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Videos de Conceptos Relacionados

Methods of Nuclear Reprogramming01:24

Methods of Nuclear Reprogramming

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Nuclear reprogramming is a process of transforming one cell type into an unrelated cell type by epigenetic changes that alter the cell’s original gene expression pattern. Such epigenetic changes force cells to express a different set of genes, which play a significant role in inducing transformation into other cell types. Nuclear reprogramming offers applications in reproductive cloning for livestock propagation and regenerative medicine — developing patient-specific cells for...
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Somatic to iPS Cell Reprogramming01:29

Somatic to iPS Cell Reprogramming

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Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012...
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Chromatin Modification in iPS Cells01:32

Chromatin Modification in iPS Cells

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Chromatin modification alters gene expression; therefore, scientists can add histone-modifying enzymes, histone variants, and chromatin remodeling complexes to somatic cells to aid reprogramming into pluripotent stem (iPS) cells.
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
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Introduction to Nuclear Reprogramming01:14

Introduction to Nuclear Reprogramming

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Nuclear reprogramming is the process of switching gene expression of one cell type to that of another cell type, usually from a differentiated cell state to an undifferentiated cell state. Differentiation occurs during processes such as development and morphogenesis, tissue regeneration, and malignancy. Cells can also be artificially induced to reprogram their gene expression by techniques such as nuclear transfer, induced pluripotency, and cell fusion. Such techniques have many applications in...
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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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Epigenetic Regulation01:37

Epigenetic Regulation

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Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
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Video Experimental Relacionado

Updated: Jun 16, 2025

Application of RNAi and Heat-shock-induced Transcription Factor Expression to Reprogram Germ Cells to Neurons in C. elegans
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Application of RNAi and Heat-shock-induced Transcription Factor Expression to Reprogram Germ Cells to Neurons in C. elegans

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Reescribir el ADN regulador para diseccionar y reprogramar la expresión génica

Gabriella E Martyn1, Michael T Montgomery1, Hank Jones1

  • 1Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA; Basic Science and Engineering Initiative, Stanford Children's Health, Betty Irene Moore Children's Heart Center, Stanford, CA 94305, USA.

Cell
|April 17, 2025
PubMed
Resumen

Desarrollamos una nueva herramienta de detección CRISPR, Variant-EFFECTS, para editar con precisión el ADN regulador y medir los cambios en la expresión génica. Este método revela cómo las variaciones de la secuencia de ADN afectan la actividad génica y ofrece potencial para nuevas terapias de edición génica.

Palabras clave:
CRISPR y sus derivadosEl ARN FlowFISHMejoradoresregulación genéticacribado de alto rendimientoVariantes sin codificaciónModelos de predicciónEdición principaldiseño de la secuenciaFactores de transcripción

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Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers
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Last Updated: Jun 16, 2025

Application of RNAi and Heat-shock-induced Transcription Factor Expression to Reprogram Germ Cells to Neurons in C. elegans
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Application of RNAi and Heat-shock-induced Transcription Factor Expression to Reprogram Germ Cells to Neurons in C. elegans

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Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers
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Repressing Gene Transcription by Redirecting Cellular Machinery with Chemical Epigenetic Modifiers

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Área de la Ciencia:

  • La genómica
  • Biología molecular
  • Regulación genética

Sus antecedentes:

  • Las secuencias de ADN reguladoras controlan la expresión génica específica del tipo de célula a través de la unión al factor de transcripción.
  • La predicción del impacto funcional y la programabilidad del ADN regulador sigue siendo un desafío significativo en la biología molecular.

Objetivo del estudio:

  • Desarrollar un método de alto rendimiento para diseccionar la función de los elementos reguladores endógenos del ADN.
  • Reprogramar sistemáticamente los elementos reguladores y cuantificar los efectos de las ediciones diseñadas en la expresión génica.

Principales métodos:

  • Desarrollo y aplicación de efectos variantes (efectos variantes de los experimentos de clasificación de flujos con pantallas de orientación CRISPR).
  • Introducción de cientos de ediciones diseñadas para el ADN regulador endógeno en genes y tipos de células específicos.
  • Cuantificación de los cambios en la expresión génica utilizando la clasificación de flujo y las pantallas CRISPR.

Principales resultados:

  • La disección y reprogramación de tres elementos reguladores en dos genes y dos tipos de células.
  • Identificación de los efectos específicos del contexto genómico de los sitios de unión endógenos.
  • Actividades específicas del tipo de célula de los motivos de los factores de transcripción y limitaciones de los modelos de predicción computacional actuales.
  • Demostró que las pequeñas ediciones pueden ajustar la expresión génica en un amplio rango dinámico.

Conclusiones:

  • Variant-EFFECTS es una herramienta generalizable para diseccionar la función reguladora del ADN.
  • Estrategias de edición del genoma identificadas para ajustar con precisión la expresión génica en un contexto endógeno.
  • Los hallazgos sugieren el potencial de terapias basadas en la edición primaria dirigidas al ADN regulador para un control preciso de la expresión génica.