T细胞受体
胸腺细胞
生物
互补DNA
基因
cDNA文库
分子生物学
T细胞
T淋巴细胞
遗传学
外显子
基因重排
受体
CD8型
抗原
免疫系统
作者
Nobuhiro Kimura,Barry Toyonaga,Yasunobu Yoshikai,Ran‐Pan Du,Tak W. Mak
标识
DOI:10.1002/eji.1830170312
摘要
Abstract 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 J α segments, 17 new V‐gene segments (9 V α ; 8 Vβ) and 7 additional V‐gene families (4 V α and 3 Vβ) and sequences had been identified. The exon C β O, 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 V α , J α 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 V α families are now revised upward to 16, with a total number of V α segments of 50. The estimate of the J α segments in humans remains between 50–100.
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