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Efficient chromosomal-scale DNA looping in Escherichia coli using multiple DNA-looping elements

机译:使用多个DNa环化元件在大肠杆菌中高效染色体规模的DNa循环

摘要

Genes are frequently regulated by interactions between proteins that bind to the DNA near the gene and proteins that bind to DNA sites located far away, with the intervening DNA looped out. But it is not understood how efficient looping can occur when the sites are very far apart. We develop a simple theoretical framework that relates looping efficiency to the energetic cost and benefit of looping, allowing prediction of the efficiency of single or multiple nested loops at different distances. Measurements of absolute loop efficiencies for Lac repressor and λ CI using gene expression reporters in Escherichia coli cells show that, as predicted by the model, long-range DNA looping between a pair of sites can be strongly enhanced by the use of nested DNA loops or by the use of additional protein-binding sequences. A combination of these approaches was able to generate efficient DNA looping at a 200 kb distance.
机译:经常通过与基因附近的DNA结合的蛋白质与与位于远处的DNA位置结合的蛋白质之间的相互作用调节基因,而中间的DNA则被圈出。但是,还不了解当站点相距很远时如何有效地循环。我们开发了一个简单的理论框架,将循环效率与循环的能量成本和收益相关联,从而可以预测不同距离处的单个或多个嵌套循环的效率。使用基因表达报告基因在大肠杆菌细胞中对Lac阻遏物和λCI的绝对环效率的测量表明,如模型所预测的,可通过使用嵌套DNA环或双链环极大地增强一对位点之间的远距离DNA环。通过使用其他蛋白质结合序列。这些方法的组合能够在200 kb的距离处产生有效的DNA环。

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