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相关概念视频

Histone Modification02:32

Histone Modification

13.1K
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...
13.1K
Spreading of Chromatin Modifications02:25

Spreading of Chromatin Modifications

8.2K
The histone proteins in the nucleosomes are post-translationally modified (PTM) to increase or decrease access to DNA. The commonly observed PTMs are methylation, acetylation, phosphorylation, and ubiquitination of lysine amino acids in the histone H3 tail region. These histone modifications have specific meaning for the cell. Hence, they are called "histone code". The protein complex involved in histone modification is termed as "reader-writer" complex.
Writers
The writer...
8.2K
Covalently Linked Protein Regulators02:04

Covalently Linked Protein Regulators

6.8K
Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein....
6.8K
Epigenetic Regulation01:37

Epigenetic Regulation

3.0K
Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
3.0K
RNA Stability01:53

RNA Stability

33.3K
Intact DNA strands can be found in fossils, while scientists sometimes struggle to keep RNA intact under laboratory conditions. The structural variations between RNA and DNA underlie the differences in their stability and longevity. Because DNA is double-stranded, it is inherently more stable. The single-stranded structure of RNA is less stable but also more flexible and can form weak internal bonds. Additionally, most RNAs in the cell are relatively short, while DNA can be up to 250 million...
33.3K
The Nucleosome Core Particle01:12

The Nucleosome Core Particle

884
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...
884

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相关实验视频

Updated: Jun 10, 2025

Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark
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由蛋白质稳定性控制的基氨酸甲基化修饰剂.

Sungryul Park1, Jin Hwa Cho1, Jeong-Hoon Kim2,3

  • 1Disease Target Structure Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.

Experimental & molecular medicine
|October 11, 2024
PubMed
概括

蛋白质降解控制着基因组 lysine 的甲基化,影响细胞功能和人类疾病. 准修饰蛋白稳定性为表观遗传调节提供了新的治疗策略.

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Complete Workflow for Analysis of Histone Post-translational Modifications Using Bottom-up Mass Spectrometry: From Histone Extraction to Data Analysis
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Complete Workflow for Analysis of Histone Post-translational Modifications Using Bottom-up Mass Spectrometry: From Histone Extraction to Data Analysis
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科学领域:

  • 表观遗传学和分子生物学
  • 细胞调节和疾病机制.

背景情况:

  • 基因组 lysine 甲基化对于表观遗传调节至关重要,它影响着 DNA 模板化的过程.
  • 基因组甲基化修饰剂 (甲基转移酶和脱甲基酶) 的活性取决于它们的蛋白质稳定性,这种稳定性由降解来调节.
  • 动态表观遗传变化是由这些修饰物的协调作用调节的.

研究的目的:

  • 通过表观遗传变化,回顾当前对蛋白质降解如何影响细胞生理学的理解.
  • 总结异常修饰蛋白稳定性和人类疾病之间的联系.
  • 突出治疗潜力,针对新型治疗策略的蛋白质稳定性.

主要方法:

  • 对影响基因组修饰剂的蛋白质降解途径现有研究的文献综述.
  • 修饰蛋白稳定性与表观遗传变化之间的功能联系的分析.
  • 检查疾病关联和治疗向蛋白质稳定性的研究.

主要成果:

  • 蛋白质降解途径极为关键地调节 histone lysine 甲基化修饰剂的稳定性和活性.
  • 这些修饰剂的稳定性变化导致显著的表观遗传变化,影响基本的细胞过程.
  • 修饰蛋白稳定性的失调与各种人类疾病有关.

结论:

  • 了解修饰蛋白降解是理解表观遗传调节和细胞生理学的关键.
  • 准蛋白质稳定性为开发针对表观遗传相关疾病的新治疗策略提供了有希望的途径.