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相关概念视频

Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

5.8K
DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
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The DNA Replication Fork01:02

The DNA Replication Fork

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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...
35.6K
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

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Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
9.9K
DNA Damage can Stall the Cell Cycle02:37

DNA Damage can Stall the Cell Cycle

9.1K
In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
9.1K
Proofreading01:31

Proofreading

6.2K
Synthesis of new DNA molecules is carried out by the enzyme DNA polymerase, which adds nucleotides on the daughter strand complementary to the template DNA strand. DNA polymerase has a higher affinity to add the correct base and ensures fidelity during DNA replication. Furthermore,  it exhibits proofreading activity during replication, using an exonuclease domain that cuts off incorrect nucleotides from the nascent DNA strand.
Errors During Replication are Corrected by the DNA Polymerase...
6.2K
The Replisome03:01

The Replisome

33.1K
DNA replication is carried out by a large complex of proteins that act in a coordinated matter to achieve high-fidelity DNA replication. Together this complex is known as the DNA replication machinery or the replisome.
The synthesis of the leading and lagging strands is a highly coordinated process. To explain this, the “Trombone model” was proposed by Bruce Alberts in 1980. The DNA loop formation starts when a primer is synthesized on the parent lagging strand. The loop grows with...
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相关实验视频

Updated: Jun 10, 2025

Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
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Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase

Published on: April 29, 2010

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在压力下,DNA聚合酶锁定复制叉.

Xiaomeng Jia1,2, James T Inman1,2, Anupam Singh3

  • 1Howard Hughes Medical Institute, Cornell University, Ithaca, NY 14853, USA.

bioRxiv : the preprint server for biology
|October 17, 2024
PubMed
概括
此摘要是机器生成的。

DNA聚合酶 (DNAP) 在对抗复制叉压力时禁用DNA复制. 这就是DNAP DNAP.

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Inducing a Site Specific Replication Blockage in E. coli Using a Fluorescent Repressor Operator System
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Inducing a Site Specific Replication Blockage in E. coli Using a Fluorescent Repressor Operator System

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Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes
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Last Updated: Jun 10, 2025

Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
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Inducing a Site Specific Replication Blockage in E. coli Using a Fluorescent Repressor Operator System
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Inducing a Site Specific Replication Blockage in E. coli Using a Fluorescent Repressor Operator System

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Single-Molecule Fluorescence Visualization of DNA Polymerase Dynamics at G-Quadruplexes
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科学领域:

  • 分子生物学分子生物学
  • 生物化学 生物化学
  • 遗传学 遗传学 是一个

背景情况:

  • DNA复制需要通过复制体解开父母DNA.
  • DNA聚合酶 (DNAP) 和螺旋酶是复原体中的关键蛋白质.
  • DNAP独立于螺旋酶运作的后果尚未完全理解.

研究的目的:

  • 为了研究DNAP在复制叉应力下运行的效应.
  • 了解DNAP与复制叉之间的相互作用.
  • 阐明在压力过程中保护复制叉的机制.

主要方法:

  • 在模拟复制叉压力下检查DNAP行为.
  • 分析了DNAP与领先和滞后DNA链的相互作用.
  • 研究了DNAP外核酶活性在叉子稳定性中的作用.

主要成果:

  • 长时间暴露在叉式压力下的DNAP会导致复制失活.
  • DNAP与DNA链强烈相互作用,导致复制叉锁定.
  • DNAP的逆转移 (外核酶活性) 对于防止分叉失活至关重要.
  • 添加酸酶不能逆转观察到的叉锁.

结论:

  • 在压力下,DNAP与复制叉的相互作用会导致叉锁和失活.
  • 在压力期间,DNAP外核酶活动对于维持复制叉活动至关重要.
  • 了解DNAP分叉动态是理解复制应激反应的关键.