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相关概念视频

Nucleosome Remodeling02:54

Nucleosome Remodeling

11.6K
Nucleosomes are the basic units of chromatin compaction. Each nucleosome consists of the DNA bound tightly around a histone core, which makes the DNA inaccessible to DNA binding proteins such as DNA polymerase and RNA polymerase. Hence, the fundamental problem is to ensure access to DNA when appropriate, despite the compact and protective chromatin structure.
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
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Histone Modification02:32

Histone Modification

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The histone proteins have a flexible N-terminal tail extending out from the nucleosome. These histone tails are often subjected to post-translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination. Particular combinations of these modifications form “histone codes” that influence the chromatin folding and tissue-specific gene expression.
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone...
17.0K
The Nucleosome01:19

The Nucleosome

4.7K
Human DNA is almost two meters long. However, it is compressed inside a tiny nucleus measuring only a few microns in diameter. To make this degree of compaction possible, DNA is organized into several sequential levels so that it can fit into such a tiny space. The most compact form of DNA is a chromosome that can be seen under a microscope in a dividing cell.
In a chromosome, DNA is wound twice around a protein complex called a histone octamer core, which consists of 8 histone proteins. This...
4.7K
The Nucleosome02:33

The Nucleosome

19.6K
DNA in a human cell is almost 2m long and it is packed inside a tiny nucleus that is only a few microns in diameter. The level of compaction of DNA inside the nucleus is astonishing. It is organized into several sequentially higher levels of compaction to fit into such a tiny space. The most compact form of DNA is a chromosome that can be seen under a microscope in a dividing cell.
DNA is wound twice around a protein complex called histone core, that consist of 8 histone proteins. This complex...
19.6K
The Nucleosome Core Particle02:10

The Nucleosome Core Particle

15.1K
Nucleosomes are the DNA-histone complex, where the DNA strand is wound around the histone core. The histone core is an octamer containing two copies of H2A, H2B, H3, and H4 histone proteins.
The paradox
Nucleosomes, paradoxically, perform two opposite functions simultaneously. On the one hand, their main responsibility is to protect the delicate DNA strands from physical damage and help achieve a higher compaction ratio. While on the other hand, they must allow polymerase enzymes to access DNA...
15.1K
The Nucleosome Core Particle01:12

The Nucleosome Core Particle

2.6K
Nucleosomes are the DNA-histone complex, where the DNA strand is wound around the histone core. The histone core is an octamer containing two copies of H2A, H2B, H3, and H4 histone proteins.
Nucleosomes, paradoxically, perform two opposite functions simultaneously. On the one hand, their primary aim is to protect the delicate DNA strands from physical damage and help achieve a higher compaction ratio. On the other hand, they must allow polymerase enzymes to access histone-bound DNA during...
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相关实验视频

Updated: Mar 21, 2026

Author Spotlight: Efficient Nucleosome Reconstitution for Single-Molecule Techniques
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Author Spotlight: Efficient Nucleosome Reconstitution for Single-Molecule Techniques

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单分子解码组合修饰核体

Efrat Shema1, Daniel Jones2, Noam Shoresh3

  • 1Department of Pathology and Center for Cancer Research, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA. Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.

Science (New York, N.Y.)
|May 7, 2016
PubMed
概括
此摘要是机器生成的。

新的单分子成像解码核体上的基因组修饰,揭示与细胞活性和表观遗传调节相关的不同状态. 这项技术促进了染色体生物学研究.

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Deciphering Molecular Mechanism of Histone Assembly by DNA Curtain Technique
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Deciphering Molecular Mechanism of Histone Assembly by DNA Curtain Technique

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The ChroP Approach Combines ChIP and Mass Spectrometry to Dissect Locus-specific Proteomic Landscapes of Chromatin
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The ChroP Approach Combines ChIP and Mass Spectrometry to Dissect Locus-specific Proteomic Landscapes of Chromatin

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相关实验视频

Last Updated: Mar 21, 2026

Author Spotlight: Efficient Nucleosome Reconstitution for Single-Molecule Techniques
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Deciphering Molecular Mechanism of Histone Assembly by DNA Curtain Technique
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Deciphering Molecular Mechanism of Histone Assembly by DNA Curtain Technique

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The ChroP Approach Combines ChIP and Mass Spectrometry to Dissect Locus-specific Proteomic Landscapes of Chromatin
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The ChroP Approach Combines ChIP and Mass Spectrometry to Dissect Locus-specific Proteomic Landscapes of Chromatin

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科学领域:

  • 染色体生物学
  • 表观遗传学
  • 分子成像

背景情况:

  • 组合基因修饰调节基因表达,但很难用当前的技术来研究.
  • 了解这些组合状态对于解读表观遗传调节和细胞分化至关重要.

研究的目的:

  • 开发和应用一个高通量单分子成像技术来解码单个核细胞的组合性组合基因组修饰.
  • 调查这些修饰状态如何在多能细胞和遗传细胞之间变化.
  • 评估基因和化学干扰对特定核细胞修饰状态的影响.

主要方法:

  • 高通量单分子核细胞成像.
  • 从干细胞和分化细胞中分析数百万个核细胞.
  • 蛋白质组分析与单分子DNA测序的整合.

主要成果:

  • 双价核体 (抑制和激活标记) 和其他组合状态的识别.
  • 证明这些状态的患病率与发育能力相关.
  • 证据表明染色体酶扰动对具有定义修饰状态的核体产生特定影响.

结论:

  • 开发的单分子成像平台有效地解码组合基因组修饰.
  • 这项技术为细胞发育过程中的表观遗传调节和染色体动力学提供了新的见解.
  • 该平台有很大的潜力解决染色体生物学中的基本问题.