TY - JOUR
T1 - Sequences and repertoire of the human T cell receptor α and β chain variable region genes in thymocytes
AU - Kimura, Nobuhiro
AU - Toyonaga, Barry
AU - Yoshikai, Yasunobu
AU - Du, Ran‐Pan ‐P
AU - Mak, Tak W.
PY - 1987/1/1
Y1 - 1987/1/1
N2 - To compare and contrast the human T cell antigen receptor (TcR) α and β chain messages found in human thymocytes to those previously isolated from human peripheral blood T lymphocytes and other nonthymic sources, 13 TcR α and 13 TcR β cDNA were isolated from a human thymocyte library and the nucleotide sequences were determined. The data indicate that, as was found in the peripheral T lymphocytes, the majority of the TcR α and TcRβ chain thymocyte cDNA were derived from potentially functional messages. Although the thymocyte‐derived TcR cDNA do not contain any unique structural features when compared to TcR cDNA from mature T lymphocytes, 4 new Jα segments, 17 new V‐gene segments (9 Vα; 8 Vβ) and 7 additional V‐gene families (4 Vα and 3 Vβ) and sequences had been identified. The exon CβO, found in many murine thymocyte TcR β messages, was not found in over 75 human β chain messages. Based on these new data, a revised estimate of human TcR Vα, Jα and Vβ repertoires is calculated. The most significant change has been the increase in the estimated number of human TcR Vβ‐gene segments to a total of about 100 distributed among about 18 families. The Vα families are now revised upward to 16, with a total number of Vα segments of 50. The estimate of the Jα segments in humans remains between 50–100.
AB - To compare and contrast the human T cell antigen receptor (TcR) α and β chain messages found in human thymocytes to those previously isolated from human peripheral blood T lymphocytes and other nonthymic sources, 13 TcR α and 13 TcR β cDNA were isolated from a human thymocyte library and the nucleotide sequences were determined. The data indicate that, as was found in the peripheral T lymphocytes, the majority of the TcR α and TcRβ chain thymocyte cDNA were derived from potentially functional messages. Although the thymocyte‐derived TcR cDNA do not contain any unique structural features when compared to TcR cDNA from mature T lymphocytes, 4 new Jα segments, 17 new V‐gene segments (9 Vα; 8 Vβ) and 7 additional V‐gene families (4 Vα and 3 Vβ) and sequences had been identified. The exon CβO, found in many murine thymocyte TcR β messages, was not found in over 75 human β chain messages. Based on these new data, a revised estimate of human TcR Vα, Jα and Vβ repertoires is calculated. The most significant change has been the increase in the estimated number of human TcR Vβ‐gene segments to a total of about 100 distributed among about 18 families. The Vα families are now revised upward to 16, with a total number of Vα segments of 50. The estimate of the Jα segments in humans remains between 50–100.
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U2 - 10.1002/eji.1830170312
DO - 10.1002/eji.1830170312
M3 - Article
C2 - 3494611
AN - SCOPUS:0023265665
SN - 0014-2980
VL - 17
SP - 375
EP - 383
JO - European Journal of Immunology
JF - European Journal of Immunology
IS - 3
ER -