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相关概念视频

The DNA Replication Fork01:02

The DNA Replication Fork

40.3K
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...
40.3K
The DNA Replication Fork01:02

The DNA Replication Fork

18.0K
18.0K
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

6.2K
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,...
6.2K
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

2.3K
2.3K
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

11.0K
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...
11.0K
Homologous Recombination02:31

Homologous Recombination

62.5K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
62.5K

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相关实验视频

Updated: Jan 10, 2026

Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
07:27

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

Published on: April 29, 2010

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转录复制碰撞触发了高保真复制重置.

Matthew B Cooke1, Kobie T Welch1, Laura Deus Ramirez1

  • 1Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, United States.

Nucleic acids research
|November 26, 2025
PubMed
概括
此摘要是机器生成的。

翻译-转录脱导致DNA通过转录-复制碰撞 (TRC) 断裂. 一种新的"复制重置"机制解决了这些DNA末端,保持了基因组的稳定性,而不会引发损伤反应.

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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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Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization
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Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization

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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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Chromosome Replicating Timing Combined with Fluorescent In situ Hybridization
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科学领域:

  • 微生物学 微生物学
  • 分子生物学分子生物学
  • 遗传学 是一个遗传学.

背景情况:

  • 双链DNA末端对基因组的稳定性构成威胁.
  • 转录复制碰撞 (TRCs) 是已知的DNA损伤的来源.

研究的目的:

  • 为了确定参与大肠杆菌中DNA末端形成的因素.
  • 阐明TRCs导致DNA末端形成和分辨的机制.

主要方法:

  • 基因组CRISPRi屏幕被用于识别DNA末端形成因素.
  • 研究了RecBCD和重组途径在DNA终端处理中的作用.

主要成果:

  • 发现翻译-转录脱会通过TRC依赖的途径导致DNA末端的形成.
  • TRCs导致复杂体停滞和随后的DNA末端生成,而不是链断裂.
  • 一个称为"复制重置"的新过程通过复制核降解来解决这些DNA末端,避免重组,DNA损伤反应或突变发生.

结论:

  • 一种新的DNA保护机制,即"复制重置",在复制压力期间保持基因组稳定性.
  • 挑战了TRCs总是导致细菌基因组不稳定的假设.