Watanabe T, Yonekura H, Terazono K, Yamamoto H, Okamoto H
Department of Biochemistry, Tohoku University School of Medicine, Miyagi, Japan.
J Biol Chem. 1990 May 5;265(13):7432-9.
We previously identified a novel gene, reg (i.e. regenerating gene), in the screening of a rat regenerating islet-derived cDNA library, and isolated its human cDNA homologue which encodes a 166-amino acid protein (Terazono, K., Yamamoto, H., Takasawa, S., Shiga, K., Yonemura, Y., Tochino, Y., and Okamoto, H. (1988) J. Biol. Chem. 263, 2111-2114). In the present study, we have isolated the human reg gene, determined its complete nucleotide sequence, and examined its expression in human tissues. The functional human reg gene is a single copy gene, spans approximately 3.0 kilobase pairs, and is composed of six exons and five introns. TATA box and CCAAT box-like sequences are located at 27 and 100 base pairs upstream from the transcriptional initiation site. The human reg mRNA was detected predominantly in the pancreas, and at lower levels in the gastric mucosa and the kidney. Furthermore, the reg gene was found to be expressed ectopically in colon and rectal tumors. Immunoblot analysis demonstrated several molecular forms (15-18 kDa) of the reg protein in the pancreas. The 166-amino acid sequence encoded by the human reg gene contains the 144-amino acid sequence of pancreatic stone protein determined by De Caro et al. (De Caro, A. M., Adrich, Z., Fournet, B., Capon, C., Bonicel, J. J., De Caro, J. D., and Rovery, M. (1989) Biochim. Biophys. Acta 994, 281-284) and the partially determined 45-amino acid sequence of pancreatic thread protein (Gross, J., Carlson, R. I., Brauer, A. W., Margolies, M. N., Warshaw, A. L., and Wands, J. R. (1985) J. Clin. Invest. 76, 2115-2126), indicating that the reg protein, pancreatic stone protein, and pancreatic thread protein are simply different names for a single protein deriving from the reg gene.
我们先前在筛选大鼠再生胰岛衍生的cDNA文库时鉴定出一个新基因reg(即再生基因),并分离出其人类cDNA同源物,该同源物编码一种166个氨基酸的蛋白质(寺园,K.,山本,H.,高泽,S.,志贺,K.,米村,Y.,户知野,Y.,以及冈本,H.(1988年)《生物化学杂志》263卷,2111 - 2114页)。在本研究中,我们分离出了人类reg基因,确定了其完整的核苷酸序列,并检测了它在人体组织中的表达。功能性人类reg基因是一个单拷贝基因,跨度约为3.0千碱基对,由六个外显子和五个内含子组成。TATA盒和类似CCAAT盒的序列位于转录起始位点上游27和100个碱基对处。人类reg mRNA主要在胰腺中检测到,在胃黏膜和肾脏中的水平较低。此外,发现reg基因在结肠和直肠肿瘤中异位表达。免疫印迹分析表明胰腺中存在几种分子形式(15 - 18 kDa)的reg蛋白。人类reg基因编码的166个氨基酸序列包含由德卡罗等人确定的胰腺结石蛋白的144个氨基酸序列(德卡罗,A.M.,阿德里奇,Z.,富尔内,B.,卡蓬,C.,博尼塞尔,J.J.,德卡罗,J.D.,以及罗韦里,M.(1989年)《生物化学与生物物理学报》994卷,281 - 284页)以及部分确定的胰腺丝蛋白的45个氨基酸序列(格罗斯,J.,卡尔森,R.I.,布劳尔,A.W.,马戈利斯,M.N.,沃肖,A.L.,以及万兹,J.R.(1985年)《临床研究杂志》76卷,2115 - 2126页),这表明reg蛋白、胰腺结石蛋白和胰腺丝蛋白只是源自reg基因的单一蛋白质的不同名称。