Shaw J P, Utz P J, Durand D B, Toole J J, Emmel E A, Crabtree G R
Howard Hughes Medical Institute, Stanford University, CA 94305.
Science. 1988 Jul 8;241(4862):202-5. doi: 10.1126/science.3260404.
Molecules involved in the antigen receptor-dependent regulation of early T cell activation genes were investigated with the use of functional sequences of the T cell activation-specific enhancer of interleukin-2 (IL-2). One of these sequences forms a protein complex, NFAT-1, specifically with nuclear extracts of activated T cells. This complex appeared 10 to 25 minutes before the activation of the IL-2 gene. Studies with inhibitors of protein synthesis indicated that the time of synthesis of the activator of the IL-2 gene in Jurkat T cells corresponds to the time of appearance of NFAT-1. NFAT-1, or a very similar protein, bound functional sequences of the long terminal repeat (LTR) of the human immunodeficiency virus type 1; the LTR of this virus is known to be stimulated during early T cell activation. The binding site for this complex activated a linked promoter after transfection into antigen receptor-activated T cells but not other cell types. These characteristics suggest that NFAT-1 transmits signals initiated at the T cell antigen receptor.
利用白细胞介素-2(IL-2)的T细胞活化特异性增强子的功能序列,对参与早期T细胞活化基因的抗原受体依赖性调控的分子进行了研究。其中一个序列与活化T细胞的核提取物特异性形成一种蛋白质复合物,即NFAT-1。这种复合物在IL-2基因活化前10到25分钟出现。蛋白质合成抑制剂的研究表明,Jurkat T细胞中IL-2基因激活剂的合成时间与NFAT-1出现的时间相对应。NFAT-1或一种非常相似的蛋白质与1型人类免疫缺陷病毒长末端重复序列(LTR)的功能序列结合;已知这种病毒的LTR在早期T细胞活化过程中受到刺激。该复合物的结合位点在转染到抗原受体活化的T细胞而非其他细胞类型后激活了相连的启动子。这些特征表明NFAT-1传递在T细胞抗原受体处启动的信号。