Gewert D R, Coulombe B, Castelino M, Skup D, Williams B R
EMBO J. 1987 Mar;6(3):651-7. doi: 10.1002/j.1460-2075.1987.tb04804.x.
A genomic clone encompassing the entire coding region of a murine gene homologous to human erythroid potentiating activity/tissue inhibitor of metalloproteinase (EPA/TIMP) was isolated and sequenced. Based on alignment with human EPA/TIMP cDNAs we deduce a structure comprising five exons and four introns extending over 4.3 kb of DNA. In mouse and hamster cell lines transcription from this gene and interferon genes is induced by Newcastle Disease virus (NDV). Examination of the 5'-flanking sequences of the gene reveals a set of repeated elements with structural similarity to those previously described as inducer-responsive elements in the human IFN-beta 1 gene. The 4.3-kb DNA fragment encompassing the homologous murine EPA/TIMP gene was transfected into human T98G cells and transfectants tested for NDV inducibility. In contrast to the endogenous human gene, the integrated murine EPA/TIMP gene was NDV-inducible and TIMP activity was detectable in the cell culture fluid.
分离并测序了一个基因组克隆,该克隆包含与人类红细胞生成增强活性/金属蛋白酶组织抑制剂(EPA/TIMP)同源的小鼠基因的整个编码区。基于与人类EPA/TIMP cDNA的比对,我们推断该结构由五个外显子和四个内含子组成,跨越4.3 kb的DNA。在小鼠和仓鼠细胞系中,新城疫病毒(NDV)可诱导该基因和干扰素基因的转录。对该基因5'侧翼序列的检查揭示了一组重复元件,其结构与先前在人类IFN-β1基因中描述为诱导剂反应元件的元件相似。将包含同源小鼠EPA/TIMP基因的4.3 kb DNA片段转染到人T98G细胞中,并检测转染子的NDV诱导性。与内源性人类基因相反,整合的小鼠EPA/TIMP基因具有NDV诱导性,并且在细胞培养液中可检测到TIMP活性。