Ignatowicz L, Kappler J W, Marrack P, Scherer M T
Howard Hughes Medical Institute, Department of Medicine, National Jewish Center for Immunology and Respiratory Medicine, Denver, CO 80206.
J Immunol. 1994 Jan 1;152(1):65-71.
The commonly used strains of laboratory mice have mouse mammary tumor viruses (MTV) integrated at various locations in their DNA. The number and position of these integrants varies from one strain of mouse to another. It has recently been shown that the genomes of many of the MTV code for superantigens. The predicted amino acid sequences of these superantigens and their specificity for TCR V beta differs for each MTV integrant. This study contains the predicted amino acid sequence and V beta specificity of two MTV superantigens that had not previously been analyzed. The results show that both of these MTV superantigens are specific for TCR that bear V beta 7, but unlike the MTV7 superantigen not for receptors bearing V beta 6 or V beta 8.1. The data also support the conclusion of previous studies that the COOH-terminal sequence of these proteins is a major factor in controlling their V beta reactivity.
常用的实验室小鼠品系在其DNA的不同位置整合有小鼠乳腺肿瘤病毒(MTV)。这些整合体的数量和位置因小鼠品系而异。最近有研究表明,许多MTV的基因组编码超抗原。这些超抗原的预测氨基酸序列及其对TCR Vβ的特异性因每个MTV整合体而异。本研究包含了两种此前未分析过的MTV超抗原的预测氨基酸序列和Vβ特异性。结果表明,这两种MTV超抗原对携带Vβ7的TCR具有特异性,但与MTV7超抗原不同,它们对携带Vβ6或Vβ8.1的受体不具有特异性。这些数据也支持了先前研究的结论,即这些蛋白质的COOH末端序列是控制其Vβ反应性的主要因素。