Jove
Visualize
Contáctanos

Videos de Conceptos Relacionados

Positive Regulator Molecules01:45

Positive Regulator Molecules

To consistently produce healthy cells, the cell cycle—the process that generates daughter cells—must be precisely regulated.
Positive Regulator Molecules02:39

Positive Regulator Molecules

Mitotic cell division results in daughter cells that exactly resemble the parent cell. However, errors in the DNA replication or distribution of genetic material may lead to genetic mutations that may be passed down to every new cell formed from the resulting abnormal cell. Propagation of such mutant cells is restricted through checkpoint mechanisms present at different stages of the cell cycle. These checkpoints involve regulator molecules that either promote or demote cell cycle events.
Inhibition of Cdk Activity02:34

Inhibition of Cdk Activity

The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
S-Cdk Initiates DNA Replication02:38

S-Cdk Initiates DNA Replication

The cell cycle is a series of events leading to DNA duplication followed by the division of cell content to form two daughter cells. The cell cycle progresses in four stages—the cell increases in size (gap 1 or G1-phase), duplicates its DNA (synthesis or S-phase), prepares to divide (gap 2 or G2-phase), and divides (mitosis or M-phase).
Two states at the origin of replication
In eukaryotes, the initiation of replication occurs at many sites on the chromosomes, called the origins of replication.
Inhibition of CDK Activity02:34

Inhibition of CDK Activity

The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
S-Cdk Initiates DNA Replication02:38

S-Cdk Initiates DNA Replication

The cell cycle is a series of events leading to DNA duplication followed by the division of cell content to form two daughter cells. The cell cycle progresses in four stages—the cell increases in size (gap 1 or G1-phase), duplicates its DNA (synthesis or S-phase), prepares to divide (gap 2 or G2-phase), and divides (mitosis or M-phase).
Two states at the origin of replication
In eukaryotes, the initiation of replication occurs at many sites on the chromosomes, called the origins of replication.

También podría leer

Artículos Relacionados

Artículos vinculados a este trabajo por autores compartidos, revista y gráfico de citas.

Ordenar por
Same author

Correction to: Assessing SMC Complex Function in Replication Fork Progression with DNA Fiber Assays.

Methods in molecular biology (Clifton, N.J.)·2026
Same author

Assessing SMC Complex Function in Replication Fork Progression with DNA Fiber Assays.

Methods in molecular biology (Clifton, N.J.)·2025
Same author

Spontaneous Splenic Rupture as an Uncommon Complication of Acute Pancreatitis.

European journal of case reports in internal medicine·2025
Same author

Randomized Controlled Trial Demonstrates Efficacy of a Culturally Adapted Behavioral Intervention Delivered in Spanish by Community Health Workers to Reduce Unhealthy Alcohol Use Among Latino/as.

Journal of studies on alcohol and drugs·2025
Same author

DNA polymerase α/primase extraction from chromatin by VCP/p97 restricts ATR activation during unperturbed DNA replication.

Nature communications·2025
Same author

Interference of small compounds and Mg<sup>2+</sup> with dsRNA-binding fluorophores compromises the identification of SARS-CoV-2 RdRp inhibitors.

Scientific reports·2024
JoVE
x logofacebook logolinkedin logoyoutube logo
ACERCA DE JoVE
Visión GeneralLiderazgoBlogCentro de Ayuda JoVE
AUTORES
Proceso de PublicaciónConsejo EditorialAlcance y PolíticasRevisión por ParesPreguntas FrecuentesEnviar
BIBLIOTECARIOS
TestimoniosSuscripcionesAccesoRecursosConsejo Asesor de BibliotecasPreguntas Frecuentes
INVESTIGACIÓN
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchivo
EDUCACIÓN
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualCentro de Recursos para ProfesoresSitio de Profesores
Términos y Condiciones de Uso
Política de Privacidad
Políticas

Video Experimental Relacionado

Updated: Jun 21, 2026

Studying Cell Cycle-regulated Gene Expression by Two Complementary Cell Synchronization Protocols
12:02

Studying Cell Cycle-regulated Gene Expression by Two Complementary Cell Synchronization Protocols

Published on: June 6, 2017

La proliferación celular sin la ciclina E-CDK2

Juan Méndez1

  • 1Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.

Cell
|August 28, 2003
PubMed
Resumen

Los ratones pueden desarrollarse sin las ciclinas E1 y E2, pero estas proteínas son cruciales para la progresión del ciclo celular. Específicamente, las ciclinas E1 y E2 son esenciales para la endoreplicación y la quiescencia de salida en las células del ratón.

Área de la Ciencia:

  • Biología celular Biología celular.
  • Biología del desarrollo Biología del desarrollo.
  • Genética molecular genética molecular.

Sus antecedentes:

  • Las ciclinas son reguladores clave del ciclo celular.
  • Se sabe que las proteínas ciclina E (E1 y E2) juegan un papel en la proliferación celular.
  • La necesidad específica de las ciclinas E1 y E2 en el desarrollo embrionario de mamíferos y la salida del ciclo celular no se ha aclarado completamente.

Objetivo del estudio:

  • Investigar el papel de las ciclinas E1 y E2 en el desarrollo embrionario del ratón.
  • Para determinar la función de las ciclinas E1 y E2 en la proliferación de los fibroblastos.
  • Evaluar el requisito de las ciclinas E1 y E2 para la endoreplicación y la salida de la quiescencia.

Principales métodos:

  • Generación de ratones que carecen tanto de los genes de la ciclina E1 como de la ciclina E2 (doble nocaut).

Más Videos Relacionados

Combining Mitotic Cell Synchronization and High Resolution Confocal Microscopy to Study the Role of Multifunctional Cell Cycle Proteins During Mitosis
08:33

Combining Mitotic Cell Synchronization and High Resolution Confocal Microscopy to Study the Role of Multifunctional Cell Cycle Proteins During Mitosis

Published on: December 5, 2017

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay
12:26

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay

Published on: May 3, 2018

Videos de Experimentos Relacionados

Last Updated: Jun 21, 2026

Studying Cell Cycle-regulated Gene Expression by Two Complementary Cell Synchronization Protocols
12:02

Studying Cell Cycle-regulated Gene Expression by Two Complementary Cell Synchronization Protocols

Published on: June 6, 2017

Combining Mitotic Cell Synchronization and High Resolution Confocal Microscopy to Study the Role of Multifunctional Cell Cycle Proteins During Mitosis
08:33

Combining Mitotic Cell Synchronization and High Resolution Confocal Microscopy to Study the Role of Multifunctional Cell Cycle Proteins During Mitosis

Published on: December 5, 2017

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay
12:26

Identification of Cyclin-dependent Kinase 1 Specific Phosphorylation Sites by an In Vitro Kinase Assay

Published on: May 3, 2018

  • Cultivo y análisis de fibroblastos derivados de embriones de doble knockout.
  • Evaluación de la proliferación celular, la endoreplicación y la salida de la quiescencia en células de tipo salvaje y knockout.
  • Principales resultados:

    • Los ratones que carecen de ciclinas E1 y E2 pueden completar el desarrollo embrionario.
    • Los fibroblastos de los embriones de doble knockout muestran una proliferación normal in vitro.
    • Las ciclinas E1 y E2 son indispensables para la endoreplicación y la transición de la quiescencia al ciclo celular activo.

    Conclusiones:

    • Las ciclinas E1 y E2 no son esenciales para el desarrollo embrionario o la proliferación de fibroblastos básicos.
    • Estas ciclinas específicas juegan un papel crítico en los procesos especializados del ciclo celular, a saber, la endoreplicación y la salida de la quiescencia.