DNA Architecture, Deformability, and Nucleosome Positioning

被引:28
作者
Xu, Fei [1 ]
Olson, Wilma K. [1 ]
机构
[1] Rutgers State Univ, Dept Chem & Chem Biol, BioMaPS Inst Quantitat Biol, Wright Rieman Labs, Piscataway, NJ 08854 USA
关键词
DNA deformation; Minor-groove width; Nucleosome positioning; Sequence threading; CORE PARTICLE; CRYSTAL-STRUCTURE; HISTONE; CHROMATIN; BINDING; DATABASE; COMPLEX; MOTIFS;
D O I
10.1080/073911010010524943
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The positioning of DNA on nucleosomes is critical to both the organization and expression of the genetic message. Here we focus on DNA conformational signals found in the growing library of known high-resolution core-particle structures and the ways in which these features may contribute to the positioning of nucleosomes on specific DNA sequences. We survey the chemical composition of the protein-DNA assemblies and extract features along the DNA superhelical pathway the minor-groove width and the deformations of successive base pairs determined with reasonable accuracy in the structures. We also examine the extent to which the various nucleosome core-particle structures accommodate the observed settings of the crystallized sequences and the known positioning of the high-affinity synthetic '601' sequence on DNA. We 'thread' these sequences on the different structural templates and estimate the cost of each setting with knowledge-based potentials that reflect the conformational properties of the DNA base-pair steps in other high-resolution protein-bound complexes.
引用
收藏
页码:725 / 739
页数:15
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