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Videos de Conceptos Relacionados

Covalently Linked Protein Regulators02:04

Covalently Linked Protein Regulators

Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein.
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

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, a...
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

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...
Riboswitches01:56

Riboswitches

Riboswitches are non-coding mRNA domains that regulate the transcription and translation of downstream genes without the help of proteins. Riboswitches bind directly to a metabolite and can form unique stem-loop or hairpin structures in response to the amount of the metabolite present. They have two distinct regions – a metabolite-binding aptamer and an expression platform.
The aptamer has high specificity for a particular metabolite which allows riboswitches to specifically regulate...
Covalently Linked Protein Regulators02:04

Covalently Linked Protein Regulators

Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein.
Transcriptional Regulation: Riboswitches01:23

Transcriptional Regulation: Riboswitches

Riboswitches are RNA elements that regulate gene expression by altering their secondary structures in response to specific effector molecules. These elements, located in the leader regions of certain mRNAs, act as transcriptional regulators by toggling between alternative conformations to control downstream gene expression. Riboswitch-mediated regulation is a precise mechanism for modulating biosynthetic pathways, as exemplified by the riboflavin biosynthesis pathway in Bacillus...

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Video Experimental Relacionado

Updated: Jun 25, 2026

In Vivo Detection and Analysis of Rb Protein SUMOylation in Human Cells
09:40

In Vivo Detection and Analysis of Rb Protein SUMOylation in Human Cells

Published on: November 2, 2017

La SUMOilación regula el conmutador de plantilla mediado por Rad18

Dana Branzei1, Fabio Vanoli, Marco Foiani

  • 1IFOM, the FIRC Institute for Molecular Oncology Foundation, IFOM-IEO Campus, Via Adamello 16, 20139 Milan, Italy. dana.branzei@ifom-ieo-campus.it

Nature
|December 19, 2008
PubMed
Resumen
Este resumen es generado por máquina.

Este estudio revela que la proteína Rad18 es crucial para el desvío del daño del ADN en las horquillas de replicación de la levadura, coordinando el cambio de plantilla y la recombinación a través de las vías de ubicuidad de PCNA y SUMOilación.

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In Vitro SUMOylation Assay to Study SUMO E3 Ligase Activity
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In Vitro SUMOylation Assay to Study SUMO E3 Ligase Activity

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Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51
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Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51

Published on: February 13, 2019

Videos de Experimentos Relacionados

Last Updated: Jun 25, 2026

In Vivo Detection and Analysis of Rb Protein SUMOylation in Human Cells
09:40

In Vivo Detection and Analysis of Rb Protein SUMOylation in Human Cells

Published on: November 2, 2017

In Vitro SUMOylation Assay to Study SUMO E3 Ligase Activity
09:45

In Vitro SUMOylation Assay to Study SUMO E3 Ligase Activity

Published on: January 29, 2018

Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51
06:24

Real-time Observation of the DNA Strand Exchange Reaction Mediated by Rad51

Published on: February 13, 2019

Área de la Ciencia:

  • Biología Molecular Biología Molecular
  • Genética La genética.
  • La bioquímica es la bioquímica.

Sus antecedentes:

  • La conmutación de plantillas es un mecanismo clave para el desvío de daños en el ADN y el llenado de huecos durante la replicación.
  • La reparación de llenado de vacíos implica la recombinación homóloga y la poliubiquitilación del antígeno nuclear celular proliferante (PCNA) mediado por Rad18 y Rad5.
  • La coordinación entre estas vías de reparación y la evidencia física para el cambio de plantilla en las horquillas de replicación sigue sin estar clara.

Objetivo del estudio:

  • Para investigar la coordinación entre el bypass del daño del ADN, la recombinación homóloga y la ubicuidad del PCNA.
  • Para proporcionar evidencia física de la conmutación de la plantilla Rad18-Rad5-dependiente en las horquillas de replicación.
  • Para aclarar los roles de la ubicuidad de PCNA y la SUMOilación en la recombinación acoplada a la replicación.

Principales métodos:

  • Enfoques genéticos en el Saccharomyces cerevisiae.
  • Detección física de las uniones de cromatidas hermanas en forma de X (SCJ).
  • Análisis de las vías de poliubiquitilación y SUMOilación de PCNA.

Principales resultados:

  • Rad18 es esencial para la formación de SCJs en las horquillas de replicación dañadas, lo que implica la poliubiquitilación de PCNA a través de Mms2 y Ubc13.
  • El desvío del daño a través de SCJs requiere Ubc9, SUMOylated PCNA, y está coordinado con la recombinación Rad51-dependiente.
  • El estudio propone que las SCJs Rad18-Rad5-Mms2-dependientes representen eventos de cambio de plantilla.

Conclusiones:

  • Las vías de ubicuidad de PCNA y SUMOylación son críticas para promover eventos de recombinación transitorios, inducidos por daño y acoplados a la replicación.
  • Las uniones de cromatidas hermanas en las bifurcaciones de replicación juegan un papel en estos eventos de recombinación.
  • Este trabajo desenmascara un mecanismo coordinado para la tolerancia al daño del ADN que implica el cambio de plantilla y la recombinación.