The human T cell antigen receptor is encoded by variable, diversity, and joining gene segments that rearrange to generate a complete V gene

Cell. 1984 Jun;37(2):393-401. doi: 10.1016/0092-8674(84)90369-6.

Abstract

A cDNA clone YT35 , synthesized from poly(A)+ RNA of the human T cell tumor Molt 3, exhibits homology to the variable (V), joining (J), and constant (C) regions of immunoglobulin genes. We have isolated and sequenced the germ-line V and J gene segment counterparts to YT35 from a human cosmid library, and these failed to encode 14 nucleotides of the cDNA clone between the V and J regions. We postulate that these 14 nucleotides are encoded by a third gene segment analogous to the diversity (D) gene segments of immunoglobulin heavy chain genes. This T cell antigen receptor V gene appears to be assembled from three gene segments, V, D, and J, and accordingly most closely resembles immunoglobulin heavy chain V genes.

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Cell Line
  • Cloning, Molecular*
  • DNA / analysis
  • DNA Restriction Enzymes
  • Genes*
  • Humans
  • Leukemia, Lymphoid
  • Mutation
  • Plasmids
  • Poly A / genetics
  • Polymorphism, Genetic
  • RNA / genetics
  • RNA, Messenger
  • Receptors, Antigen, T-Cell / genetics*

Substances

  • RNA, Messenger
  • Receptors, Antigen, T-Cell
  • Poly A
  • RNA
  • DNA
  • DNA Restriction Enzymes

Associated data

  • GENBANK/K02545
  • GENBANK/K02546
  • GENBANK/K02547