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DNA Topoisomerases02:02

DNA Topoisomerases

31.7K
Topoisomerases are enzymes that relax overwound DNA molecules during various cell processes, including DNA replication and transcription. These enzymes regulate positive and negative DNA supercoiling without changing the nucleotide sequence. DNA overwinding in a clockwise direction results in positively supercoiled DNA, whereas underwinding in a counterclockwise direction produces negatively supercoiled DNA.
Types and Mechanism of action
Topoisomerases are divided into two main types. ...
31.7K
Homologous Recombination02:31

Homologous Recombination

58.5K
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...
58.5K
Homologous Recombination02:31

Homologous Recombination

6.1K
6.1K
Gene Conversion02:08

Gene Conversion

9.2K
Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
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DNA Helicases00:55

DNA Helicases

19.1K
DNA unwinding helicase enzymes are a type of motor protein. Motor proteins can translocate along filaments or polymers using energy generated from ATP hydrolysis. Helicases are involved in all the important cellular processes where DNA unwinding is required, such as DNA replication, repair, recombination, and transcription. They are present in all living organisms, but vary in their structure, function, and mechanism of action. For example, in prokaryotes, DnaB helicase binds and translocates...
19.1K
Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

12.0K
The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
12.0K

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Updated: Apr 21, 2026

Analyzing and Building Nucleic Acid Structures with 3DNA
16:24

Analyzing and Building Nucleic Acid Structures with 3DNA

Published on: April 26, 2013

20.3K

3つの過剰に伸びたDNA構造の間の相互変換

Xinghua Zhang1, Yuanyuan Qu, Hu Chen

  • 1BioSystems and Micromechanics, Singapore-MIT Alliance for Research and Technology , Singapore 138602, Singapore.

Journal of the American Chemical Society
|October 23, 2014
PubMed
まとめ
この要約は機械生成です。

研究者は,塩分濃度の変化によって誘発されるDNAの過伸縮の移行を研究した. 彼らは,DNAバブル,S-DNA,および剥離された単一鎖DNA (ssDNA) 構造の間の直接的な相互変換を力の下で観察し,剥離されたssDNAからS-DNAへの変換が遅い運動を示しました.

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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

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Stretching Short Sequences of DNA with Constant Force Axial Optical Tweezers
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Stretching Short Sequences of DNA with Constant Force Axial Optical Tweezers

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関連する実験動画

Last Updated: Apr 21, 2026

Analyzing and Building Nucleic Acid Structures with 3DNA
16:24

Analyzing and Building Nucleic Acid Structures with 3DNA

Published on: April 26, 2013

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Design and Synthesis of a Reconfigurable DNA Accordion Rack
07:44

Design and Synthesis of a Reconfigurable DNA Accordion Rack

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Stretching Short Sequences of DNA with Constant Force Axial Optical Tweezers
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Stretching Short Sequences of DNA with Constant Force Axial Optical Tweezers

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科学分野:

  • バイオフィジックス 生物物理学
  • 分子生物学は分子生物学である.
  • 構造生物学 構造生物学とは

背景:

  • 二重鎖DNA (dsDNA) は,機械的ストレス下での複雑な構造的移行を示しています.
  • トルション制限のないDNAは,剥がれた単一鎖DNA (ssDNA),DNAバブル,および高い力でのS-DNAのような過度に伸びた形状を採用することができます.

研究 の 目的:

  • 異なる超伸縮DNA構造間の相互変換ダイナミクスを調査する.
  • 恒定力でのこれらの構造的移行に対する塩濃度の影響を理解するために.

主な方法:

  • 原子力顕微鏡や類似の単分子力スペクトロスコピーの技術を使用した.
  • 適用された制御力 (70pN以上) と,さまざまなNaCl濃度.
  • 構造的な相互変換を示す段階的な拡張変化が観察されました.

主要な成果:

  • エンドクローズドDNA構造におけるS-DNAとDNAバブル構造の間の直接的な相互変換が実証された.
  • エンドオープンのDNA構造でS-DNAと剥がれたssDNAの間の直接的な相互変換を展示しました.
  • 二次性ヘアピン形成に起因する,剥がれたssDNAをS-DNAに変換するための超低速の動力学が特定されました.

結論:

  • 塩の濃度は,過剰に張られたDNA構造間の相互変換を媒介する上で重要な役割を果たします.
  • 観察された運動学は,力によるDNA構造の可塑性を支配する分子機構の洞察を提供します.
  • 発見は,非生理学的条件におけるDNAの行動とその構造的多用途性の理解を高める.