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相关概念视频

Nucleosome Remodeling02:54

Nucleosome Remodeling

8.8K
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...
8.8K
The Nucleosome01:19

The Nucleosome

1.2K
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...
1.2K
Genomic DNA in Eukaryotes00:58

Genomic DNA in Eukaryotes

46.5K
Eukaryotes have large genomes compared to prokaryotes. To fit their genomes into a cell, eukaryotic DNA is packaged extraordinarily tightly inside the nucleus. To achieve this, DNA is tightly wound around proteins called histones, which are packaged into nucleosomes that are joined by linker DNA and coil into chromatin fibers. Additional fibrous proteins further compact the chromatin, which is recognizable as chromosomes during certain phases of cell division.
46.5K
Chromatin Packaging01:32

Chromatin Packaging

16.5K
Each human somatic cell contains 6 billion base pairs of DNA. Each base pair is 0.34 nm long, meaning each diploid cell contains a staggering 2 meters of DNA. This long DNA strand is packed inside a nucleus measuring only 10-20 microns in diameter with the help of specialized DNA-binding proteins called histones. Together they form a compact DNA-protein complex called chromatin. The chromatin is further compacted into higher-order structures. The highest level of compaction is achieved during...
16.5K
Duplication of Chromatin Structure02:05

Duplication of Chromatin Structure

5.2K
The process of chromosome duplication during cell division requires genome-wide disruption and re-assembly of chromatin. The chromatin structure must be accurately inherited, reassembled, and maintained in the daughter cells to ensure lineage propagation.
The basic unit of the chromatin is the nucleosome, consisting of DNA wrapped around octameric histone proteins and short stretches of linker DNA separating individual nucleosomes. The histone proteins within the nucleosome have their...
5.2K
Inheritance of Chromatin Structures03:17

Inheritance of Chromatin Structures

6.2K
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...
6.2K

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相关实验视频

Updated: May 12, 2025

3D Multicolor DNA FISH Tool to Study Nuclear Architecture in Human Primary Cells
11:25

3D Multicolor DNA FISH Tool to Study Nuclear Architecture in Human Primary Cells

Published on: January 25, 2020

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为了解码塑造亚兆基基基基因组组织的机制.

Joseph M Paggi1, Bin Zhang1

  • 1Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, 02139, MA, USA.

Current opinion in structural biology
|May 9, 2025
PubMed
概括

基因组组织理论正在进步,解释了新的结构,如微分区和微域. 新模型整合了各种数据,揭示了分子力量如何塑造染色质结构和调节转录.

科学领域:

  • 基因组学就是基因组学.
  • 分子生物学分子生物学
  • 生物物理学的生物物理.

背景情况:

  • 基因组组织在千基-兆基尺度对基因调节至关重要.
  • 最近的技术揭示了新的结构图案,如微分区和核细胞离合体.
  • 现有的理论很难完全解释这些复杂的结构.

研究的目的:

  • 审查最近在理解基因组组织方面的理论进展.
  • 阐明观察到的染色体结构背后的机制.
  • 探索分子力量如何集体调节转录.

主要方法:

  • 审查最近的理论和实验进步.
  • 核细胞定位和表观遗传修饰的分析.
  • 将染色体构造捕获数据与基因组学数据集集的整合.
  • 开发类似原生染色体模型.

主要成果:

  • 阐明了核细胞定位,表观遗传修饰和细分的作用.
  • 了解循环挤出和相位分离之间的相互作用.
  • 对新出现的色素结构的可能机制的识别.

结论:

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Promoter Capture Hi-C: High-resolution, Genome-wide Profiling of Promoter Interactions

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Hi-C: A Method to Study the Three-dimensional Architecture of Genomes.
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Hi-C: A Method to Study the Three-dimensional Architecture of Genomes.

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3D Multicolor DNA FISH Tool to Study Nuclear Architecture in Human Primary Cells

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Promoter Capture Hi-C: High-resolution, Genome-wide Profiling of Promoter Interactions
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Promoter Capture Hi-C: High-resolution, Genome-wide Profiling of Promoter Interactions

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Hi-C: A Method to Study the Three-dimensional Architecture of Genomes.
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Hi-C: A Method to Study the Three-dimensional Architecture of Genomes.

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  • 在解释色素结构方面取得了重大进展.
  • 在细胞环境中各种因素的综合作用仍然是一个开放的问题.
  • 先进的建模策略有望解码染色体结构功能关系.