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Lytic Cycle of Bacteriophages01:30

Lytic Cycle of Bacteriophages

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Bacteriophages, also known as phages, are specialized viruses that infect bacteria. A key characteristic of phages is their distinctive “head-tail” morphology. A phage begins the infection process (i.e., lytic cycle) by attaching to the outside of a bacterial cell. Attachment is accomplished via proteins in the phage tail that bind to specific receptor proteins on the outer surface of the bacterium. The tail injects the phage’s DNA genome into the bacterial cytoplasm. In the...
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Lysogenic Cycle of Bacteriophages00:43

Lysogenic Cycle of Bacteriophages

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In contrast to the lytic cycle, phages infecting bacteria via the lysogenic cycle do not immediately kill their host cell. Instead, they combine their genome with the host genome, allowing the bacteria to replicate the phage DNA along with the bacterial genome. The incorporated copy of the phage genome is called the prophage. Some prophages can re-activate and enter the lytic cycle. This often occurs in response to a perturbation, such as DNA damage, but can also transpire in the absence of...
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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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Retroviruses02:33

Retroviruses

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Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
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CRISPR and crRNAs02:53

CRISPR and crRNAs

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Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
The CRISPR-Cas system stores a copy of foreign DNA in the host genome and uses it to identify the foreign DNA upon reinfection. CRISPR-Cas has three different...
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Intracellular Movement of Viruses and Bacteria01:10

Intracellular Movement of Viruses and Bacteria

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Intracellular bacteria and viruses often comprise a group of highly infectious pathogens that can cause several diseases. Bacterial pathogens include those belonging to the genus Rickettsia responsible for conditions such as rocky mountain spotted fever and the Mediterranean spotted fever; Chlamydia, a genus responsible for a sexually transmitted disease; Coxiella burnetii, an agent responsible for Q fever. Viral pathogens include vaccinia—a poxvirus, and herpes simplex virus—a...
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Video Experimental Relacionado

Updated: Jun 14, 2025

Phage-Mediated Genetic Manipulation of the Lyme Disease Spirochete Borrelia burgdorferi
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Phage-Mediated Genetic Manipulation of the Lyme Disease Spirochete Borrelia burgdorferi

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Engañar a los fagos con un movimiento inverso

Ilya Osterman1, Rotem Sorek1

  • 1Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.

Science (New York, N.Y.)
|August 29, 2024
PubMed
Resumen
Este resumen es generado por máquina.

Un nuevo gen antiviral, aunque no está presente en el ADN, se expresa activamente. Esta expresión ocurre a través de un proceso único llamado transcripción inversa de círculo rodante, que ofrece nuevos conocimientos sobre los mecanismos antivirales.

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Área de la Ciencia:

  • Biología molecular
  • Virología
  • La genética

Sus antecedentes:

  • El dogma central de la biología molecular típicamente describe el ADN como la plantilla para la síntesis de ARN y proteínas.
  • La expresión génica generalmente se basa en la presencia de una secuencia de ADN que codifica el gen.
  • Los mecanismos de expresión génica no convencionales desafían la comprensión biológica tradicional.

Objetivo del estudio:

  • Para investigar la expresión de un gen antiviral que carece de una contraparte de ADN.
  • Para aclarar el mecanismo de la expresión génica en ausencia de una plantilla de ADN.
  • Para entender el papel de la transcripción inversa del círculo rodante en la defensa antiviral.

Principales métodos:

  • Análisis de genomas virales y elementos de ADN extracromosómico.
  • Detección y caracterización de las transcripciones de ARN.
  • Validación experimental de la actividad de transcripción inversa del círculo rodante.
  • Pruebas antivirales para evaluar la función genética.

Principales resultados:

  • Se identificó un gen antiviral y se confirmó su expresión.
  • No se encontró ninguna secuencia de ADN correspondiente para este gen antiviral en el huésped o en el genoma viral.
  • Se demostró que la transcripción inversa del círculo rodante es el mecanismo para expresar el gen antiviral.
  • El gen antiviral expresado exhibió una actividad antiviral significativa contra patógenos específicos.

Conclusiones:

  • La expresión génica puede ocurrir independientemente de una plantilla de ADN a través de mecanismos alternativos.
  • La transcripción inversa del círculo rodante representa una nueva vía para generar moléculas antivirales funcionales.
  • Este descubrimiento amplía nuestra comprensión del flujo de información genética y las estrategias antivirales.