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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.
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LTR retrotransposons are class I transposable elements with long terminal repeats flanking an internal coding region. These elements are less abundant in mammals compared to other class I transposable elements. About 8 percent of human genomic DNA comprises LTR retrotransposons. Some of the common examples of LTR retrotransposons are Ty elements in yeast and Copia elements in Drosophila.
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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...
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Master transcription regulators are regulatory proteins that are predominantly responsible for regulating the expression of multiple genes. Often these genes work in concert to drive a  complex process. Activation of a master transcription regulator can lead to a cascade of transcriptional activation necessary for that outcome. These regulators can directly bind to the regulatory sequences of the various genes involved, or they can indirectly regulate transcription by binding to regulatory...
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Updated: Nov 30, 2025

In vivo Application of the REMOTE-control System for the Manipulation of Endogenous Gene Expression
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Los programas de transcripción persistentes están asociados con la memoria remota

Michelle B Chen1, Xian Jiang2,3, Stephen R Quake4,5

  • 1Department of Bioengineering, Stanford University, Stanford, CA, USA.

Nature
|November 12, 2020
PubMed
Resumen
Este resumen es generado por máquina.

Los recuerdos remotos que duran toda la vida implican cambios persistentes en la expresión génica de las neuronas de la corteza prefrontal medial. Los astrocitos y la microglía también muestran cambios en la expresión génica, lo que indica su papel activo en el almacenamiento de la memoria.

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Área de la Ciencia:

  • La neurociencia
  • Biología molecular
  • La genética

Sus antecedentes:

  • El papel de la expresión génica en la memoria a corto plazo está bien estudiado.
  • Los mecanismos de almacenamiento remoto a largo plazo y de por vida siguen siendo en gran medida desconocidos.
  • La corteza prefrontal medial está implicada en la consolidación y recuperación de la memoria.

Objetivo del estudio:

  • Para investigar el paisaje de expresión génica de una sola célula de almacenamiento remoto de memoria.
  • Identificar los mecanismos moleculares que subyacen al mantenimiento de la memoria a largo plazo.
  • Para explorar la contribución de las células gliales a la memoria remota.

Principales métodos:

  • Utilizó un paradigma de memoria de miedo contextual a largo plazo en ratones.
  • Se realizó la secuenciación de ARN de una sola célula para analizar la expresión génica.
  • El análisis se centró en la corteza prefrontal medial.

Principales resultados:

  • Se identificaron alteraciones transcripcionales persistentes y específicas de la actividad en las neuronas semanas después del aprendizaje.
  • Descubrieron genes relacionados con la fusión de la membrana potencialmente involucrados en el mantenimiento de la memoria.
  • Se observaron firmas persistentes de expresión génica en los astrocitos y la microglía asociadas con la memoria.

Conclusiones:

  • El almacenamiento remoto de memoria implica programas de expresión génica sostenidos y específicos del tipo de célula.
  • Las células gliales, incluidos los astrocitos y la microglia, participan activamente en los circuitos de memoria remota.
  • Los hallazgos contribuyen a comprender los estados celulares dependientes de la actividad y los mecanismos de memoria.