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DNA的序列特异性识别。野生型和突变型λOR3操纵子DNA的核磁共振归属及结构比较。

Sequence-specific recognition of DNA. Nuclear magnetic resonance assignments and structural comparison of wild-type and mutant lambda OR3 operator DNA.

作者信息

Wemmer D E, Chou S H, Reid B R

出版信息

J Mol Biol. 1984 Nov 25;180(1):41-60. doi: 10.1016/0022-2836(84)90429-7.

DOI:10.1016/0022-2836(84)90429-7
PMID:6096560
Abstract

The resonances of all the base protons and most of the sugar protons in both strands of the 17 base-pair OR3 operator of the phage lambda, and of the vC3 single base-pair mutant, have been assigned using two-dimensional nuclear magnetic resonance methods. The chemical shift and nuclear Overhauser effect data for these two DNA sequences reveal no structural perturbation at sites distal to the mutation, neither are there significant changes in structure immediately surrounding the altered base-pair in the mutant sequence. These results are consistent with the model proposed by Ohlendorf et al. (1982), based on crystallographic data on the cro protein, for the OR3-cro protein interaction. The data from these solution studies are examined and discussed in the light of this model. This work demonstrates that nuclear magnetic resonance chemical shifts and nuclear Overhauser effect intensities provide a method for comparing the solution structures of DNA molecules. From the resolution available in the spectra of the 17 base-pair operators studied, it is clear that DNA duplexes of up to 30 or more base-pairs can be studied using phase-sensitive methods.

摘要

利用二维核磁共振方法,已对噬菌体λ的17个碱基对的OR3操纵基因两条链中所有碱基质子以及大部分糖质子的共振峰进行了归属,同时也对vC3单碱基对突变体进行了同样的操作。这两个DNA序列的化学位移和核Overhauser效应数据显示,在突变位点远端没有结构扰动,突变序列中被改变的碱基对周围的结构也没有显著变化。这些结果与Ohlendorf等人(1982年)基于cro蛋白晶体学数据提出的OR3 - cro蛋白相互作用模型一致。根据该模型对这些溶液研究的数据进行了检验和讨论。这项工作表明,核磁共振化学位移和核Overhauser效应强度为比较DNA分子的溶液结构提供了一种方法。从所研究的17个碱基对操纵基因的光谱分辨率来看,很明显可以使用相敏方法研究多达30个或更多碱基对的DNA双链体。

相似文献

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Sequence-specific recognition of DNA. Nuclear magnetic resonance assignments and structural comparison of wild-type and mutant lambda OR3 operator DNA.DNA的序列特异性识别。野生型和突变型λOR3操纵子DNA的核磁共振归属及结构比较。
J Mol Biol. 1984 Nov 25;180(1):41-60. doi: 10.1016/0022-2836(84)90429-7.
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Nucleic Acids Res. 1984 Apr 25;12(8):3551-61. doi: 10.1093/nar/12.8.3551.
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Eur Biophys J. 1985;12(2):87-95. doi: 10.1007/BF00260431.
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[Study of the structure of phage lambda operator OR1 using two-dimensional 1H-NMR-spectroscopy].
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Solution structure of phage lambda half-operator DNA by use of NMR, restrained molecular dynamics, and NOE-based refinement.利用核磁共振、受限分子动力学和基于核欧沃豪斯效应的精修法对噬菌体λ半操纵基因DNA的溶液结构进行研究。
Biochemistry. 1990 May 22;29(20):4828-39. doi: 10.1021/bi00472a012.

引用本文的文献

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Nucleic Acids Res. 1985 May 24;13(10):3755-72. doi: 10.1093/nar/13.10.3755.
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Two-dimensional NMR investigation of a bent DNA fragment: assignment of the proton resonances and preliminary structure analysis.弯曲DNA片段的二维核磁共振研究:质子共振归属及初步结构分析
Nucleic Acids Res. 1987 Jul 24;15(14):5845-62. doi: 10.1093/nar/15.14.5845.
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OR3 operator of bacteriophage lambda in a 23 base-pair DNA fragment: sequence-specific 1H NMR assignments for the non-labile protons and comparison with the isolated 17 base-pair operator.
噬菌体λ的OR3操纵子位于一个23个碱基对的DNA片段中:非不稳定质子的序列特异性¹H NMR归属以及与分离出的17个碱基对操纵子的比较
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4
Resonance assignments of non-exchangeable protons in B type DNA oligomers, an overview.B型DNA寡聚物中不可交换质子的共振归属概述
Nucleic Acids Res. 1988 Jul 11;16(13):5713-26. doi: 10.1093/nar/16.13.5713.
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Flanking DNA-sequences contribute to the specific binding of cI-repressor and OR1.侧翼DNA序列有助于cI阻遏蛋白与OR1的特异性结合。
Nucleic Acids Res. 1989 May 25;17(10):3747-55. doi: 10.1093/nar/17.10.3747.
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High-resolution NMR studies of chimeric DNA-RNA-DNA duplexes, heteronomous base pairing, and continuous base stacking at junctions.嵌合DNA-RNA-DNA双链体、异源碱基配对以及连接处连续碱基堆积的高分辨率核磁共振研究。
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