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相关概念视频

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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Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

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Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
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Next-generation Sequencing

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The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
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Restarting Stalled Replication Forks02:37

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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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Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks
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尼克辅助反应物回收以实现驱动的DNA电路

Cheng Zhang1,2, Zhiyu Wang3, Yan Liu

  • 1School of Electronics Engineering and Computer Science , Peking University , Beijing 100871 , China.

Journal of the American Chemical Society
|September 21, 2019
PubMed
概括

合成DNA电路可以在分子编程中进行信号放大. 一个新的nicking辅助回收策略提高了反应物在驱动的DNA电路中的可回收性,提高了合成生物学应用的效率.

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科学领域:

  • 合成生物学
  • 分子编程
  • 生物化学

背景情况:

  • 催化DNA电路对于分子编程中的信号放大至关重要.
  • 反应剂的回收对于这些电路的连续运行至关重要.
  • 提高因驱动的DNA回路的可回收性是一个关键挑战.

研究的目的:

  • 在驱动的DNA回路中开发和实施一种新的助回收策略.
  • 提高分子编程的DNA电路的效率和可回收性.
  • 在单层和双层电路设计中研究该策略的性能.

主要方法:

  • 实施一项除辅助回收策略,将DNA废物转化为活性成分.
  • 构建和分析单层和多层双层驱动的DNA电路.
  • 在燃料DNA消化和触发释放过程中评估反应物的循环.

主要成果:

  • 单层催化电路有效消耗多余的燃料DNA而不会耗尽门组件.
  • 在燃料DNA消化过程中观察到双层回路的回收,但在下游触发释放过程中没有.
  • 证明了双重DNA废物产品在随后的反应周期中重新转化为活性成分的能力.

结论:

  • 助回收策略提供了一种简单而通用的方法来改进由驱动的DNA电路.
  • 这种方法提高了DNA电路的效率,用于分子编程和合成生物学.
  • 该战略有助于创建更强大,更可持续的催化DNA系统.