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相关概念视频

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...
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Homologous Recombination02:31

Homologous Recombination

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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...
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Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

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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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Lagging Strand Synthesis01:59

Lagging Strand Synthesis

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During replication, the complementary strands in double-stranded DNA are synthesized at different rates. Replication first begins on the leading strand. Replication starts later, occurs more slowly, and proceeds discontinuously on the lagging strand.
There are several major differences between synthesis of the leading strand and synthesis of the lagging strand. 1) Leading strand synthesis happens in the direction of replication fork opening, whereas lagging strand synthesis happens in the...
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Mismatch Repair01:20

Mismatch Repair

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Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
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The Replisome03:01

The Replisome

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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: Aug 16, 2025

Design and Synthesis of a Reconfigurable DNA Accordion Rack
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Design and Synthesis of a Reconfigurable DNA Accordion Rack

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在随机序列池中以指针为媒介的线程移位

Thomas Mayer1, Lukas Oesinghaus1, Friedrich C Simmel1

  • 1School of Natural Sciences, Department of Bioscience, TU Munich, D-85748Garching, Germany.

Journal of the American Chemical Society
|December 26, 2022
PubMed
概括
此摘要是机器生成的。

了解DNA序列背景对于强大的分子电路至关重要. 这项研究揭示了一些强烈交互的序列主导电路动力学,即使在复杂的环境中也能实现可预测的电路设计.

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A Simple, Robust, and High Throughput Single Molecule Flow Stretching Assay Implementation for Studying Transport of Molecules Along DNA
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A Simple, Robust, and High Throughput Single Molecule Flow Stretching Assay Implementation for Studying Transport of Molecules Along DNA

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Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51
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Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51

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相关实验视频

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Design and Synthesis of a Reconfigurable DNA Accordion Rack
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A Simple, Robust, and High Throughput Single Molecule Flow Stretching Assay Implementation for Studying Transport of Molecules Along DNA
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Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51
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科学领域:

  • 分子生物学
  • 合成生物学
  • 生物物理

背景情况:

  • 在DNA电路中,指掌介导的链位移 (TMSD) 是至关重要的.
  • 序列相似性可能导致交叉通话,导致电路故障.
  • 在复杂的环境中分析所有可能的相互作用是不可能的.

研究的目的:

  • 研究随机DNA序列对TMSD电路动力学的影响.
  • 在不同的序列背景下开发TMSD反应的预测模型.
  • 评估提高TMSD反应速度和强度的策略.

主要方法:

  • 研究个别干扰线程以收集动力数据.
  • 开发机器学习模型来估计TMSD反应动力学.
  • 研究了随机DNA序列池对TMSD反应的影响.
  • 对比了三种加速TMSD反应的技术.

主要成果:

  • 随机序列池中的动力学是由强烈相互作用的线程的小子集控制的.
  • 电路平衡与背景序列显著影响反应速度 (高达10倍的差异).
  • 所有测试的加速技术 (三字母字母,脚保护,阻塞链) 都是有效的.
  • 阻断字符串通过不施加序列约束提供了优势.

结论:

  • 对序列背景效应的洞察对于设计强大的TMSD电路至关重要.
  • 从有限的交互数据可以构建预测模型.
  • 阻断链在复杂环境中提供了增强TMSD反应的多功能方法.