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Selection of DNA binding sites by regulatory proteins: the LexA protein and the arginine repressor use different strategies for functional specificity.

机译:通过调节蛋白选择DNA结合位点:LexA蛋白和精氨酸阻遏物使用不同的策略来实现功能特异性。

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摘要

The DNA sequences in the operator sites of the arginine regulon and of the SOS regulon have been subject to a statistical analysis. A quantitative correlation is found between the statistics of sequence choice and the activity at individual operator sites in both systems, as expected from theoretical considerations [Berg & von Hippel, J.Mol.Biol. (1987) 193, 723-750]. Based on these correlations it is possible to predict the effect of various sequence mutations. There is a significant difference in the slopes of the correlation lines between sequence and activity for the two systems. From this difference it can be expected that individual point mutations in the ARG boxes will have a much smaller effect on activity than similar changes in the SOS boxes. This difference may be related to a strong cooperative activity at tandem ARG boxes while the binding at SOS boxes appears to be mostly noncooperative.
机译:精氨酸调节子和SOS调节子的操作位点的DNA序列已经过统计分析。正如理论上的预期[Berg&von Hippel,J.Mol.Biol。 (1987)193,723-750]。基于这些相关性,可以预测各种序列突变的影响。两个系统的序列和活动之间的相关线斜率存在显着差异。根据这种差异,可以预期ARG盒中的单个点突变对活动的影响将比SOS盒中的类似变化小得多。这种差异可能与串联ARG盒上的强大协作活性有关,而SOS盒上的绑定似乎大部分是不协作的。

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