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Generation of this repertoire diversity is accomplished primarily through two mechanisms Gene translocation of the v (d)j genes is initiated when an enzyme called v (d)j recombinase recognizes recombination signal sequences located at the 3' end of v genes, the 5' end of j genes, and both ends of d genes. Recombination and somatic hypermutation (shm)
These two mechanisms produce massive diversity within antibody complementarity determining regions (cdrs), which form the primary antigen contact site. V (d)j gene recombination and somatic hypermutation (shm). Several complex genetic mechanisms have evolved that allow vertebrate b cells to generate a diverse pool of antibodies from a relatively small number of antibody genes.
First is the unpredictable recombination of gene segments that form the variable regions of immunoglobulin heavy and light chains, known as v (d)j recombination.
Among the mechanisms of antibody diversity include use of different variable (v), diversity (d) and joining (j) gene segments in the heavy chain and different v and j gene segments in the light chain There can also be differential pairing of heavy and light chain rearrangements. There are several molecular mechanisms in place that generate diversity within the hypervariable (hv) or complemntarity determining regions (cdrs) of an antibody molecule. Our body responds to various pathogens such as bacteria and viruses, producing a wide variety of antibodies that can bind to specific antigens
This is called the “diversity” of an antibody The diversity of antibodies is created by the combination of variable regions of h chains and l chains. The adaptive immune system of jawed vertebrates generates a highly diverse repertoire of antibodies to meet the antigenic challenges of a constantly evolving biological ecosystem Most of the diversity is generated by two mechanisms
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