首页> 外文期刊>Molecular and Cellular Biology >Capturing nuclear sequence-specific DNA-binding proteins by using simian virus 40-derived minichromosomes.
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Capturing nuclear sequence-specific DNA-binding proteins by using simian virus 40-derived minichromosomes.

机译:通过使用猿猴病毒40衍生的微型染色体捕获核序列特异性DNA结合蛋白。

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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.
机译:我们已经使用重组猿猴病毒40(SV40)微型染色体来检索从COS-7细胞的细胞核衍生的序列特异性DNA结合蛋白。我们显示转录因子AP-1和Sp1在病毒感染后期稳定地与SV40 DNA结合。在相似的条件下,携带大鼠胰岛素(rINS1)增强子的微型染色体在COS-7细胞中处于负调控状态,结合了两个蛋白质,它们映射到rINS1增强子的不同区域。 SV40 P元件竞争这些蛋白质中的一种,该蛋白质与-198至-230区域结合。此因素可能与AP-1有关。另一个因子选择性地结合胰岛素增强剂的-92至-124区域中的调节元件。这些蛋白质可能在调节rINS1增强子功能中发挥作用。

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