Hasegawa H, Utsunomiya Y, Kishimoto K, Yanagisawa K, Fujita S
First Department of Internal Medicine, Ehime University School of Medicine, Shigenobu, Japan.
J Virol. 1996 May;70(5):3258-63. doi: 10.1128/JVI.70.5.3258-3263.1996.
A novel cellular gene termed SFA-1 was isolated by differential hybridization of a cDNA library, using probes obtained from an adult T-cell leukemia cell line in comparison with probes obtained from normal CD4+ T cells and the MOLT-4 cell line. The mRNA of the SFA-1 gene is approximately 1.6 kb in size and encodes a protein of 253 amino acids, containing four putative transmembrane domains, a number of cysteine residues, and one potential N-glycosylation site in a major hydrophilic region between the third and fourth transmembrane domains. Expression of the SFA-1 gene was either absent or present at a low level in lymphoid cells but was up-regulated after transformation by human T-cell leukemia virus type 1 and transactivated by Tax. SFA-1 was broadly expressed in many human cell types and conserved in different species. Computer-aided comparison showed that SFA-1 had significant sequence homology and common structural features with members of the transmembrane 4 superfamily. SFA-1 antigen was detected as a 29-kDa membrane protein by immunoblotting, using anti-SFA-1 monoclonal antibody.
通过cDNA文库的差异杂交,利用从成人T细胞白血病细胞系获得的探针与从正常CD4 + T细胞和MOLT-4细胞系获得的探针进行比较,分离出一种名为SFA-1的新型细胞基因。SFA-1基因的mRNA大小约为1.6 kb,编码一个由253个氨基酸组成的蛋白质,该蛋白质含有四个推定的跨膜结构域、多个半胱氨酸残基,并且在第三个和第四个跨膜结构域之间的一个主要亲水区域有一个潜在的N-糖基化位点。SFA-1基因在淋巴细胞中要么不存在表达,要么表达水平很低,但在被1型人类T细胞白血病病毒转化后会上调,并被Tax反式激活。SFA-1在许多人类细胞类型中广泛表达,并且在不同物种中保守。计算机辅助比较显示,SFA-1与跨膜4超家族成员具有显著的序列同源性和共同的结构特征。使用抗SFA-1单克隆抗体通过免疫印迹检测到SFA-1抗原为一种29 kDa的膜蛋白。