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相关概念视频

Conserved Binding Sites01:49

Conserved Binding Sites

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Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
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DNA as a Genetic Template02:05

DNA as a Genetic Template

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Two structural features of the DNA molecule provide a basis for the mechanisms of heredity: the four nucleotide bases and its double-stranded nature. The Watson-Crick model of double-helical DNA structure, proposed in 1952, drew heavily upon the X-ray crystallography work of researchers Rosalind Franklin and Maurice Wilkins. Watson, Crick, and Wilkins jointly received the Nobel Prize in Physiology or Medicine for their work in 1962. Franklin was, controversially, excluded from the prize for...
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Cooperative Binding of Transcription Regulators02:13

Cooperative Binding of Transcription Regulators

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Transcriptional regulators bind to specific cis-regulatory sequences in the DNA to regulate gene transcription. These cis-regulatory sequences are very short, usually less than ten nucleotide pairs in length. The short length means that there is a high probability of the exact same sequence randomly occurring throughout the genome.  Since regulators can also bind to groups of similar sequences, this further increases the chances of random binding. Transcriptional regulators form...
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Cooperative Binding of Transcription Regulators02:13

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Heterochromatin02:38

Heterochromatin

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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.
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Cis-regulatory Sequences02:02

Cis-regulatory Sequences

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Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
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相关实验视频

Updated: Apr 5, 2026

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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一个用于3D基因组结构的CTCF代码

Michael H Nichols1, Victor G Corces1

  • 1Department of Biology, Emory University, 1510 Clifton Road NE, Atlanta, GA 30322, USA.

Cell
|August 16, 2015
PubMed
概括
此摘要是机器生成的。

结构蛋白CTCF结合点的方向决定了基因组的3D组织. CTCF位点定向作为一个代码,限制相互作用并预测DNA循环的形成.

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Deciphering High-Resolution 3D Chromatin Organization via Capture Hi-C
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Deciphering High-Resolution 3D Chromatin Organization via Capture Hi-C

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HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries
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HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries

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相关实验视频

Last Updated: Apr 5, 2026

Hi-C: A Method to Study the Three-dimensional Architecture of Genomes.
22:27

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

Published on: May 6, 2010

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Deciphering High-Resolution 3D Chromatin Organization via Capture Hi-C
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Deciphering High-Resolution 3D Chromatin Organization via Capture Hi-C

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HOX Loci Focused CRISPR/sgRNA Library Screening Identifying Critical CTCF Boundaries
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科学领域:

  • 基因组学
  • 分子生物学
  • 表观遗传学

背景情况:

  • 结构蛋白CTCF对于基因组调节至关重要.
  • 了解三维基因组结构是解码基因功能的关键.

研究的目的:

  • 调查CTCF位点定向如何影响基因组3D组织.
  • 根据CTCF确定基因组折叠的预测代码.
  • 提出一个CTCF介导的DNA循环形成模型.

主要方法:

  • 对CTCF结合点方向的分析
  • 全基因组互动映射
  • 对DNA循环的生物物理模型的开发.

主要成果:

  • CTCF位点定向显著限制了DNA交互伙伴.
  • 一个基于CTCF定向的代码预测了基因组折叠模式.
  • 定向特异性的循环形成是由DNA挤出模型解释的.

结论:

  • CTCF定向是3D基因组架构的一个关键决定因素.
  • 提出的DNA挤出模型解释了取决于方向的基因组循环.
  • 这项工作为了解基因组组织提供了一个新的框架.