Geraghty D E, Wei X H, Orr H T, Koller B H
Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis 55455.
J Exp Med. 1990 Jan 1;171(1):1-18. doi: 10.1084/jem.171.1.1.
We describe here the isolation and sequencing of a previously uncharacterized HLA class I gene. This gene, HLA-5.4, is the third non-HLA-A,B,C gene characterized whose sequence shows it encodes an intact class I protein. RNase protection assays with a probe specific for this gene demonstrated its expression in B lymphoblastoid cell lines, in resting T cells, and skin cells, while no mRNA could be detected in the T cell line Molt 4. Consistent with a pattern of expression different from that of other class I genes, DNA sequence comparisons identified potential regulator motifs unique to HLA-5.4 and possibly essential for tissue-specific expression. Protein sequence analysis of human and murine class I antigens has identified 10 highly conserved residues believed to be involved in antigen binding. Five of these are altered in HLA-5.4, and of these, three are nonconservative. In addition, examination of the HLA-5.4 DNA sequence predicts that the cytoplasmic segment of this protein is shorter than that of the classical transplantation antigens. The 3' untranslated region of the HLA-5.4 gene contains one member of a previously undescribed multigene family consisting of at least 30 members. Northern analysis showed that several of these sequences were transcribed, and the most ubiquitous transcript, a 600-nucleotide polyadenylated mRNA, was found in all tissues and cells examined. This sequence is conserved in the mouse genome, where a similar number of copies were found, and one of these sequences was also transcribed, yielding a 600-nucleotide mRNA. The characterization of this unique HLA class I gene and the demonstration of its tissue-specific expression have prompted us to propose that HLA-5.4 be designated HLA-F.
我们在此描述了一个此前未被鉴定的HLA I类基因的分离和测序情况。该基因,即HLA-5.4,是第三个被鉴定的非HLA-A、B、C基因,其序列显示它编码一种完整的I类蛋白。用针对该基因的特异性探针进行的核糖核酸酶保护试验表明,它在B淋巴母细胞系、静息T细胞和皮肤细胞中表达,而在T细胞系Molt 4中未检测到mRNA。与其他I类基因不同的表达模式一致,DNA序列比较确定了HLA-5.4特有的潜在调控基序,可能对组织特异性表达至关重要。对人和鼠I类抗原的蛋白质序列分析确定了10个高度保守的残基,据信它们参与抗原结合。其中5个在HLA-5.4中发生了改变,其中3个是非保守性的。此外,对HLA-5.4 DNA序列的检查预测该蛋白的细胞质区段比经典移植抗原的要短。HLA-5.4基因的3'非翻译区包含一个此前未描述的多基因家族的一个成员,该家族至少有30个成员。Northern分析表明,这些序列中有几个被转录,在所有检测的组织和细胞中都发现了最普遍的转录本,即一个600个核苷酸的多聚腺苷酸化mRNA。该序列在小鼠基因组中是保守的,在那里发现了类似数量的拷贝,其中一个序列也被转录,产生一个600个核苷酸的mRNA。这个独特的HLA I类基因的特征及其组织特异性表达的证明促使我们提议将HLA-5.4命名为HLA-F。