Malissen M, McCoy C, Blanc D, Trucy J, Devaux C, Schmitt-Verhulst A M, Fitch F, Hood L, Malissen B
Nature. 1986;319(6048):28-33. doi: 10.1038/319028a0.
A germline T-cell receptor variable region (V beta) gene segment (V beta 14) has been mapped 10 kilobases to the 3' side of the constant region (C beta 2) gene. The V beta 14 gene segment is in an inverted transcriptional polarity relative to the diversity-region (D beta) and joining-region (J beta) gene segments and the C beta genes. Analyses of a T-cell clone (J 6.19), which has productively rearranged the V beta 14 gene segment, indicate that the productive V beta-D beta-J beta rearrangement and its reciprocal flank recombination product are linked and located at either border of a chromosomal inversion. These data demonstrate for the first time a linkage between mammalian V and C genes and verify that a functional T-cell receptor V beta gene can be constructed through a chromosomal inversion.
一种种系T细胞受体可变区(Vβ)基因片段(Vβ14)已被定位到恒定区(Cβ2)基因3'端10千碱基处。Vβ14基因片段相对于多样性区(Dβ)和连接区(Jβ)基因片段以及Cβ基因,其转录极性是反向的。对一个已有效重排Vβ14基因片段的T细胞克隆(J 6.19)的分析表明,有效的Vβ-Dβ-Jβ重排及其反向侧翼重组产物是相连的,且位于染色体倒位的任一边界处。这些数据首次证明了哺乳动物V基因和C基因之间的联系,并证实功能性T细胞受体Vβ基因可通过染色体倒位构建。