Orlicky D J, Nordeen S K
Department of Pathology, University of Colorado Cancer Center, University of Colorado Health Sciences Center, Denver 80262, USA.
Prostaglandins Leukot Essent Fatty Acids. 1996 Oct;55(4):261-8. doi: 10.1016/s0952-3278(96)90007-1.
The cDNA has been cloned for a protein which copurifies with and colocalizes with [3H]PGF2 alpha binding activity, yet differs from the previously cloned prostaglandin F2 alpha receptor. Polyclonal antibody, produced against one of two protein bands present in a highly purified preparation of [3H]PGF2 alpha binding activity isolated from pregnant bovine corpus luteum, was used to screen a rat ovary cDNA expression library. A single strongly positive clone was identified containing a 4 kilobase (kb) insert. Northern analysis using this cDNA as a probe revealed the expression of a 6 kb mRNA with a tissue distribution similar to that seen by immunohistochemical analysis with the polyclonal antibody. Tissues possessing the largest quantity of the protein's mRNA are reproductive tissues, lung, and heart. Directed cDNA synthesis was required to clone the 5' end of the cDNA. Verification that the correct cDNA was cloned is provided by alignment of the predicted protein's mature amino terminal amino acid sequence with sequence observed by protein sequencing. Translation of the predicted 879 amino acid open reading frame (ORF) suggests a protein structure exhibiting six glycosylated immunoglobulin type loops, one of which may either be membrane associated or may be the site of association with another protein, a transmembrane region, and a short, highly charged, carboxy terminal cytoplasmic tail. Based upon searches of the NIH and EMBL protein databanks, this is a unique protein. The FPRP mRNA is notable for a highly structured G,C rich 5' end and over 3 kb of 3' untranslated region (UTR) that includes 7 ATTTA 'destabilization sequences' and an 'inflammatory mediator'-like sequence. These characteristic sequences in the 3' UTR suggest that the mRNA is tightly regulated and may code for a protein that is functionally related to an inflammatory mediator. Functional studies in the accompanying report suggest a negative regulatory function for this protein. We suggest the name prostaglandin F2 alpha receptor regulatory protein (FPRP).
已克隆出一种蛋白质的cDNA,该蛋白质与[3H]PGF2α结合活性共纯化并共定位,但与先前克隆的前列腺素F2α受体不同。用针对从怀孕牛黄体中分离出的[3H]PGF2α结合活性的高度纯化制剂中存在的两条蛋白带之一产生的多克隆抗体,筛选大鼠卵巢cDNA表达文库。鉴定出一个单一的强阳性克隆,其含有一个4千碱基(kb)的插入片段。用该cDNA作为探针进行Northern分析,揭示了一个6 kb mRNA的表达,其组织分布与用多克隆抗体进行免疫组织化学分析所见相似。拥有该蛋白质mRNA数量最多的组织是生殖组织、肺和心脏。需要进行定向cDNA合成来克隆cDNA的5'端。通过将预测蛋白质的成熟氨基末端氨基酸序列与蛋白质测序观察到的序列进行比对,证实克隆的是正确的cDNA。预测的879个氨基酸开放阅读框(ORF)的翻译表明,该蛋白质结构具有六个糖基化的免疫球蛋白类型环,其中一个可能与膜相关,或者可能是与另一种蛋白质结合的位点、一个跨膜区域以及一个短的、高度带电的羧基末端细胞质尾巴。基于对美国国立卫生研究院(NIH)和欧洲分子生物学实验室(EMBL)蛋白质数据库的搜索,这是一种独特的蛋白质。FPRP mRNA以其高度结构化的富含G、C的5'端和超过3 kb的3'非翻译区(UTR)为显著特征,该3'非翻译区包括7个ATTTA“不稳定序列”和一个“炎症介质”样序列。3'UTR中的这些特征序列表明该mRNA受到严格调控,可能编码一种与炎症介质功能相关的蛋白质。随附报告中的功能研究表明该蛋白质具有负调控功能。我们建议将其命名为前列腺素F2α受体调节蛋白(FPRP)。