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相关概念视频

Epigenetic Regulation01:46

Epigenetic Regulation

Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
Histone Modification02:32

Histone Modification

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 deacetylase,...
Inheritance of Chromatin Structures03:17

Inheritance of Chromatin Structures

Epigenetics is the study of inherited changes in a cell's phenotype without changing the DNA sequences. It provides a form of memory for the differential gene expression pattern to maintain cell lineage, position-effect variegation, dosage compensation, and maintenance of chromatin structures such as telomeres and centromeres. For example, the structure and location of the centromere on chromosomes are epigenetically inherited. Its functionality is not dictated or ensured by the underlying DNA...
Euchromatin01:01

Euchromatin

The extent of chromatin compaction can be studied by staining chromatin using specific DNA binding dyes. Under the microscope, the dense-compacted regions take up more dye, appearing darker, while the less-compact areas take up less dye and appear lighter. Based on the compaction level, chromatins are classified into two primary forms – euchromatin and heterochromatin.
Euchromatin is the less dense region of the chromatin and stains lighter. Euchromatin contains histone H3 extensively...
Heterochromatin02:38

Heterochromatin

The extent of chromatin compaction can be studied by staining chromatin using specific DNA binding dyes. Under the microscope, the dense-compacted regions that take up more dye are called heterochromatin. Heterochromatin is further classified into two forms – constitutive heterochromatin and facultative heterochromatin.
Constitutive heterochromatin: It is a highly compact region of chromatin that is mostly concentrated in the centromere and telomere. Unlike euchromatin, the amino acid at 9th...
Histone Modification02:32

Histone Modification

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 deacetylase,...

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相关实验视频

Updated: Jun 19, 2026

Combined DNA-RNA Fluorescent In situ Hybridization (FISH) to Study X Chromosome Inactivation in Differentiated Female Mouse Embryonic Stem Cells
15:54

Combined DNA-RNA Fluorescent In situ Hybridization (FISH) to Study X Chromosome Inactivation in Differentiated Female Mouse Embryonic Stem Cells

Published on: June 14, 2014

在Lys-9中素H3的甲基化是X无活化过程中X染色体上的早期标记.

E Heard1, C Rougeulle, D Arnaud

  • 1Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA. edith.heard@curie.fr

Cell
|December 19, 2001
PubMed
概括

基因组H3氨酸9甲基化是X无活化过程中最早发生的染色质变化,发生在XistRNA涂层后. 这种修改有助于在X染色体中传播基因沉默.

科学领域:

  • 表观遗传学和基因调控
  • 染色体生物学 染色体生物学
  • 哺乳动物发展 哺乳动物发展

背景情况:

  • 基因组RNA涂层启动X无活化,但早期的染色质事件仍然不清楚.
  • 了解X失活的初始分子机制对于发育生物学至关重要.
  • 以前的研究集中在转录沉默的后期阶段.

研究的目的:

  • 为了确定XistRNA涂层后最早的染色质重塑事件.
  • 为了研究基因组修饰在X无活化开始过程中的作用.
  • 确定XistRNA结合和表观遗传变化之间的时间关系.

主要方法:

  • 在不活跃的X染色体上分析基因组修饰 (甲基化,乙化).
  • 在XistRNA局部化后立即对基因素标记进行时间分析.
  • 鉴定特定的基因素修饰模式和热点.

主要成果:

  • 基因组H3氨酸9 (H3 Lys-9) 甲基化发生在XistRNA涂层后立即发生,并且在基因沉默之前发生.
  • H3 Lys-9甲基化与H3 Lys-9低乙化和H3 Lys-4低甲基化是一致的.
  • 特定的"热点"H3 Lys-9甲基化被确定为5'到Xist基因位点.

更多相关视频

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images
09:42

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images

Published on: September 7, 2017

Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark
10:09

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

Published on: January 26, 2018

相关实验视频

Last Updated: Jun 19, 2026

Combined DNA-RNA Fluorescent In situ Hybridization (FISH) to Study X Chromosome Inactivation in Differentiated Female Mouse Embryonic Stem Cells
15:54

Combined DNA-RNA Fluorescent In situ Hybridization (FISH) to Study X Chromosome Inactivation in Differentiated Female Mouse Embryonic Stem Cells

Published on: June 14, 2014

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images
09:42

Immunostaining for DNA Modifications: Computational Analysis of Confocal Images

Published on: September 7, 2017

Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark
10:09

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

Published on: January 26, 2018

结论:

  • 基因组H3的修改,特别是H3 Lys-9甲基化,代表了在X无活化过程中最早检测到的染色质变化.
  • 已确定的H3 Lys-9甲基化热点可能作为XistRNA介导的无活化传播的核化地点.
  • 这些发现为引发X染色体沉默的分子级联提供了新的见解.