Studer M, Terao M, Gianni M, Garattini E
Molecular Biology Unit, Centro Daniela e Catullo Borgomainerio, Istituto di Ricerche Farmacologiche, Mario Negri, Milano, Italy.
Biochem Biophys Res Commun. 1991 Sep 30;179(3):1352-60. doi: 10.1016/0006-291x(91)91722-o.
The second leader exon and the relative promoter of the mouse liver/bone/kidney-type alkaline phosphatase gene were identified and characterized. The transcription initiation site was determined by S1 mapping analysis. The differential expression of the two alternatively spliced transcripts was assessed in cell lines of different origin and in various tissues by polymerase chain reaction and RNase mapping analysis. The first promoter is active in embryo derived cells, whereas the second promoter is silent in basal conditions but it is activated by dibutyryl cAMP in fibroblastic cells. In the whole animal, the transcript driven by the first promoter is found in most tissues albeit at different levels, while the one driven by the second promoter is specifically expressed at high levels only in the heart.
鉴定并表征了小鼠肝/骨/肾型碱性磷酸酶基因的第二个主要外显子及其相关启动子。通过S1图谱分析确定了转录起始位点。通过聚合酶链反应和核糖核酸酶图谱分析,评估了两种可变剪接转录本在不同来源的细胞系和各种组织中的差异表达。第一个启动子在胚胎衍生细胞中具有活性,而第二个启动子在基础条件下是沉默的,但在成纤维细胞中可被二丁酰环磷腺苷激活。在整个动物体内,由第一个启动子驱动的转录本在大多数组织中都能找到,尽管水平不同,而由第二个启动子驱动的转录本仅在心脏中特异性高水平表达。