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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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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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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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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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The DNA Replication Fork01:02

The DNA Replication Fork

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An organism’s genome needs to be duplicated in an efficient and error-free manner for its growth and survival. The replication fork is a Y-shaped active region where two strands of DNA are separated and replicated continuously. The coupling of DNA unzipping and complementary strand synthesis is a characteristic feature of a replication fork.   Organisms with small circular DNA, such as E. coli, often have a single origin of replication; therefore, they have only two replication...
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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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Video Experimental Relacionado

Updated: Jul 26, 2025

Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae
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Detection of Homologous Recombination Intermediates via Proximity Ligation and Quantitative PCR in Saccharomyces cerevisiae

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La replicación inducida por ruptura orquesta el cambio de plantilla dependiente de la resección

Tianpeng Zhang1, Yashpal Rawal2, Haoyang Jiang1

  • 1Department of Cancer Biology, Penn Center for Genome Integrity, Basser Center for BRCA, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Nature
|June 14, 2023
PubMed
Resumen
Este resumen es generado por máquina.

La síntesis de telómeros inducida por ruptura (BITS) utiliza un replicoma mínimo para la reparación del ADN. La nucleasa SNM1A dirige el PCNA ubiquitinado para promover la resección y el bypass de la lesión durante este proceso.

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Direct Restart of a Replication Fork Stalled by a Head-On RNA Polymerase
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Assessment of Global DNA Double-Strand End Resection using BrdU-DNA Labeling coupled with Cell Cycle Discrimination Imaging
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Área de la Ciencia:

  • Biología molecular
  • Reparación del ADN
  • Biología de los telómeros

Sus antecedentes:

  • La síntesis de telómeros inducida por ruptura (BITS) es una vía independiente de RAD51 crucial para el alargamiento alternativo de los telómeros.
  • BITS implica un replicoma mínimo, incluido el antígeno nuclear celular proliferante (PCNA) y la ADN polimerasa-δ, para una síntesis extensa de reparación de ADN.
  • La respuesta de BITS al estrés de replicación y a las estructuras secundarias de ADN no se comprende bien.

Objetivo del estudio:

  • Investigar la respuesta al daño del ADN durante el BITS bajo estrés de replicación.
  • Identificar las proteínas clave involucradas en el mantenimiento de la procesividad durante la reparación de recombinación homóloga de largo plazo.
  • Aclarar el mecanismo por el cual el BITS tolera estructuras complejas de ADN.

Principales métodos:

  • Inducción sincrónica de las rupturas de doble hilo.
  • Proteómica de segmentos de cromatina aislados (PICh) para analizar el proteoma de respuesta al daño del ADN telomérico.
  • Análisis de la ubiquitinación PCNA dependiente de RAD18 y de la actividad de la nucleasa SNM1A.

Principales resultados:

  • BITS provoca una respuesta al estrés de replicación caracterizada por la ubiquitinación PCNA dependiente de RAD18.
  • La nucleasa SNM1A se identifica como un efector clave de la tolerancia al daño del ADN ubiquitinado dependiente del PCNA.
  • SNM1A reconoce el PCNA ubiquitinado en el replicoma inducido por ruptura, dirigiendo su actividad de nucleasa para promover la resección.

Conclusiones:

  • La replicación inducida por ruptura orquesta el bypass de la lesión dependiente de la resección.
  • La actividad de la nucleasa SNM1A es crítica para la recombinación ubiquitinada dirigida por PCNA en células de mamíferos.
  • Este estudio revela un nuevo mecanismo para la tolerancia al daño del ADN durante el BITS.