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体外实验中含 R5Y5 基序和 TA 重复序列的 DNA 序列与组蛋白八聚体的亲和力为 10.5bp 周期性。

The affinity of DNA sequences containing R5Y5 motif and TA repeats with 10.5-bp periodicity to histone octamer in vitro.

机构信息

a School of Life Science and Technology , Inner Mongolia University of Science and Technology , Baotou , China.

b Inner Mongolia Key Laboratory of Functional Genome Bioinformatics , Inner Mongolia University of Science and Technology , Baotou , China.

出版信息

J Biomol Struct Dyn. 2019 May;37(8):1935-1943. doi: 10.1080/07391102.2018.1477621. Epub 2018 Nov 1.

Abstract

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 et al., 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.

摘要

核小体在基因组上的定位部分取决于组蛋白上固有 DNA 序列对核小体 DNA 中的 RRRRRYYYYY(R5Y5,R=嘌呤,Y=嘧啶)基序的偏好,该基序是基于 Trifonov 等人的几个理论模型提出的,可能是核小体组装的促进序列模式。然而,没有高一致性的实验证据支持 R5Y5 基序是决定核小体定位的关键因素的概念。在这项工作中,使用盐透析法在体外研究了含有 R5Y5 基序和 TA 重复序列的、具有典型、H2A.Z 和 H3.3 的八聚体在含有这些基序和重复序列的 DNA 模板上组装核小体的能力,这些重复序列的周期性为 10.5bp。结果表明,DNA 模板中 R5Y5 基序和 TA 重复序列的 10.5bp 周期性分布可以显著促进典型核小体的组装,可能是典型核小体组装的关键序列因素。与具有 10.5bp 周期性的 TA 重复序列相比,DNA 模板中的 R5Y5 基序并没有提高 H2A.Z 和 H3.3 含有核小体的体外形成效率。这一结果表明,R5Y5 基序可能不是调节组蛋白变体上核小体组装的关键因素。推测核小体组装的调控机制在典型和变体组蛋白之间是不同的。这些结论可以为核小体定位的机制提供更深入的了解。由 Ramaswamy H. Sarma 交流。

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