T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC) . Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell , the T cell receptor loci are rearranged and expressed in the order delta , gamma , beta , and alpha. If both delta and gamma rearrangements produce functional chains , the cell expresses delta and gamma. If not , the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable) , J (joining) , and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus , between the alpha V and J segments. During T cell development , the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains , the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity , resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments of the alpha locus are known to be incapable of encoding a protein and are considered pseudogenes. [provided by RefSeq , Aug 2016] ,
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