首页> 外文期刊>Journal of Biomolecular Structure and Dynamics >The affinity of DNA sequences containing R5Y5 motif and TA repeats with 10.5-bp periodicity to histone octamer in vitro
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The affinity of DNA sequences containing R5Y5 motif and TA repeats with 10.5-bp periodicity to histone octamer in vitro

机译:含有R5Y5基序和TA的DNA序列的亲和力,TA在体外对组蛋白八寡发酮的10.5bp周期性重复

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摘要

Nucleosome positioning along the genome is partially determined by the intrinsic DNA sequence preferences on histone. RRRRRYYYYY (R5Y5, R=Purine and Y=Pyrimidine) motif in nucleosome DNA, which was presented based on several theoretical models by Trifonov etal., might be a facilitating sequence pattern for nucleosome assembly. However, there is not a high conformity experimental evidence to support the concept that R5Y5 motif is a key element for the determination of nucleosome positioning. In this work, the ability of the canonical, H2A.Z- and H3.3-containing octamers to assemble nucleosome on DNA templates containing R5Y5 motif and TA repeats within 10.5-bp periodicity was investigated by using salt-dialysis method in vitro. The results showed that the10.5-bp periodical distributions of both R5Y5 motif and TA repeats along DNA templates can significantly promote canonical nucleosome assembly and may be key sequence factors for canonical nucleosome assembly. Compared with TA repeats within 10.5-bp periodicity, R5Y5 motif in DNA templates did not elevate H2A.Z- and H3.3-containing nucleosome formation efficiency in vitro. This result indicates that R5Y5 motif probably isn't a pivotal factor to regulate nucleosome assembly on histone variants. It is speculated that the regulatory mechanism of nucleosome assembly is different between canonical and variant histone. These conclusions can provide a deeper insight on the mechanism of nucleosome positioning.Communicated by Ramaswamy H. Sarma
机译:沿着基因组的核小体定位部分通过组蛋白的内在DNA序列偏好部分确定。核小组DNA中的rRrrryyyyy(R5Y5,R =嘌呤和y =嘧啶)基序基于Trifonov Etal的几种理论模型提出。,可能是核心组件的促进序列模式。然而,没有高度符合性的实验证据来支持R5Y5基序是核心定位的关键要素的概念。在这项工作中,通过在体外使用盐透析法研究了含有R5Y5基序和TA重复的含有R5Y5基序和TA重复的含有R5Y5基序和TA重复的含有R5Y5基序和TA重复的核心的能力。结果表明,沿DNA模板的R5Y5​​基序和TA重复的10.5bp周期分布可以显着促进规范核小组件,并且可以是规范核心组装的关键序列因子。与10.5-BP周期内的Ta重复相比,DNA模板中的R5Y5​​基序没有在体外升高H2A.Z-和含H3.3的核微粒形成效率。该结果表明R5Y5基序可能不是调节组蛋白变体上的核心组装的枢转因子。试图推测核心组件的调节机制在规范和变体组蛋白之间是不同的。这些结论可以深入了解ramaswamy H. Sarma的Nucleosome定位的机制。

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