Multilevel Deconstruction of the In Vivo Behavior of Looped DNA-Protein Complexes

被引:24
作者
Saiz, Leonor [1 ]
Vilar, Jose M. G. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Computat Biol Program, Integrat Biol Modeling Lab, New York, NY 10021 USA
来源
PLOS ONE | 2007年 / 2卷 / 04期
关键词
D O I
10.1371/journal.pone.0000355
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Protein-DNA complexes with loops play a fundamental role in a wide variety of cellular processes, ranging from the regulation of DNA transcription to telomere maintenance. As ubiquitous as they are, their precise in vivo properties and their integration into the cellular function still remain largely unexplored. Here, we present a multilevel approach that efficiently connects in both directions molecular properties with cell physiology and use it to characterize the molecular properties of the looped DNA-lac repressor complex while functioning in vivo. The properties we uncover include the presence of two representative conformations of the complex, the stabilization of one conformation by DNA architectural proteins, and precise values of the underlying twisting elastic constants and bending free energies. Incorporation of all this molecular information into gene-regulation models reveals an unprecedented versatility of looped DNA-protein complexes at shaping the properties of gene expression.
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页数:7
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