Chen Yi-Ju, Johnson Stephanie, Mulligan Peter, Spakowitz Andrew J, Phillips Rob
Departments of Physics.
Biochemistry and Molecular Biophysics, Department of Biochemistry and Biophysics, University of California, San Francisco, CA 94158; and.
Proc Natl Acad Sci U S A. 2014 Dec 9;111(49):17396-401. doi: 10.1073/pnas.1415685111. Epub 2014 Nov 19.
Storage and retrieval of the genetic information in cells is a dynamic process that requires the DNA to undergo dramatic structural rearrangements. DNA looping is a prominent example of such a structural rearrangement that is essential for transcriptional regulation in both prokaryotes and eukaryotes, and the speed of such regulations affects the fitness of individuals. Here, we examine the in vitro looping dynamics of the classic Lac repressor gene-regulatory motif. We show that both loop association and loop dissociation at the DNA-repressor junctions depend on the elastic deformation of the DNA and protein, and that both looping and unlooping rates approximately scale with the looping J factor, which reflects the system's deformation free energy. We explain this observation by transition state theory and model the DNA-protein complex as an effective worm-like chain with twist. We introduce a finite protein-DNA binding interaction length, in competition with the characteristic DNA deformation length scale, as the physical origin of the previously unidentified loop dissociation dynamics observed here, and discuss the robustness of this behavior to perturbations in several polymer parameters.
细胞中遗传信息的存储和检索是一个动态过程,需要DNA经历显著的结构重排。DNA环化就是这种结构重排的一个突出例子,它对于原核生物和真核生物的转录调控都至关重要,而且这种调控的速度会影响个体的适应性。在这里,我们研究了经典的Lac阻遏蛋白基因调控基序的体外环化动力学。我们表明,DNA-阻遏蛋白连接处的环结合和解离都取决于DNA和蛋白质的弹性变形,并且环化和解环化速率都大致与环化J因子成比例,该因子反映了系统的变形自由能。我们用过渡态理论解释了这一观察结果,并将DNA-蛋白质复合物建模为具有扭曲的有效类蠕虫链。我们引入了一个有限的蛋白质-DNA结合相互作用长度,它与特征性的DNA变形长度尺度相互竞争,作为此处观察到的先前未被识别的环解离动力学的物理起源,并讨论了这种行为对几种聚合物参数扰动的稳健性。