Hassa P O, Hottiger M O
Institute of Veterinary Biochemistry, University of Zürich, Switzerland.
Biol Chem. 1999 Jul-Aug;380(7-8):953-9. doi: 10.1515/BC.1999.118.
The transcription factor NF-kappaB plays a critical role in immune and inflammatory responses. Here we show that poly (ADP ribose) polymerase (PARP) is required for specific NF-kappaB transcriptional activation in vivo. The activation of the HIV-LTR promoter and an NF-kappaB-dependent artificial promoter was drastically reduced in PARP (-/-) cells, independently of the signaling pathway through which NF-kappaB was induced. Furthermore NF-kappaB-dependent gene activation was restored in vivo by the expression of PARP in PARP (-/-) cells. Finally, we show that both NF-kappaB and PARP formed a stable immunoprecipitable nuclear complex. This interaction did not need DNA binding. Our results suggest that PARP is an important cofactor in the activation cascade of NF-kappaB-dependent target genes.
转录因子NF-κB在免疫和炎症反应中起关键作用。在此我们表明,聚(ADP核糖)聚合酶(PARP)在体内特异性NF-κB转录激活中是必需的。HIV-LTR启动子和一个NF-κB依赖性人工启动子的激活在PARP(-/-)细胞中显著降低,与诱导NF-κB的信号通路无关。此外,通过在PARP(-/-)细胞中表达PARP,体内NF-κB依赖性基因激活得以恢复。最后,我们表明NF-κB和PARP都形成了一种稳定的可免疫沉淀的核复合物。这种相互作用不需要DNA结合。我们的结果表明,PARP是NF-κB依赖性靶基因激活级联中的一个重要辅助因子。