Rytkönen-Nissinen M, Hurwitz J L, Pelkonen S, Levelt C, Pelkonen J
Department of Clinical Microbiology, University of Kuopio, Finland.
Eur J Immunol. 1999 Jul;29(7):2288-96. doi: 10.1002/(SICI)1521-4141(199907)29:07<2288::AID-IMMU2288>3.0.CO;2-1.
We have previously demonstrated that the onset of TCR alpha gene rearrangement is mainly restricted to the J alpha50 gene in fetal day 1delta thymocyte hybridomas. Now, J alpha50 rearrangements from fetal thymocyte hybridomas and from day 15.5 fetal thymus have been isolated and sequenced. We demonstrate that J alpha50 is rearranged to the rearranged Vdelta1 Ddelta2 gene segment. This indicates that the TCR alpha rearrangement process is initiated in fetal thymocytes far earlier than previously thought. These thymocytes have their delta genes still accessible for rearrangement and therefore, are controlled by the TCR delta enhancer (Edelta) (and/or another TCR delta specific cis-acting element). Our results further suggest that both Edelta and the TCR alpha enhancer (Ealpha) are active at the onset of alpha rearrangements or alternatively, the initial activation of the J alpha locus is controlled by Edelta. In addition, Vdelta1 Ddelta2 J alpha50 gene segments are replaced by secondary alpha rearrangements, indicating that thymocytes with the early alpha rearrangement are committed to the alphabeta lineage.
我们之前已经证明,在胚胎第1天的δ胸腺细胞杂交瘤中,TCRα基因重排的起始主要局限于Jα50基因。现在,已从胚胎胸腺细胞杂交瘤和胚胎第15.5天的胚胎胸腺中分离并测序了Jα50重排。我们证明Jα50重排至重排的Vδ1 Dδ2基因片段。这表明TCRα重排过程在胚胎胸腺细胞中起始的时间比之前认为的要早得多。这些胸腺细胞的δ基因仍可用于重排,因此,受TCRδ增强子(Edelta)(和/或另一个TCRδ特异性顺式作用元件)控制。我们的结果进一步表明,Edelta和TCRα增强子(Ealpha)在α重排起始时均有活性,或者,Jα基因座的初始激活受Edelta控制。此外,Vδ1 Dδ2 Jα50基因片段被二次α重排所取代,这表明具有早期α重排的胸腺细胞会定向分化为αβ谱系。