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関連する概念動画

Lagging Strand Synthesis01:59

Lagging Strand Synthesis

54.0K
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...
54.0K
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

10.1K
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...
10.1K
The Replisome03:01

The Replisome

34.6K
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...
34.6K
Homologous Recombination02:31

Homologous Recombination

50.9K
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...
50.9K
DNA Replication02:40

DNA Replication

50.6K
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...
50.6K
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

5.9K
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,...
5.9K

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関連する実験動画

Updated: Sep 5, 2025

Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks
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Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks

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DNAストランドシプレッシブ タイムロジック回路

Anna P Lapteva1, Namita Sarraf1, Lulu Qian1,2

  • 1Bioengineering, California Institute of Technology, Pasadena, California 91125, United States.

Journal of the American Chemical Society
|July 5, 2022
PubMed
まとめ
この要約は機械生成です。

この研究では,信号のタイミングに基づいて意思決定を行うために タイムメモリとロジックゲートを使用する DNA 鎖移動回路を提示しています これらの回路は複雑な分子計算を可能にし, 知的人工分子機械の道を開きます.

さらに関連する動画

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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DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation
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DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation

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関連する実験動画

Last Updated: Sep 5, 2025

Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks
07:50

Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks

Published on: November 25, 2015

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

Published on: August 15, 2018

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DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation
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DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation

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科学分野:

  • 合成生物学
  • 分子コンピューティング
  • 生物化学

背景:

  • 時間的な情報処理は 分子的な意思決定に不可欠です
  • 相対的な信号のタイミングは 時間の情報の重要な側面です

研究 の 目的:

  • タイムロジック計算のための DNA 配列移位回路を実証する.
  • インプットの組み合わせと相対的なタイミングに基づいた意思決定を可能にします.

主な方法:

  • メモリストランドを使って 時間的な入力情報をエンコードする
  • 現在の信号と過去の信号を処理する 論理ゲートを設計する
  • 回路の最適化のために不一致とトホールドの短縮を活用する.

主要な成果:

  • タイムメモリとロジック機能を備えた DNA回路の構築に成功しました
  • マスマッチを使用した回路の複雑性の減少が実証されました.
  • 戦略的な足場変更によって回路の頑丈さを向上させました.
  • 実験指導のための詳細なモデリングの検証

結論:

  • DNA回路における時間記憶と論理計算の戦略を開発した.
  • デザインの原則は,複雑なタイムロジックと DNA ベースのニューラルネットワークに一般化できます.
  • 人工分子の機械に 知的行動の機会を 与えるのです