中心粒核小体的纳米级结构、相互作用和动力学。

IF 5.4 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
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引用次数: 0

摘要

中心粒是染色体的特定区段,由两种类型的核小体组成:一种是含有 H2A、H2B、H3 和 H4 组蛋白八聚体的标准核小体;另一种是用类似物 CENP-A 代替 H3 的 CENP-A 核小体。这种修饰导致了 DNA 包膜的差异(121 bp),大大小于标准核小体的 147 bp。我们使用原子力显微镜(AFM)和高速原子力显微镜(HS-AFM)来描述这两种核小体的纳米级特征和动力学特性。对于这两种核小体,我们都观察到了DNA的自发非对称解开,这一过程是通过一个瞬时状态发生的,即DNA在核心周围缠绕了100 bp,随后DNA迅速解离。此外,HS-AFM显示,与H3核小体相比,CENP-A核小体的稳定性更高,在H3核小体中,组蛋白核心解离发生在核小体解离之前。这些结果有助于阐明这些核小体之间的差异以及 CENP-A 核小体的潜在生物学必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Nanoscale Structure, Interactions, and Dynamics of Centromere Nucleosomes

Nanoscale Structure, Interactions, and Dynamics of Centromere Nucleosomes

Centromeres are specific segments of chromosomes comprising two types of nucleosomes: canonical nucleosomes containing an octamer of H2A, H2B, H3, and H4 histones and CENP-A nucleosomes in which H3 is replaced with its analogue CENP-A. This modification leads to a difference in DNA wrapping (∼121 bp), considerably less than 147 bp in canonical nucleosomes. We used atomic force microscopy (AFM) and high-speed AFM (HS-AFM) to characterize nanoscale features and dynamics for both types of nucleosomes. For both nucleosomes, spontaneous asymmetric unwrapping of DNA was observed, and this process occurs via a transient state with ∼100 bp DNA wrapped around the core, followed by a rapid dissociation of DNA. Additionally, HS-AFM revealed higher stability of CENP-A nucleosomes compared with H3 nucleosomes in which dissociation of the histone core occurs prior to the nucleosome dissociation. These results help elucidate the differences between these nucleosomes and the potential biological necessity for CENP-A nucleosomes.

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来源期刊
Biomacromolecules
Biomacromolecules 化学-高分子科学
CiteScore
10.60
自引率
4.80%
发文量
417
审稿时长
1.6 months
期刊介绍: Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine. Topics covered by Biomacromolecules include, but are not exclusively limited to: sustainable polymers, polymers based on natural and renewable resources, degradable polymers, polymer conjugates, polymeric drugs, polymers in biocatalysis, biomacromolecular assembly, biomimetic polymers, polymer-biomineral hybrids, biomimetic-polymer processing, polymer recycling, bioactive polymer surfaces, original polymer design for biomedical applications such as immunotherapy, drug delivery, gene delivery, antimicrobial applications, diagnostic imaging and biosensing, polymers in tissue engineering and regenerative medicine, polymeric scaffolds and hydrogels for cell culture and delivery.
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