Nir U, Fodor E, Rutter W J
Hormone Research Institute, University of California, San Francisco 94143-0534.
Mol Cell Biol. 1988 Feb;8(2):982-7. doi: 10.1128/mcb.8.2.982-987.1988.
We have used recombinant simian virus 40 (SV40) minichromosomes to retrieve sequence-specific DNA-binding proteins derived from the cell nucleus of COS-7 cells. We showed that the transcription factors AP-1 and Sp1 are stably bound to the SV40 DNA late in viral infection. Under similar conditions, minichromosomes carrying the rat insulin (rINS1) enhancer, which is under negative regulation in COS-7 cells, bound two proteins which mapped to distinct regions of the rINS1 enhancer. The SV40 P element competed for one of these proteins which bound to the region from -198 to -230. This factor may be related to AP-1. The other factor selectively bound a regulatory element in the region from -92 to -124 of the insulin enhancer. These proteins may play a role in regulating the rINS1 enhancer function.
我们利用重组猿猴病毒40(SV40)微型染色体从COS-7细胞核中获取序列特异性DNA结合蛋白。我们发现转录因子AP-1和Sp1在病毒感染后期稳定结合于SV40 DNA。在相似条件下,携带大鼠胰岛素(rINS1)增强子的微型染色体(该增强子在COS-7细胞中处于负调控状态)结合了两种蛋白,它们定位于rINS1增强子的不同区域。SV40 P元件竞争其中一种与-198至-230区域结合的蛋白。该因子可能与AP-1相关。另一种因子选择性结合胰岛素增强子-92至-124区域的一个调控元件。这些蛋白可能在调节rINS1增强子功能中发挥作用。