Terao M, Studer M, Gianní M, Garattini E
Molecular Biology Unit, Centro Daniela e Catullo Borgomainerio, Istituto di Ricerche Farmacologiche Mario Negri, Milano, Italy.
Biochem J. 1990 Jun 15;268(3):641-8. doi: 10.1042/bj2680641.
The gene coding for the mouse alkaline phosphatase expressed in liver, bone, kidney and placenta (liver/bone/kidney-type alkaline phosphatase, L/B/K-ALP) was isolated and characterized. This gene consists of 12 exons and it is at least 49 kb long. The first two exons are separated by a long intron which is at least 32 kb in size, whereas the other exons span within the remaining 17 kb. Primer extension and S1-nuclease mapping analyses with placental mRNA demonstrate a single major transcription start site, which is preceded by a G + C-rich region containing a TATA-like sequence and three copies of the consensus binding site for the transcription factor Sp1. Transfection experiments using two different reporter genes show that the 5'-flanking region of the gene is active as a promoter in undifferentiated F9 teratocarcinoma cells, but not in 3T3 fibroblasts, consistent with the L/B/K-ALP mRNA level in the two cell lines. As expected from the sequence similarity at the cDNA level, the structural organization of the mouse gene is similar to that of the human and rat L/B/K-ALP genes, suggesting that they all derive from a single ancestral gene.
编码在肝脏、骨骼、肾脏和胎盘中表达的小鼠碱性磷酸酶(肝/骨/肾型碱性磷酸酶,L/B/K-ALP)的基因被分离并进行了表征。该基因由12个外显子组成,长度至少为49 kb。前两个外显子被一个至少32 kb大小的长内含子隔开,而其他外显子分布在其余的17 kb范围内。用胎盘mRNA进行的引物延伸和S1核酸酶图谱分析表明有一个主要的转录起始位点,其前面是一个富含G + C的区域,包含一个类似TATA的序列和转录因子Sp1的共有结合位点的三个拷贝。使用两种不同报告基因的转染实验表明,该基因的5'侧翼区域在未分化的F9畸胎瘤细胞中作为启动子具有活性,但在3T3成纤维细胞中则无活性,这与两种细胞系中L/B/K-ALP mRNA水平一致。正如从cDNA水平的序列相似性所预期的那样,小鼠基因的结构组织与人和大鼠的L/B/K-ALP基因相似,表明它们都源自一个单一的祖先基因。