Jove
Visualize
Contáctanos

Videos de Conceptos Relacionados

Cooperative Binding of Transcription Regulators02:13

Cooperative Binding of Transcription Regulators

6.5K
Transcriptional regulators bind to specific cis-regulatory sequences in the DNA to regulate gene transcription. These cis-regulatory sequences are very short, usually less than ten nucleotide pairs in length. The short length means that there is a high probability of the exact same sequence randomly occurring throughout the genome.  Since regulators can also bind to groups of similar sequences, this further increases the chances of random binding. Transcriptional regulators form...
6.5K
Co-activators and Co-repressors02:04

Co-activators and Co-repressors

7.4K
Gene transcription is regulated by the synergistic action of several proteins that form a complex at a gene regulatory site. This is observed in eukaryotes, where the regulation of gene expression is a complex process. Regulatory proteins in eukaryotes can broadly be classified into two types – regulators that bind directly to specific DNA sequences and co-regulators that associate with regulatory proteins but cannot directly bind to the DNA. These co-regulators are further divided into...
7.4K
RNA Polymerase II Accessory Proteins02:36

RNA Polymerase II Accessory Proteins

9.3K
Proteins that regulate transcription can do so either via direct contact with RNA Polymerase or through indirect interactions facilitated by adaptors, mediators, histone-modifying proteins, and nucleosome remodelers. Direct interactions to activate transcription is seen in bacteria as well as in some eukaryotic genes. In these cases, upstream activation sequences are adjacent to the promoters, and the activator proteins interact directly with the transcriptional machinery. For example, in...
9.3K
Histone Modification02:32

Histone Modification

13.4K
The histone proteins have a flexible N-terminal tail extending out from the nucleosome. These histone tails are often subjected to post-translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination. Particular combinations of these modifications form “histone codes” that influence the chromatin folding and tissue-specific gene expression.
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone...
13.4K
Spreading of Chromatin Modifications02:25

Spreading of Chromatin Modifications

8.3K
The histone proteins in the nucleosomes are post-translationally modified (PTM) to increase or decrease access to DNA. The commonly observed PTMs are methylation, acetylation, phosphorylation, and ubiquitination of lysine amino acids in the histone H3 tail region. These histone modifications have specific meaning for the cell. Hence, they are called "histone code". The protein complex involved in histone modification is termed as "reader-writer" complex.
Writers
The writer...
8.3K
Transcription Factors02:16

Transcription Factors

76.2K
Tissue-specific transcription factors contribute to diverse cellular functions in mammals. For example, the gene for beta globin, a major component of hemoglobin, is present in all cells of the body. However, it is only expressed in red blood cells because the transcription factors that can bind to the promoter sequences of the beta globin gene are only expressed in these cells. Tissue-specific transcription factors also ensure that mutations in these factors may impair only the function of...
76.2K

También podría leer

Artículos Relacionados

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

Ordenar por
Same author

Recognition and silencing of a new transposable element.

Nature communications·2026
Same author

Structural analysis of OCT4 binding to human LIN28B nucleosomes.

Scientific reports·2026
Same author

Mechanisms of chromatin remodeling by the human Snf2-type ATPase SNF2H.

Cell research·2025
Same author

Mechanisms of chromatin remodeling by an Snf2-type ATPase.

bioRxiv : the preprint server for biology·2025
Same author

Illuminating nucleosome interactions.

Cell research·2024
Same author

ISWI catalyzes nucleosome sliding in condensed nucleosome arrays.

Nature structural & molecular biology·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: Jul 29, 2025

Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark
10:09

Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark

Published on: January 26, 2018

7.5K

Las modificaciones de la histona regulan la cooperatividad del factor de transcripción pionero

Kalyan K Sinha1, Silvija Bilokapic1, Yongming Du1

  • 1Department of Structural Biology, St. Jude Children's Research Hospital, Memphis, TN, USA.

Nature
|May 24, 2023
PubMed
Resumen

Los factores de transcripción pioneros como OCT4 y SOX2 cooperan para acceder al ADN compactado. Este estudio revela cómo la unión de OCT4 altera la estructura del nucleosoma, permitiendo la unión cooperativa y promoviendo la descomposición de la cromatina para la programación celular.

Más Videos Relacionados

Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers
10:28

Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers

Published on: September 20, 2018

6.5K
Author Spotlight: An Integrated Workflow to Study the Promoter-Centric Spatio-Temporal Genome Architecture in Scarce Cell Populations
11:36

Author Spotlight: An Integrated Workflow to Study the Promoter-Centric Spatio-Temporal Genome Architecture in Scarce Cell Populations

Published on: April 21, 2023

2.2K

Videos de Experimentos Relacionados

Last Updated: Jul 29, 2025

Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark
10:09

Isolation and Cultivation of Neural Progenitors Followed by Chromatin-Immunoprecipitation of Histone 3 Lysine 79 Dimethylation Mark

Published on: January 26, 2018

7.5K
Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers
10:28

Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers

Published on: September 20, 2018

6.5K
Author Spotlight: An Integrated Workflow to Study the Promoter-Centric Spatio-Temporal Genome Architecture in Scarce Cell Populations
11:36

Author Spotlight: An Integrated Workflow to Study the Promoter-Centric Spatio-Temporal Genome Architecture in Scarce Cell Populations

Published on: April 21, 2023

2.2K

Área de la Ciencia:

  • Biología molecular
  • La epigenética
  • Biología estructural

Sus antecedentes:

  • Los factores de transcripción pioneros (PTF) pueden acceder a la cromatina compactada.
  • La cooperación entre OCT4 y SOX2 es crucial para la pluripotencia y la reprogramación.
  • Los mecanismos de la función y la cooperación de PTF en la cromatina no se comprenden completamente.

Objetivo del estudio:

  • Aclarar los mecanismos moleculares de la función del factor de transcripción pionero OCT4 y la cooperación en la cromatina.
  • Determinar la base estructural para la remodelación de nucleosomas mediada por OCT4 y la unión al factor de transcripción.

Principales métodos:

  • Microscopía cryoelectrónica (cryo-EM) para determinar las estructuras de OCT4 unidas a los nucleosomas.
  • Ensayos bioquímicos para evaluar los cambios en la estructura de los nucleosomas y la unión al factor de transcripción.
  • Análisis de las interacciones de cola de histonas y modificaciones post-traducionales.

Principales resultados:

  • La unión de OCT4 induce cambios estructurales en los nucleosomas y reposiciona el ADN, facilitando la unión cooperativa de OCT4 y SOX2.
  • El dominio de activación de OCT4 interactúa con la cola N-terminal de la histona H4, promoviendo la descomposición de la cromatina.
  • El dominio de unión al ADN de OCT4 interactúa con la cola N-terminal de la histona H3, con modificaciones de H3K27 que afectan el posicionamiento del ADN y la cooperatividad del factor de transcripción.

Conclusiones:

  • OCT4 remodela activamente los nucleosomas para permitir su propia unión y la de SOX2, facilitando la cooperación del factor de transcripción.
  • Las interacciones entre OCT4 y las colas de histona (H3 y H4) son clave para la modulación de la cromatina.
  • El paisaje epigenético, a través de modificaciones histónicas como H3K27, puede regular la actividad OCT4 para una programación celular precisa.