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作为一种生物控制机制的基因组调节蛋白的非特异性DNA结合:体内DNA结合的大肠杆菌乳糖阻遏物的测量。

Nonspecific DNA binding of genome-regulating proteins as a biological control mechanism: measurement of DNA-bound Escherichia coli lac repressor in vivo.

作者信息

Kao-Huang Y, Revzin A, Butler A P, O'Conner P, Noble D W, von Hippel P H

出版信息

Proc Natl Acad Sci U S A. 1977 Oct;74(10):4228-32. doi: 10.1073/pnas.74.10.4228.

Abstract

Binding of genome regulatory proteins to nonspecific DNA sites may play an important role in controlling the thermodynamics and kinetics of the interactions of these proteins with their specific target DNA sequences. An estimate of the fraction of Escherichia coli lac repressor molecules bound in vivo to the operator region and to nonoperator sites on the E. coli chromosome is derived by measurement of the distribution of repressor between a minicell-producing E. coli strain (P678-54) and the DNA-free minicells derived therefrom. Assuming the minicell cytoplasm to be representative of that of the parent E. coli cells, we find that less than 10% of the repressor tetramers of the average cell are free in solution; the remainder are presumed to be bound to the bacterial chromosome. The minimum in vivo value of the association constant for repressor to bulk nonoperator DNA (K(RD)) calculated from these results is about 10(3) M(-1), and analysis of the sources of error in the minicell experiment suggests that the actual in vivo value of K(RD) could be substantially greater. The value of K(RD), coupled with in vitro data on the ionic strength dependence of this parameter, can be used to estimate that the effective intracellular cation activity of E. coli is no greater than about 0.24 M (and probably no less than 0.17 M) in terms of sodium ion equivalents. The minicell distribution experiments also confirm that the association constant for the binding of inducer-repressor complex to bulk nonoperator DNA (K(RID)) is [unk] K(RD)in vivo. These results are used to calculate minimum in vivo values of K(RO) and K(RIO) (association constants for repressor and for inducer-repressor complex binding to operator) of about 10(12) M(-1) and about 10(9) M(-1), respectively. The results fit a quantitative model for operon regulation in which nonspecific DNA-repressor complexes play a key role in determining basal and constitutive levels of gene expression [von Hippel, P. H., Revzin, A., Gross, C. A. & Wang, A. C. (1974) Proc. Natl. Acad. Sci. USA 71, 4808-4812].

摘要

基因组调节蛋白与非特异性DNA位点的结合可能在控制这些蛋白与其特异性靶DNA序列相互作用的热力学和动力学方面发挥重要作用。通过测量产生微小细胞的大肠杆菌菌株(P678 - 54)和由此衍生的无DNA微小细胞之间阻遏物的分布,得出了大肠杆菌乳糖阻遏物分子在体内与操纵区及大肠杆菌染色体上非操纵位点结合的比例估计值。假设微小细胞的细胞质代表亲本大肠杆菌细胞的细胞质,我们发现平均细胞中不到10%的阻遏物四聚体在溶液中是游离的;其余的推测与细菌染色体结合。根据这些结果计算出的阻遏物与大量非操纵DNA(K(RD))的体内结合常数的最小值约为10³ M⁻¹,对微小细胞实验中误差来源的分析表明,K(RD)的实际体内值可能大得多。K(RD)的值,结合该参数对离子强度依赖性的体外数据,可用于估计大肠杆菌的有效细胞内阳离子活性以钠离子当量计不大于约0.24 M(可能不小于0.17 M)。微小细胞分布实验还证实,诱导剂 - 阻遏物复合物与大量非操纵DNA结合的结合常数(K(RID))在体内[未知]K(RD)。这些结果用于计算K(RO)和K(RIO)(阻遏物和诱导剂 - 阻遏物复合物与操纵子结合的结合常数)的体内最小值,分别约为10¹² M⁻¹和约10⁹ M⁻¹。这些结果符合操纵子调控的定量模型,其中非特异性DNA - 阻遏物复合物在确定基因表达的基础水平和组成水平方面起关键作用[冯·希佩尔,P. H.,雷夫津,A.,格罗斯,C. A. & 王,A. C.(1974年)美国国家科学院院刊71,4808 - 4812]。

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