Kronenberg M, Goverman J, Haars R, Malissen M, Kraig E, Phillips L, Delovitch T, Suciu-Foca N, Hood L
Nature. 1985;313(6004):647-53. doi: 10.1038/313647a0.
Rearrangements of T-cell receptor beta-chain genes are usually found on both chromosomal homologues, occurring by both deletional and non-deletional mechanisms. Two constant-region (C beta) genes have been identified previously and at least one is transcribed in every helper or cytotoxic T cell tested, but the choice of C beta gene expression is not correlated with the specialized functions of these T lymphocytes. By contrast, four of five suppressor T-cell hybridomas examined have deleted all known joining (J beta) gene segments and C beta genes and therefore may have antigen receptors encoded by different T-cell receptor gene families.
T细胞受体β链基因重排通常在两条染色体同源物上均有发现,通过缺失和非缺失机制发生。先前已鉴定出两个恒定区(Cβ)基因,并且在每个测试的辅助性或细胞毒性T细胞中至少有一个被转录,但Cβ基因表达的选择与这些T淋巴细胞的特殊功能无关。相比之下,所检测的五个抑制性T细胞杂交瘤中有四个已缺失了所有已知的连接(Jβ)基因片段和Cβ基因,因此可能具有由不同T细胞受体基因家族编码的抗原受体。