V(D)J recombination - ορισμός. Τι είναι το V(D)J recombination
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Τι (ποιος) είναι V(D)J recombination - ορισμός

THE PROCESS IN WHICH IMMUNE RECEPTOR V, D, AND J, OR V AND J GENE SEGMENTS, DEPENDING ON THE SPECIFIC RECEPTOR, ARE RECOMBINED WITHIN A SINGLE LOCUS UTILIZING THE CONSERVED HEPTAMER AND NONOMER RECOMBINATION SIGNAL SEQUENCES (RSS).
VDJ recombination; Antibody gene rearrangement; VDJ recombinase; V(D)J recombinase; Antibody gene recombination; Gene arrangement; Gene re-arrangement; V-J joining; VJ recombinase; Combinatorial diversification; 12/23 rule; Somatic recombination model; Gene rearrangement; Immunogobulin gene; J gene segment; D gene segment; D segment; J segment; J region; Joining gene segment; Diversity gene segment; Vdj recombinase
  • Simplistic overview of V(D)J recombination of immunoglobulin heavy chains

V(D)J recombination         
V(D)J recombination is the mechanism of somatic recombination that occurs only in developing lymphocytes during the early stages of T and B cell maturation. It results in the highly diverse repertoire of antibodies/immunoglobulins and T cell receptors (TCRs) found in B cells and T cells, respectively.
Homologous recombination         
  • phases of the cell cycle]].
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  • homozygous]] for the agouti gene.
  • '''Figure 4.''' Double-strand break repair models that act via homologous recombination
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  • three main groups]] of life: archaea, bacteria and eukaryotes.
  •  '''Figure 5.''' The DSBR and SDSA pathways follow the same initial steps, but diverge thereafter. The DSBR pathway most often results in chromosomal crossover (bottom left), while SDSA always ends with non-crossover products (bottom right).
  • 3']] overhang is visible to the right of center.
  • '''Figure 9.''' Joining of single-ended double strand breaks could lead to rearrangements
  •  '''Figure 2.''' An early illustration of crossing over from [[Thomas Hunt Morgan]]
  • Schematic representation of the s2m RNA secondary structure, with tertiary structural interactions indicated as long range contacts.
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DNA RECOMBINATION PROCESS
Homolog recombination; Legitimate recombination; Recombinational repair; General recombination; Recombination repair; Homologous recombinational; Homologous recombination deficiency; Strand Invasion; Homologous recombination repair
Homologous recombination is a type of genetic recombination in which genetic information is exchanged between two similar or identical molecules of double-stranded or single-stranded nucleic acids (usually DNA as in cellular organisms but may be also RNA in viruses). It is widely used by cells to accurately repair harmful breaks that occur on both strands of DNA, known as double-strand breaks (DSB), in a process called homologous recombinational repair (HRR).
Recombination-activating gene         
AN INSTANCE OF MACROMOLECULAR COMPLEX IN HOMO SAPIENS WITH REACTOME ID (R-HSA-8865713)
RAG-1; RAG-2; Recombination activity gene; Rag proteins; Rag protein; RAG protein; Recombination activating gene
The recombination-activating genes (RAGs) encode parts of a protein complex that plays important roles in the rearrangement and recombination of the genes encoding immunoglobulin and T cell receptor molecules. There are two recombination-activating genes RAG1 and RAG2, whose cellular expression is restricted to lymphocytes during their developmental stages.

Βικιπαίδεια

V(D)J recombination

V(D)J recombination is the mechanism of somatic recombination that occurs only in developing lymphocytes during the early stages of T and B cell maturation. It results in the highly diverse repertoire of antibodies/immunoglobulins and T cell receptors (TCRs) found in B cells and T cells, respectively. The process is a defining feature of the adaptive immune system.

V(D)J recombination in mammals occurs in the primary lymphoid organs (bone marrow for B cells and thymus for T cells) and in a nearly random fashion rearranges variable (V), joining (J), and in some cases, diversity (D) gene segments. The process ultimately results in novel amino acid sequences in the antigen-binding regions of immunoglobulins and TCRs that allow for the recognition of antigens from nearly all pathogens including bacteria, viruses, parasites, and worms as well as "altered self cells" as seen in cancer. The recognition can also be allergic in nature (e.g. to pollen or other allergens) or may match host tissues and lead to autoimmunity.

In 1987, Susumu Tonegawa was awarded the Nobel Prize in Physiology or Medicine "for his discovery of the genetic principle for generation of antibody diversity".