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相关概念视频

Histone Modification02:32

Histone Modification

15.9K
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...
15.9K
Histone Modification02:32

Histone Modification

4.4K
4.4K
Spreading of Chromatin Modifications02:25

Spreading of Chromatin Modifications

9.3K
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...
9.3K
Covalently Linked Protein Regulators02:04

Covalently Linked Protein Regulators

8.6K
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....
8.6K
The Nucleosome Core Particle01:12

The Nucleosome Core Particle

2.1K
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.
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...
2.1K
The Nucleosome Core Particle02:10

The Nucleosome Core Particle

14.1K
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...
14.1K

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相关实验视频

Updated: Jan 12, 2026

Complete Workflow for Analysis of Histone Post-translational Modifications Using Bottom-up Mass Spectrometry: From Histone Extraction to Data Analysis
11:02

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

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历史代码 (HistENCODE):一个拟议的项目,用于解读基因组 PTM 之间和基因组 PTM 之间的功能相互作用.

A Gregory Matera1

  • 1Integrative Program for Biological and Genome Sciences, Departments of Biology and Genetics, University of North Carolina, Chapel Hill, NC 27599-7100, USA.

Trends in genetics : TIG
|November 5, 2025
PubMed
概括

希斯顿代码假设需要进一步调查25年后. 一项名为HISTENCODE的新计划将利用突变发生来绘制基因组转化后修饰 (PTMs) 和它们在基因调节中的作用.

科学领域:

  • 表观遗传学和基因调控
  • 分子生物学分子生物学
  • 基因组学就是基因组学.

背景情况:

  • 25年前提出的基因组编码假设表明,基因组后翻译修饰 (PTMs) 的组合调节基因表达.
  • 尽管具有重要意义,但关于基因素PTM之间的确切功能关系的基本问题仍然没有得到解决.

研究的目的:

  • 为了解决围绕着基质子代码假设的未解决的问题.
  • 提出和概述一个多实验室倡议,HISTENCODE,用于系统的调查.
  • 解读基因组 PTM 之间的功能关系及其对基因调节的影响.

主要方法:

  • 基因素N终端尾部残留物的直接突变发生.
  • 系统地检查了基因素PTMs.
  • 多实验室的协作方法.

主要成果:

  • 本部分概述的是拟议的倡议,而不是实验结果.
  • 该倡议旨在系统地绘制基因组PTM之间的功能关系.

结论:

  • 需要一个协调一致的,多实验室的努力,才能充分理解基质子代码.

更多相关视频

Global Level Quantification of Histone Post-Translational Modifications in a 3D Cell Culture Model of Hepatic Tissue
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Global Level Quantification of Histone Post-Translational Modifications in a 3D Cell Culture Model of Hepatic Tissue

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Author Spotlight: Enhanced Histone PTM Isomer Identification Through LC-TIMS-ToF MS/MS and PASEF
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Author Spotlight: Enhanced Histone PTM Isomer Identification Through LC-TIMS-ToF MS/MS and PASEF

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相关实验视频

Last Updated: Jan 12, 2026

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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Global Level Quantification of Histone Post-Translational Modifications in a 3D Cell Culture Model of Hepatic Tissue
08:12

Global Level Quantification of Histone Post-Translational Modifications in a 3D Cell Culture Model of Hepatic Tissue

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Author Spotlight: Enhanced Histone PTM Isomer Identification Through LC-TIMS-ToF MS/MS and PASEF
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Author Spotlight: Enhanced Histone PTM Isomer Identification Through LC-TIMS-ToF MS/MS and PASEF

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  • 拟议的HISTENCODE倡议将提供一个系统的框架来破译质子PTM功能.
  • 解读这些关系对于推进我们对基因调节的理解至关重要.