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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

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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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Homologous Recombination02:31

Homologous Recombination

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Gene Conversion02:08

Gene Conversion

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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

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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...
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Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

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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...
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Video Experimental Relacionado

Updated: Apr 21, 2026

Analyzing and Building Nucleic Acid Structures with 3DNA
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Interconversión entre tres estructuras de ADN sobreestiradas.

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
Resumen
Este resumen es generado por máquina.

Los investigadores estudiaron las transiciones de sobreestiramiento del ADN inducidas por cambios en la concentración de sal. Observaron interconversiones directas entre la burbuja de ADN, el ADN-S y las estructuras de ADN de una sola hebra peladas (ADNss) bajo fuerza, con la conversión de ADN ss pelado a ADN-S que muestra una cinética lenta.

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Área de la Ciencia:

  • La biofísica es la biofísica.
  • Biología Molecular Biología Molecular
  • Biología Estructural Biología estructural.

Sus antecedentes:

  • El ADN de doble cadena (dsDNA) exhibe complejas transiciones estructurales bajo estrés mecánico.
  • El ADN no restringido por torsión puede adoptar conformaciones sobreestiradas como el ADN de una sola hebra pelado (ssDNA), la burbuja de ADN y el ADN-S a altas fuerzas.

Objetivo del estudio:

  • Para investigar la dinámica de interconversión entre diferentes estructuras de ADN sobreestiradas.
  • Para entender la influencia de la concentración de sal en estas transiciones estructurales a fuerza constante.

Principales métodos:

  • Utilizó la microscopía de fuerza atómica o técnicas similares de espectroscopia de fuerza de una sola molécula.
  • Se aplicaron fuerzas controladas (por encima de 70 pN) y concentraciones variadas de NaCl.
  • Cambios de extensión gradual observados indicativos de interconversiones estructurales.

Principales resultados:

  • Se han demostrado interconversiones directas entre el ADN-S y las estructuras de burbujas de ADN en construcciones de ADN cerradas.
  • Mostró interconversiones directas entre el ADN-S y el ADN-ss pelado en construcciones de ADN con extremo abierto.
  • Se identificó una cinética ultra lenta para la conversión de ssDNA pelado a S-ADN, atribuida a la formación secundaria de horquilla.

Conclusiones:

  • La concentración de sal juega un papel crucial en la mediación de las interconversiones entre las estructuras de ADN sobreestiradas.
  • La cinética observada proporciona información sobre los mecanismos moleculares que gobiernan la plasticidad estructural del ADN bajo la fuerza.
  • Los hallazgos mejoran la comprensión del comportamiento del ADN en condiciones no fisiológicas y su versatilidad estructural.