Houchins J P, Kricek F, Chujor C S, Heise C P, Yabe T, McSherry C, Bach F H
Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis 55455.
Immunogenetics. 1993;37(2):102-7. doi: 10.1007/BF00216832.
We reported previously the isolation of a cDNA clone, designated NKG5, encoding a secreted protein that is expressed only in natural killer and T cells and is strongly upregulated upon cell activation. In this report we have isolated the NKG5 gene from a human placental genomic library and sequenced the gene and two kilobases of 5'-flanking DNA. Comparison with the cDNA sequence reveals that the NKG5 gene consists of five exons and four introns. Intron 1 contains a DNA segment that was reported to occur as an exon in 519, a closely related cDNA clone that was isolated from a T-cell library. This result indicates that NKG5 and 519 are alternative splicing products of a single gene. The 5'-flanking region of the NKG5 gene was analyzed for homology with the promoter regions of cytokines and other activation-induced genes showing lymphocyte-specific expression. Several segments displaying sequence similarity were identified. We also identified numerous sequence elements that have strong similarity to known binding sites for transcriptional regulatory proteins including T cell-specific and activation-specific regulatory factors. These findings are consistent with the cell-specific expression and the tight regulatory control that is observed for the NKG5 gene.
我们先前报道了一个名为NKG5的cDNA克隆的分离,它编码一种仅在自然杀伤细胞和T细胞中表达的分泌蛋白,并且在细胞激活时强烈上调。在本报告中,我们从人胎盘基因组文库中分离出NKG5基因,并对该基因和5'侧翼DNA的两个千碱基进行了测序。与cDNA序列的比较表明,NKG5基因由五个外显子和四个内含子组成。内含子1包含一个DNA片段,据报道该片段在519中作为外显子出现,519是从T细胞文库中分离出的一个密切相关的cDNA克隆。这一结果表明NKG5和519是单个基因的可变剪接产物。对NKG5基因的5'侧翼区域进行分析,以寻找与细胞因子和其他显示淋巴细胞特异性表达的激活诱导基因的启动子区域的同源性。鉴定出了几个显示序列相似性的片段。我们还鉴定出许多与转录调节蛋白的已知结合位点具有高度相似性的序列元件,包括T细胞特异性和激活特异性调节因子。这些发现与NKG5基因的细胞特异性表达和严格的调控控制是一致的。