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Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
Exon Recombination02:32

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The evolution of new genes is critical for speciation. Exon recombination, also known as exon shuffling or domain shuffling, is an important means of new gene formation. It is observed across vertebrates, invertebrates, and in some plants such as potatoes and sunflowers. During exon recombination, exons from the same or different genes recombine and produce new exon-intron combinations, which might evolve into new genes. 
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Mismatch Repair01:20

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Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
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The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
Diversity of Antigen Receptors01:28

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Antigen receptors are essential components of the immune system crucial in defending the body against foreign invaders. These receptors are present on the surface of B and T cells, enabling them to recognize antigens and mount an appropriate immune response.
Before encountering any antigen, lymphocytes express these receptors. On B cells, the antigen receptor is a membrane-bound antibody molecule called BCR; on T cells, it is a T cell receptor or TCR. B and T cell receptors are composed of two...

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Video Experimental Relacionado

Updated: Jun 2, 2026

Assessing Somatic Hypermutation in Ramos B Cells after Overexpression or Knockdown of Specific Genes
08:12

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Published on: November 1, 2011

Daño colateral causado por la diversificación genética de los receptores de antígenos.

Grace K Mahowald1, Jason M Baron, Barry P Sleckman

  • 1Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.

Cell
|December 17, 2008
PubMed
Resumen
Este resumen es generado por máquina.

La desaminasa inducida por activación (AID) crea roturas de ADN en los oncogenes, lo que contribuye a los cánceres linfoides. AID y RAG pueden colaborar en estas rupturas, ofreciendo nuevos conocimientos sobre el desarrollo del cáncer.

Área de la Ciencia:

  • Biología molecular La biología molecular.
  • Genética del cáncer Genética del cáncer.
  • Inmunología Inmunología.

Sus antecedentes:

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  • Las translocaciones cromosómicas que unen genes de receptores de antígenos y oncogenes son comunes en las neoplasias linfoides malignas.
  • La desaminasa inducida por activación (AID) es crucial para la diversificación de los genes de los receptores de antígenos.