Hennessy S W, Frazier B A, Kim D D, Deckwerth T L, Baumgartel D M, Rotwein P, Frazier W A
Department of Biological Chemistry, Washington University School of Medicine, St. Louis, Missouri 63110.
J Cell Biol. 1989 Feb;108(2):729-36. doi: 10.1083/jcb.108.2.729.
The nucleotide sequence of human thrombospondin (TS) mRNA has been determined from human fibroblast and endothelial cDNAs. The sequence of 5802 bp begins 110 bp upstream from the initiator codon and includes the entire 3' untranslated region (UTR) of the mRNA. The coding region (3510 bp) specifies a protein of 1170 amino acids with all of the known features of the TS subunit (Frazier, W. A. 1987. J. Cell Biol. 105:625-632). The long 3' UTR of 2166 nucleotides is extremely A/T-rich, particularly in the latter half. It contains 37 TATT or ATTT(A) sequences that have been suggested as mediators of the stability of mRNAs for cytokines, lymphokines, and oncogenes (Shaw, G., and R. Kamen. 1986. Cell. 46:659-667). Another unusual feature of the 3' UTR of TS mRNA is a stretch of 42 nucleotides of which 40 are thymidines (uridine in the mRNA) including an uninterrupted sequence of 26 thymidines. This region is flanked by two sets of direct repeats suggesting that it may be an insertion element of retrotranscriptional origin. Comparison of the 3' untranslated region of TS mRNA with the GenBank data base indicates the greatest degree of similarity with an alpha-interferon gene which contains a number of the TATT/ATTT consensus sites. The degree of similarity between the TS and interferon sequences is the same in regions of the interferon gene corresponding to its coding and noncoding regions suggesting that most of the TS 3' UTR may be derived from an interferon gene or pseudogene. The features of the TS mRNA 3' UTR provide a potential explanation for the rapid regulation of TS message observed in cultured cells in response to PDGF and suggest that TS is a member of a group of proteins which are intimately involved in the control of cell growth and differentiation.
已从人成纤维细胞和内皮细胞的cDNA中确定了人血小板反应蛋白(TS)mRNA的核苷酸序列。5802 bp的序列起始于起始密码子上游110 bp处,包括mRNA完整的3'非翻译区(UTR)。编码区(3510 bp)指定了一个由1170个氨基酸组成的蛋白质,具有TS亚基的所有已知特征(弗雷泽,W.A. 1987。《细胞生物学杂志》105:625 - 632)。2166个核苷酸的长3'UTR富含A/T,尤其是在后半部分。它包含37个TATT或ATTT(A)序列,这些序列被认为是细胞因子、淋巴因子和癌基因mRNA稳定性的介导因子(肖,G.,和R. 卡门。1986。《细胞》。46:659 - 667)。TS mRNA 3'UTR的另一个不寻常特征是一段42个核苷酸的序列,其中40个是胸苷(mRNA中的尿苷),包括一段26个胸苷的不间断序列。该区域两侧有两组直接重复序列,表明它可能是逆转录起源的插入元件。将TS mRNA的3'非翻译区与GenBank数据库进行比较,发现与α - 干扰素基因的相似程度最高,该基因包含许多TATT/ATTT共有位点。TS和干扰素序列之间的相似程度在干扰素基因对应其编码区和非编码区的区域是相同的,这表明TS的大部分3'UTR可能来源于一个干扰素基因或假基因。TS mRNA 3'UTR的特征为在培养细胞中观察到的TS信息对血小板衍生生长因子(PDGF)的快速调节提供了一个潜在的解释,并表明TS是一组紧密参与细胞生长和分化控制的蛋白质成员之一。