Gahlmann R, Kedes L
Program in Molecular Biology and Genetics, University of Southern California School of Medicine, Los Angeles 90033.
J Biol Chem. 1990 Jul 25;265(21):12520-8.
The gene encoding human fast skeletal muscle troponin C (TnC) was cloned, mapped, and sequenced. The locations of intron positions in this gene were compared to those in the related genes for mouse slow skeletal TnC and vertebrate and nonvertebrate calmodulins. We detected strikingly similar purine-rich DNA sequences on the coding strand in the basal promoter of the genes for fast and slow troponin C and chicken calmodulin II which may represent conserved regulatory elements in genes of the vertebrate troponin C/calmodulin gene family. We mapped the transcriptional start site of the gene and analyzed the expression of TnC test genes in the myogenic cell lines C2, L8, and H9c2(2-1) and in the human fibroblast line HuT12. Constructs comprising 4.7 or 6.2 kilobase pairs of 5'-flanking sequence (including the genuine transcriptional start site) upstream of the chloramphenicol acetyltransferase gene as reporter expressed the hybrid gene in C2 cells but not in nonmuscle cells. Surprisingly, no expression was found in cell lines L8 and H9c2(2-1) despite the fact that all three muscle cell lines vigorously express the endogenous TnC fast mRNA after differentiation. The discrepancy between the expression of endogenous genes and the test gene in these cell lines indicates different requirements for regulatory elements in different myogenic cells.
编码人快速骨骼肌肌钙蛋白C(TnC)的基因被克隆、定位并测序。将该基因内含子位置与小鼠慢骨骼肌TnC以及脊椎动物和非脊椎动物钙调蛋白的相关基因中的内含子位置进行了比较。我们在快速和慢速肌钙蛋白C以及鸡钙调蛋白II基因的基础启动子的编码链上检测到了惊人相似的富含嘌呤的DNA序列,这些序列可能代表脊椎动物肌钙蛋白C/钙调蛋白基因家族基因中保守的调控元件。我们确定了该基因的转录起始位点,并分析了TnC测试基因在成肌细胞系C2、L8和H9c2(2-1)以及人成纤维细胞系HuT12中的表达。以氯霉素乙酰转移酶基因为报告基因,构建包含其5'侧翼序列4.7或6.2千碱基对(包括真正的转录起始位点)的构建体,该杂交基因在C2细胞中表达,但在非肌肉细胞中不表达。令人惊讶的是,尽管所有这三种肌肉细胞系在分化后都能强烈表达内源性快速TnC mRNA,但在L8和H9c2(2-1)细胞系中未发现表达。这些细胞系中内源性基因和测试基因表达之间的差异表明不同的成肌细胞对调控元件有不同的需求。