Maquat L E, Chilcote R, Ryan P M
J Biol Chem. 1985 Mar 25;260(6):3748-53.
Nine cDNA clones of human adult liver triosephosphate (TP) isomerase have been isolated and characterized. All nine appear to be derived from a single mRNA species. DNA sequencing of one clone, designated pHTPI-5a, defined the last two nucleotides of the methionine initiation codon, the entire 744-nucleotide coding region of the mature polypeptide, and the entire 448-nucleotide 3' untranslated region. The frequency of TP isomerase clones in the cDNA library suggests that TP isomerase mRNA is present in adult liver at approximately 25 copies/cell. A single, low abundance TP isomerase mRNA species was detected in RNA isolated from normal human fibroblast cell lines. Analysis of TP isomerase mRNA levels in cultured fibroblasts of individuals that are homozygous for TP isomerase deficiency revealed normal levels in one and approximately 40% of normal levels in another. From this small patient sampling, it can be concluded that the genetic basis for TP isomerase deficiency is heterogeneous.
已分离并鉴定出9个人成体肝脏磷酸丙糖(TP)异构酶的cDNA克隆。所有9个克隆似乎都源自单一的mRNA种类。对一个名为pHTPI-5a的克隆进行DNA测序,确定了甲硫氨酸起始密码子的最后两个核苷酸、成熟多肽的整个744个核苷酸的编码区以及整个448个核苷酸的3'非翻译区。cDNA文库中TP异构酶克隆的频率表明,TP异构酶mRNA在成体肝脏中的含量约为每个细胞25个拷贝。在从正常人成纤维细胞系分离的RNA中检测到单一的、低丰度的TP异构酶mRNA种类。对TP异构酶缺乏纯合子个体的培养成纤维细胞中TP异构酶mRNA水平的分析显示,其中一个个体的水平正常,另一个个体的水平约为正常水平的40%。从这个小样本患者中可以得出结论,TP异构酶缺乏的遗传基础是异质性的。