutation of either of the NF-kappa B binding sites or the AP-1 binding site dramatically decreased the response of the I kappa B alpha promoter to Rel proteins alone or Rel and AP-1 factors. Overexpression of c-Rel or v-Rel resulted in the formation of DNA binding complexes associated with the imperfect NF-kappa B binding site which overlaps the AP-1 site. v-Rel associated with the imperfect NF-kappa B site stronger than c-Rel, and overexpression of v-Rel also resulted in the formation of a v-Rel containing complex bound to a consensus AP-1 site. These studies address the difference in c-Rel and v-Rel's ability to synergistically stimulate I kappa B alpha expression in conjunction with the AP-1 factors.
Rel/NF-κB转录因子和IκBα在一个自动调节网络中发挥作用。禽类IκBα转录在对c-Rel和v-Rel的反应中均会增加。本研究表明,IκBα转录受到Rel和AP-1因子(c-Fos和c-Jun)的协同刺激。然而,对v-Rel和AP-1因子的反应不如c-Rel和AP-1那样强烈。IκBα启动子的一个386 bp区域(包含两个NF-κB结合位点和一个AP-1结合位点)被证明对于单独对Rel因子或Rel因子与AP-1蛋白结合的反应既是必需的也是充分的。此外,发现一个不完全的NF-κB结合位点与AP-1结合位点重叠。NF-κB结合位点或AP-1结合位点中的任何一个发生突变都会显著降低IκBα启动子对单独Rel蛋白或Rel与AP-1因子的反应。c-Rel或v-Rel的过表达导致与与AP-1位点重叠的不完全NF-κB结合位点相关的DNA结合复合物的形成。v-Rel与不完全NF-κB位点的结合比c-Rel更强,并且v-Rel的过表达还导致形成一种与共有AP-1位点结合的包含v-Rel的复合物。这些研究探讨了c-Rel和v-Rel与AP-1因子协同刺激IκBα表达能力的差异。