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Related Concept Videos

Homologous Recombination02:31

Homologous Recombination

The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

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...
RNA Editing02:23

RNA Editing

RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
Receptor Downregulation in MVBs01:15

Receptor Downregulation in MVBs

Multivesicular bodies (MVBs) are mature endosomes that sort ubiquitinated proteins and then fuse with lysosomes to degrade the sorted proteins. Epidermal growth factor (EGF) and its receptor (EGFR) form a complex that can be internalized through endocytosis, sorted into an MVB, and later degraded.
The EGFR can initiate signaling pathways that  lead to cell proliferation, migration, and differentiation. Overexpression of EGFR  stimulates cells to proliferate. Excessive  EGFR activation may...
Regulation of the Unfolded Protein Response01:31

Regulation of the Unfolded Protein Response

Inositol-requiring kinase one or IRE1 is the most conserved eukaryotic unfolded protein response (UPR) receptor. It is a type I transmembrane protein kinase receptor with a distinctive site-specific RNase activity. As the binding mechanics of the misfolded proteins with the N-terminal domain of IRE-1 are unclear, three binding models — direct, indirect, and allosteric -- are proposed for receptor activation. Nevertheless, it is known that once a misfolded protein associates with IRE1, it...
Diversity of Antigen Receptors01:28

Diversity of Antigen Receptors

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.
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Updated: May 11, 2026

RNA Catalyst as a Reporter for Screening Drugs against RNA Editing in Trypanosomes
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Published on: July 22, 2014

Immune receptor editing: revise and select

M C Nussenzweig1

  • 1Laboratory of Molecular Immunology, The Rockefeller University, Howard Hughes Medical Institute, New York, New York 10021, USA.

Cell
|January 6, 1999
PubMed
Summary

Secondary antigen receptor gene recombination, or receptor editing, salvages self-reactive lymphocytes before negative selection. This process, crucial in developing T and B cells, shapes immune responses and was not predicted by earlier theories.

Area of Science:

  • Immunology
  • Molecular Biology
  • Cell Biology

Background:

  • Secondary antigen receptor gene recombination occurs in both developing and mature lymphocytes.
  • Receptor editing in developing lymphocytes involves altering receptor specificity in response to autoantigens.
  • This process salvages self-reactive cells, preventing their elimination via negative selection.

Purpose of the Study:

  • To explore the phenomenon of receptor editing in lymphocytes.
  • To understand how antigen-induced receptor specificity changes can be integrated into existing immunological theories.
  • To highlight the importance of V(D)J recombination in mature lymphocytes.

Main Methods:

  • The study discusses the concept of receptor editing based on existing immunological principles and literature.

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Last Updated: May 11, 2026

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  • It references theoretical frameworks like the clonal selection theory and Jerne's suggestions.
  • The text implies a review and synthesis of knowledge regarding lymphocyte development and selection.
  • Main Results:

    • Receptor editing converts anti-self-reactive cells to non-self-reactive cells during lymphocyte development.
    • This mechanism salvages self-reactive clones before they undergo negative selection.
    • Antigen-induced changes in receptor specificity were not initially accounted for in clonal selection theory.

    Conclusions:

    • Receptor editing can be incorporated into the clonal selection theory by considering a specific developmental stage.
    • While less is known about V(D)J recombination in mature lymphocytes, it likely influences immune responses.
    • Antigen-induced receptor selection plays a significant role in shaping the overall immune response.