Ikeda M, Takemura T, Hino S, Yoshioka K
Department of Pediatrics, Kinki University School of Medicine, 377-2 Ohno-higashi, Osaka-sayama, 589, Japan.
Biochem Biophys Res Commun. 2000 Feb 5;268(1):225-30. doi: 10.1006/bbrc.2000.2103.
Tubulointerstitial nephritis antigen (TIN-ag) is an extracellular matrix basement protein which was originally identified as a target antigen involved in anti-tubular basement membrane (TBM) antibody-mediated interstitial nephritis (TIN). Further investigations elucidated that TIN-ag plays a role in renal tubulogenesis and that TIN-ag is defected in hereditary tubulointerstitial disorder such as juvenile nephronophthisis. We previously isolated and characterized 54 kDa glycoprotein as TIN-ag. cDNA encoding rabbit and mouse TIN-ag has recently been identified. In the present study, the cDNA of the human homologue of TIN-ag was cloned and its nucleotide sequence was determined (Accession No. AB022277; the DDBJ nucleotide sequence database). Deduced amino acid sequence (476 aa) exhibited the presence of a signal peptide (1-18 aa), cysteine residues termed follistatin module, six potential glycosylation sites, and an ATP/GTP-binding site. Homology search revealed approximately 85% homology with both rabbit and mouse TIN-ag, and also some ( approximately 40%) similarity with C. elegans. Human TIN-ag contained a sequence similar to several classes of extracellular matrix molecules in amino terminal region and to cathepsin family of cysteine proteinases in the carboxyl terminal region. Northern blot analysis revealed exclusive expression of this molecule in human adult and fetal kidney tissues. Using a monoclonal antibody recognizing human TIN-ag, protein expression ( approximately 50 kDa) was identified in cultured COS-1 cells transfected with human TIN-ag cDNA. The human TIN-ag was mapped to chromosome 6p11.2-12 by fluorescence in situ hybridization. These results may provide further evidence for understanding TIN-ag molecule and clues for gene analysis of juvenile nephronophthisis.
肾小管间质性肾炎抗原(TIN-ag)是一种细胞外基质基底蛋白,最初被鉴定为参与抗肾小管基底膜(TBM)抗体介导的间质性肾炎(TIN)的靶抗原。进一步研究表明,TIN-ag在肾小管生成中起作用,并且在诸如青少年肾单位肾痨等遗传性肾小管间质性疾病中存在缺陷。我们之前分离并鉴定了54 kDa糖蛋白为TIN-ag。最近已鉴定出编码兔和小鼠TIN-ag的cDNA。在本研究中,克隆了人类TIN-ag同源物的cDNA并确定了其核苷酸序列(登录号AB022277;DDBJ核苷酸序列数据库)。推导的氨基酸序列(476个氨基酸)显示存在信号肽(1-18个氨基酸)、称为卵泡抑素模块的半胱氨酸残基、六个潜在的糖基化位点和一个ATP/GTP结合位点。同源性搜索显示与兔和小鼠TIN-ag的同源性约为85%,与秀丽隐杆线虫也有一些(约40%)相似性。人类TIN-ag在氨基末端区域包含与几类细胞外基质分子相似的序列,在羧基末端区域与半胱氨酸蛋白酶的组织蛋白酶家族相似。Northern印迹分析显示该分子仅在人类成人和胎儿肾脏组织中表达。使用识别人类TIN-ag的单克隆抗体,在转染了人类TIN-ag cDNA的培养COS-1细胞中鉴定出蛋白质表达(约50 kDa)。通过荧光原位杂交将人类TIN-ag定位到6号染色体p11.2-12。这些结果可能为理解TIN-ag分子提供进一步证据,并为青少年肾单位肾痨的基因分析提供线索。