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表观遗传学的物理化学:单分子研究。

Physical Chemistry of Epigenetics: Single-Molecule Investigations.

机构信息

Department of Chemistry , The Pennsylvania State University , University Park 16803 , Pennsylvania , United States.

出版信息

J Phys Chem B. 2019 Oct 10;123(40):8351-8362. doi: 10.1021/acs.jpcb.9b06214. Epub 2019 Aug 30.

DOI:10.1021/acs.jpcb.9b06214
PMID:31404497
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6790939/
Abstract

The nucleosome is the fundamental building block of the eukaryotic genome, composed of an ∼147 base-pair DNA fragment wrapping around an octameric histone protein core. DNA and histone proteins are targets of enzymatic chemical modifications that serve as signals for gene regulation. These modifications are often referred to as epigenetic modifications that govern gene activities without altering the DNA sequence. Although the term epigenetics initially required inheritability, it now frequently includes noninherited histone modifications associated with gene regulation. Important epigenetic modifications for healthy cell growth and proliferation include DNA methylation, histone acetylation, methylation, phosphorylation, ubiquitination, and SUMOylation (SUMO = Small Ubiquitin-like Modifier). Our research focuses on the biophysical roles of these modifications in altering the structure and structural dynamics of the nucleosome and their implications in gene regulation mechanisms. As the changes are subtle and complex, we employ various single-molecule fluorescence approaches for their investigations. Our investigations revealed that these modifications induce changes in the structure and structural dynamics of the nucleosome and their thermodynamic and kinetic stabilities. We also suggested the implications of these changes in gene regulation mechanisms that are the foci of our current and future research.

摘要

核小体是真核基因组的基本构建块,由一个约 147 个碱基对的 DNA 片段缠绕在一个八聚体组蛋白核心周围。DNA 和组蛋白是酶化学修饰的靶标,这些修饰作为基因调控的信号。这些修饰通常被称为表观遗传修饰,它们可以在不改变 DNA 序列的情况下控制基因活性。尽管表观遗传学这个术语最初需要可遗传性,但现在它通常包括与基因调控相关的非遗传性组蛋白修饰。对于健康细胞生长和增殖的重要表观遗传修饰包括 DNA 甲基化、组蛋白乙酰化、甲基化、磷酸化、泛素化和 SUMO 化(SUMO=Small Ubiquitin-like Modifier)。我们的研究重点是这些修饰在改变核小体结构和结构动力学方面的生物物理作用及其在基因调控机制中的意义。由于这些变化细微而复杂,我们采用了各种单分子荧光方法进行研究。我们的研究表明,这些修饰会导致核小体结构和结构动力学以及热力学和动力学稳定性的变化。我们还提出了这些变化在基因调控机制中的意义,这是我们当前和未来研究的重点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e7/6790939/355db648db2c/jp9b06214_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e7/6790939/a60c8516e01d/jp9b06214_0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e7/6790939/355db648db2c/jp9b06214_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e7/6790939/a60c8516e01d/jp9b06214_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e7/6790939/6f0fb1c00f20/jp9b06214_0002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e7/6790939/1870c86141fe/jp9b06214_0006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45e7/6790939/355db648db2c/jp9b06214_0008.jpg

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2
Single-molecule FRET method to investigate the dynamics of transcription elongation through the nucleosome by RNA polymerase II.利用单分子 FRET 方法研究 RNA 聚合酶 II 通过核小体转录延伸的动力学。
Methods. 2019 Apr 15;159-160:51-58. doi: 10.1016/j.ymeth.2019.01.009. Epub 2019 Jan 17.
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Structure of an H1-Bound 6-Nucleosome Array Reveals an Untwisted Two-Start Chromatin Fiber Conformation.
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Histone variants H3.3 and H2A.Z/H3.3 facilitate excision of uracil from nucleosome core particles.组蛋白变体 H3.3 和 H2A.Z/H3.3 有助于从核小体核心颗粒中切除尿嘧啶。
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