Sun J, Rose J B, Bird P
Department of Medicine, Monash Medical School, Clive Ward Centre, Box Hill Hospital, Australia.
J Biol Chem. 1995 Jul 7;270(27):16089-96. doi: 10.1074/jbc.270.27.16089.
Human proteinase inhibitor 6 (PI-6) is a recently described protein belonging to the serine proteinase inhibitor (serpin) superfamily. Sequence similarity suggests that PI-6 most resembles the ovalbumin (ov) serpins which include plasminogen activator inhibitor-2, the squamous cell carcinoma antigen, monocyte/neutrophil elastase inhibitor, and maspin. Although these proteins are associated with carcinomas and inflammation, they appear to have diverse functions and little is known of their physiological roles. In this study we have characterized cDNA and genomic clones encoding mouse PI-6 in order to analyze the localization, structure, and expression of the gene. The reactive center residues (Arg-Cys) are conserved in the mouse molecule, and recombinant mouse PI-6 was shown to bind thrombin, indicating that it has similar inhibitory properties to its human counterpart. Using reverse transcriptase-polymerase chain reaction assays on RNA isolated from 15-day-old embryos and adult mice, we have shown that mouse PI-6 expression is developmentally regulated, and that, unlike human PI-6, it is absent from the placenta. The mouse homologue of the human PI-6 gene has been designated Spi3 and was mapped to chromosome 13 between the Pl1 and ctla2 alpha genes. It spans 20 kilobases, consists of 7 exons and 6 introns, and contains a TATA motif 24 nucleotides upstream of the transcriptional start site. A 680-base pair DNA fragment containing this motif and 31 nucleotides of the 5'-untranslated region of the structural gene directed transcription of a bacterial cat gene, demonstrating the presence of a functional promoter. The PI-6 gene lacks an intron present in the ovalbumin and PAI-2 genes; otherwise it is identical in terms of the numbers, position, and phasing of the intron/exon boundaries. These results suggest that PI-6 and the ov-serpin genes have diverged and do not belong to the same subgroup.
人蛋白酶抑制剂6(PI-6)是最近描述的一种属于丝氨酸蛋白酶抑制剂(丝氨酸蛋白酶抑制剂)超家族的蛋白质。序列相似性表明,PI-6与卵清蛋白(ov)丝氨酸蛋白酶抑制剂最为相似,其中包括纤溶酶原激活物抑制剂-2、鳞状细胞癌抗原、单核细胞/中性粒细胞弹性蛋白酶抑制剂和maspin。尽管这些蛋白质与癌症和炎症相关,但它们似乎具有多种功能,而对其生理作用知之甚少。在本研究中,我们对编码小鼠PI-6的cDNA和基因组克隆进行了表征,以分析该基因的定位、结构和表达。反应中心残基(精氨酸-半胱氨酸)在小鼠分子中是保守的,并且重组小鼠PI-6被证明能结合凝血酶,这表明它具有与其人类对应物相似的抑制特性。通过对从15日龄胚胎和成年小鼠分离的RNA进行逆转录-聚合酶链反应分析,我们发现小鼠PI-6的表达受发育调控,并且与人类PI-6不同,它在胎盘中不存在。人PI-6基因的小鼠同源物已被命名为Spi3,并被定位到13号染色体上Pl1和ctla2α基因之间。它跨度为20千碱基,由7个外显子和6个内含子组成,并且在转录起始位点上游24个核苷酸处含有一个TATA基序。一个包含该基序和结构基因5'-非翻译区31个核苷酸的680碱基对DNA片段指导细菌cat基因的转录,证明存在一个功能性启动子。PI-6基因缺乏卵清蛋白和PAI-2基因中存在的一个内含子;否则,它在内含子/外显子边界的数量、位置和相位方面是相同的。这些结果表明PI-6和ov-丝氨酸蛋白酶抑制剂基因已经分化,不属于同一亚组。