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相关概念视频

Replication in Eukaryotes01:29

Replication in Eukaryotes

14.8K
In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before cell division, so there are many proteins that fulfill specialized roles in the replication process. Replication occurs in three phases: initiation, elongation, and termination, and ends with two complete sets of chromosomes in the nucleus.
Many Proteins Orchestrate Replication at the Origin
Eukaryotic replication follows many of the same...
14.8K
Chromosome Replication02:31

Chromosome Replication

9.1K
Before a cell can divide, it must accurately replicate all of its chromosomes, including the DNA and its associated histone and non-histone proteins.  This process begins at numerous origins of replication during the S phase of the cell cycle in each of a cell’s chromosomes simultaneously. Certain nucleotides can act as origins of replication, but these sequences are not well defined - especially in complex, multi-cellular, eukaryotic species. The length of DNA that spans an origin...
9.1K
The DNA Replication Fork01:02

The DNA Replication Fork

36.9K
An organism’s genome needs to be duplicated in an efficient and error-free manner for its growth and survival. The replication fork is a Y-shaped active region where two strands of DNA are separated and replicated continuously. The coupling of DNA unzipping and complementary strand synthesis is a characteristic feature of a replication fork.   Organisms with small circular DNA, such as E. coli, often have a single origin of replication; therefore, they have only two replication...
36.9K
Replication in Prokaryotes01:32

Replication in Prokaryotes

25.4K
DNA replication has three main steps: initiation, elongation, and termination. Replication in prokaryotes begins when initiator proteins bind to the single origin of replication (ori) on the cell's circular chromosome. Replication then proceeds around the entire circle of the chromosome in each direction from the two replication forks, resulting in two DNA molecules.
Many Proteins Work Together to Replicate the Chromosome
Replication is coordinated and carried out by a host of specialized...
25.4K
Duplication of Chromatin Structure02:05

Duplication of Chromatin Structure

6.0K
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...
6.0K
DNA Replication02:40

DNA Replication

51.1K
DNA replication involves the separation of the two strands of the double helix, with each strand serving as a template from which the new complementary strand is copied.  After replication, each double-stranded DNA includes one parental or “old” strand and one “new” strand. This is known as semiconservative replication. The resulting DNA molecules have the same sequence and are divided equally into the two daughter cells.
Replication in Prokaryotes
DNA replication...
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相关实验视频

Updated: Sep 19, 2025

Imaging Replicative Domains in Ultrastructurally Preserved Chromatin by Electron Tomography
14:56

Imaging Replicative Domains in Ultrastructurally Preserved Chromatin by Electron Tomography

Published on: May 20, 2022

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不平衡复制过程产生了染色质折叠的初始模板.

Kiran Kumari1

  • 1Indian Institute of Technology Bombay, Department of Biosciences and Bioengineering, Mumbai, Maharashtra 400076, India.

Physical review. E
|June 19, 2025
PubMed
概括
此摘要是机器生成的。

这项研究探讨了DNA如何复制和染色质如何在复制后重新折叠. 复制分叉速度显著影响新合成的染色质组织,影响欧克罗马丁和异性染色质的形成.

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A Method to Study de novo Formation of Chromatin Domains
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A Method to Study de novo Formation of Chromatin Domains

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Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method
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相关实验视频

Last Updated: Sep 19, 2025

Imaging Replicative Domains in Ultrastructurally Preserved Chromatin by Electron Tomography
14:56

Imaging Replicative Domains in Ultrastructurally Preserved Chromatin by Electron Tomography

Published on: May 20, 2022

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A Method to Study de novo Formation of Chromatin Domains
07:34

A Method to Study de novo Formation of Chromatin Domains

Published on: August 23, 2019

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Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method
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Strand-Specific Analysis of Proteins at Replicating DNA Strands by Enrichment and Sequencing of Protein-Associated Nascent DNA Method

Published on: May 2, 2025

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科学领域:

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

背景情况:

  • DNA复制对于细胞分裂至关重要,但在这个过程中表观遗传信息的保存尚不清楚.
  • 在基因组复制后,染色体必须重新折叠成其3D结构.
  • 复制发生在时间调节的领域,具有启动模式.

研究的目的:

  • 研究DNA复制后立即发生的3D染色质折叠的不平衡过程.
  • 确定在复制和重新折叠期间表观遗传信息是如何保持的.
  • 分析复制动力学对复制后染色质结构的影响.

主要方法:

  • 利用随机模拟方法来建模染色体折叠.
  • 为特定的复制域生成了接触概率图.
  • 研究了复制起源位置和分叉速度的影响.

主要成果:

  • 复制后的染色质结构受到复制起源位置和复制的非平衡性质的影响.
  • 复制分叉速度显著影响新合成的染色质的组织.
  • 复制分叉速度会影响接触密度和形成类似于欧克罗马和类似于 heterochromatin 的结构.

结论:

  • DNA复制的动态,特别是分叉速度,在建立复制后的染色质组织方面发挥着至关重要的作用.
  • 了解这些不平衡过程是理解细胞分裂期间表观遗传记忆的关键.
  • 这项工作提供了关于染色体在复制后如何实现特定结构的见解.