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  2. V (D)J recombination - Wikipedia

    en.wikipedia.org/wiki/V(D)J_recombination

    All other gene segments between V and D segments are now deleted from the cell's genome. Primary transcript (unspliced RNA) is generated containing the VDJ region of the heavy chain and both the constant mu and delta chains (C μ and C δ). (i.e. the primary transcript contains the segments: V-D-J-C μ-C δ). The primary RNA is processed to add ...

  3. Organization and expression of immunoglobulin genes

    en.wikipedia.org/wiki/Organization_and...

    The rearrangements of heavy-chains are different from the light chains because DNA undergoes rearrangements of V-D-J gene segments in the heavy chains. These reorganizations of gene segments produce gene sequence from 5 prime to 3 prime ends such as a short leader exon, an intron, a joined VDJ segment, a second intron and several gene segments.

  4. Recombination signal sequences - Wikipedia

    en.wikipedia.org/wiki/Recombination_Signal_Sequences

    [1] [4] The RAG1/RAG2 complex then introduces a nick at the 5' end of the RSS heptamers adjacent to the coding regions on both the D and J segments, permanently removing the loop of intervening DNA and creating a double-stranded break that is repaired by VDJ recombinase enzymes. [1] [4] This process is repeated for the joining of V to DJ. [1]

  5. Gene structure - Wikipedia

    en.wikipedia.org/wiki/Gene_structure

    Gene structure is the organisation of specialised sequence elements within a gene. Genes contain most of the information necessary for living cells to survive and reproduce. [ 1 ] [ 2 ] In most organisms, genes are made of DNA, where the particular DNA sequence determines the function of the gene.

  6. Complementarity-determining region - Wikipedia

    en.wikipedia.org/wiki/Complementarity...

    Complementarity-determining regions (CDRs) are polypeptide segments of the variable chains in immunoglobulins (antibodies) and T cell receptors, generated by B-cells and T-cells respectively. CDRs are where these molecules bind to their specific antigen and their structure/sequence determines the binding activity of the respective antibody.

  7. Terminal deoxynucleotidyl transferase - Wikipedia

    en.wikipedia.org/wiki/Terminal_deoxynucleotidyl...

    1791 21673 Ensembl ENSG00000107447 ENSMUSG00000025014 UniProt P04053 P09838 RefSeq (mRNA) NM_001017520 NM_004088 NM_001043228 NM_009345 RefSeq (protein) NP_001017520 NP_004079 NP_001036693 NP_033371 Location (UCSC) Chr 10: 96.3 – 96.34 Mb Chr 19: 41.02 – 41.05 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Terminal deoxynucleotidyl transferase (TdT), also known as DNA ...

  8. Recombination-activating gene - Wikipedia

    en.wikipedia.org/wiki/Recombination-activating_gene

    Current studies have indicated that RAG-1 and RAG-2 must work in a synergistic manner to activate VDJ recombination. RAG-1 was shown to inefficiently induce recombination activity of the VDJ genes when isolated and transfected into fibroblast samples. When RAG-1 was cotransfected with RAG-2, recombination frequency increased by a 1000-fold. [3]

  9. Susumu Tonegawa - Wikipedia

    en.wikipedia.org/wiki/Susumu_Tonegawa

    Susumu Tonegawa (利根川 進, Tonegawa Susumu, born September 5, 1939) is a Japanese scientist who was the sole recipient of the Nobel Prize for Physiology or Medicine in 1987 for his discovery of V(D)J recombination, the genetic mechanism which produces antibody diversity. [1]