Sequence-Specific B-DNA Flexibility Modulates Z-DNA Formation

被引:30
|
作者
Bothe, Jameson R. [1 ]
Lowenhaupt, Ky [2 ]
Al-Hashimi, Hashim M. [1 ]
机构
[1] Univ Michigan, Dept Chem & Biophys, Ann Arbor, MI 48109 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
NMR-SPECTROSCOPY; SPIN RELAXATION; Z TRANSITION; DYNAMICS; JUNCTION; DECAMER; FIELDS; DOMAIN;
D O I
10.1021/ja1073068
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Conversion of right-handed B-DNA into left-handed Z-DNA is one of the largest structural transitions in biology that plays fundamental roles in gene expression and regulation. Z-DNA segments must form within genomes surrounded by a sea of B-DNA and require creation of energetically costly B/Z junctions. Here, we show using a combination of natural abundance NMR R1(rho) carbon relaxation measurements and CD spectroscopy that sequence-specific B-DNA flexibility modulates the thermodynamic propensity to form Z-DNA and the location of B/Z junctions. We observe sequence-specific flexibility in B-DNA spanning fast (ps-ns) and slow (mu s-ms) time scales localized at the site of B/Z junction formation. Further, our studies show that CG-repeats play an active role tuning this intrinsic B-DNA flexibility. Taken together, our results suggest that sequence-specific B-DNA flexibility may provide a mechanism for defining the length and location of Z-DNA in genomes.
引用
收藏
页码:2016 / 2018
页数:3
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