Letourneur F, Malissen B
Centre d'Immunologie INSERM-CNRS de Marseille, Luminy, France.
Eur J Immunol. 1989 Dec;19(12):2269-74. doi: 10.1002/eji.1830191214.
We have isolated a variant of the DO-11.10.7 mouse T cell hybridoma which does not express functional T cell receptor alpha/beta chains. This variant, denoted 58 alpha-beta-, can be used as a recipient for T cell receptor alpha/beta gene transfer experiments to obtain cell lines which express only the products of the transfected alpha/beta genes at their surfaces. In the process of characterizing the defects affecting the 58 alpha-beta-T cell receptor genes, we have found that the parental BW5147 thymoma has undergone a previously unnoticed V alpha-J alpha rearrangement. This alpha rearrangement involves a V alpha pseudogene segment and accounts for the high level of alpha-mRNA transcripts present in the BW5147 alpha-beta- variant. Knowledge of the existence of this second, albeit nonfunctional, alpha-mRNA in BW5147 is of importance, since it could be, and actually already has been, mistakenly identified (due to partial nucleotide sequencing) in T hybrids as a functionally significant message donated by the normal T cell parent.
我们分离出了DO-11.10.7小鼠T细胞杂交瘤的一个变体,该变体不表达功能性T细胞受体α/β链。这个变体,记为58α-β-,可作为T细胞受体α/β基因转移实验的受体,以获得仅在其表面表达转染的α/β基因产物的细胞系。在表征影响58α-β-T细胞受体基因的缺陷的过程中,我们发现亲本BW5147胸腺瘤发生了一个先前未被注意到的Vα-Jα重排。这种α重排涉及一个Vα假基因片段,并解释了BW5147α-β-变体中存在的高水平α-mRNA转录本。了解BW5147中这种第二种(尽管无功能)α-mRNA的存在很重要,因为它可能已经并且实际上已经被(由于部分核苷酸测序)在T杂交瘤中错误地鉴定为正常T细胞亲本提供的功能上重要的信息。