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相关概念视频

Histone Modification02:32

Histone Modification

13.4K
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...
13.4K
Epigenetic Regulation01:37

Epigenetic Regulation

3.1K
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...
3.1K
Lysosomal Hydrolases01:22

Lysosomal Hydrolases

3.8K
Lysosomes are the site for the degradation of macromolecules and biological polymers released during membrane trafficking events such as secretory, endocytic, autophagic, and phagocytic pathways. The membrane-enclosed area of the lysosome, called the lumen, contains hydrolytic enzymes active in an acidic environment. These acid hydrolases are functional at a pH between 4.5 and 5 and are involved in cellular processes such as cell signaling, energy metabolism, restoration of the plasma membrane,...
3.8K
Spreading of Chromatin Modifications02:25

Spreading of Chromatin Modifications

8.3K
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...
8.3K
Lysogenic Cycle of Bacteriophages00:43

Lysogenic Cycle of Bacteriophages

62.3K
In contrast to the lytic cycle, phages infecting bacteria via the lysogenic cycle do not immediately kill their host cell. Instead, they combine their genome with the host genome, allowing the bacteria to replicate the phage DNA along with the bacterial genome. The incorporated copy of the phage genome is called the prophage. Some prophages can re-activate and enter the lytic cycle. This often occurs in response to a perturbation, such as DNA damage, but can also transpire in the absence of...
62.3K
Viral Replication: Lysogenic Cycle01:16

Viral Replication: Lysogenic Cycle

43
The lysogenic cycle is a crucial viral replication strategy that allows bacteriophages to persist within host cells without immediately destroying them. This process is primarily observed in temperate phages, such as bacteriophage lambda (λ), which infects Escherichia coli. The cycle allows the viral genome to persist across bacterial generations while keeping host cells viable.Integration of the Viral GenomeUpon infection, bacteriophage lambda attaches to the bacterial surface and injects...
43

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相关实验视频

Updated: Jul 15, 2025

Application of MassSQUIRM for Quantitative Measurements of Lysine Demethylase Activity
07:02

Application of MassSQUIRM for Quantitative Measurements of Lysine Demethylase Activity

Published on: March 11, 2012

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lysine 脱甲基化在病变发生过程中的作用

Jian Cao1,2, Qin Yan3

  • 1Rutgers Cancer Institute of New Jersey, New Brunswick, NJ, 08901, USA. jian.cao@rutgers.edu.

Advances in experimental medicine and biology
|September 26, 2023
PubMed
概括

基因组脱甲基酶调节基因表达,在发育和疾病中至关重要. 向这些酶的抑制剂在治疗癌症和其他疾病方面表现有前途.

关键词:
氨基氧化酶的氨基氧化酶是什么癌症 癌症 癌症 癌症希斯脱甲基酶 (Histone Demethylase) 是一种酶.希斯甲基化 希斯甲基化氧化酶是一种氧化酶.在JmjCC中,我们在KDM中,KDM就是KDM.这是一种KDM抑制剂.一个LSD1一个LSD1氨酸脱甲基酶是一种氨酸脱甲基酶.

更多相关视频

Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark
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Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark

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Specificity Analysis of Protein Lysine Methyltransferases Using SPOT Peptide Arrays
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Specificity Analysis of Protein Lysine Methyltransferases Using SPOT Peptide Arrays

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相关实验视频

Last Updated: Jul 15, 2025

Application of MassSQUIRM for Quantitative Measurements of Lysine Demethylase Activity
07:02

Application of MassSQUIRM for Quantitative Measurements of Lysine Demethylase Activity

Published on: March 11, 2012

13.4K
Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark
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Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark

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Specificity Analysis of Protein Lysine Methyltransferases Using SPOT Peptide Arrays
08:48

Specificity Analysis of Protein Lysine Methyltransferases Using SPOT Peptide Arrays

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科学领域:

  • 生物化学 生物化学
  • 分子生物学分子生物学
  • 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.

背景情况:

  • 基因组甲基化是调节基因表达,DNA修复和发育的关键表观遗传机制.
  • 基因组 lysine 脱甲基酶 (KDMs) 逆转基因组甲基化,在细胞过程中发挥关键作用.
  • KDMs的失调与各种人类疾病有关,特别是癌症.

研究的目的:

  • 总结基因组脱甲基酶在正常发育和疾病中的作用.
  • 审查针对KDM治疗疾病的治疗策略.

主要方法:

  • 关于基因组脱甲基酶的研究的文献综述.
  • 分析KDM抑制剂的发展和临床进展.

主要成果:

  • 自2004年发现LSD1/KDM1A以来,已经确定并描述了八个KDM亚家族.
  • 针对KDM的小分子抑制剂已经通过学术和工业合作开发出来.
  • 几种KDM抑制剂已经进入癌症和其他疾病的临床试验.

结论:

  • 基因组脱甲基酶是重要的表观遗传调节剂,在健康和疾病中起着重要作用.
  • 用小分子抑制剂向KDM代表了对包括癌症在内的各种疾病的有希望的治疗途径.