Plunkett M L, David C S, Freed J H
J Immunol. 1981 Oct;127(4):1679-85.
Analysis of the tryptic peptides obtained from the Ia.7-positive, "I-E" antigens produced by 4 F1 combinations derived from strain A.TFR5 has provided biochemical confirmation that I-A/I-E gene complementation can occur in the transconfiguration. The data obtained support the concept that structural genes, as opposed to regulatory genes, are the essential elements involved in this complementation and support the assignment of the I-E subregion of strain A.TFR5 as I-Ek. The data support the following assignments of the genes encoding the E beta chains: B10.A(4R) as E beta k, B10.A(5R) as E beta b, and B10.HTT as E beta s. Finally, data are presented demonstrating that the E beta chain derived from the recombinant D2.GD strain partially differs from the E beta d chain derived from a conventional H-2d haplotype strain, B10.D2.
对从源自A.TFR5品系的4种F1组合产生的Ia.7阳性“I-E”抗原中获得的胰蛋白酶肽段进行分析,已提供了生化证据,证明I-A/I-E基因互补可发生在反式构型中。所获得的数据支持这样的概念,即与调节基因相反,结构基因是参与这种互补的基本要素,并支持将A.TFR5品系的I-E亚区指定为I-Ek。这些数据支持对编码Eβ链的基因进行以下指定:B10.A(4R)为Eβk,B10.A(5R)为Eβb,B10.HTT为Eβs。最后,给出的数据表明,源自重组D2.GD品系的Eβ链与源自常规H-2d单倍型品系B10.D2的Eβd链部分不同。