Povinelli C M, Stewart J M, Knoll B J
Department of Pathology and Laboratory Medicine, Medical School, University of Texas Health Sciences Center, Houston.
Biochim Biophys Acta. 1992 Jan 23;1115(3):243-51. doi: 10.1016/0304-4165(92)90061-x.
Human heat stable alkaline phosphatases are encoded by two closely related genes: the PLAP-1, which specifies the term placental enzyme, and the PLAP-2, which is expressed primarily in germ cells. In the choriocarcioma line JEG-3, 8-Br-cAMP induced the accumulation of the mRNA of both genes, while sodium butyrate induced the accumulation of PLAP-2 transcripts only. Each agent increased the transcription rate of one or both of the genes, as assayed by run-on transcription. In transfection of JEG-3 cells with PLAP promoters fused to the firefly luciferase gene, the activity of the PLAP-2 promoter (but not PLAP-1) was induced with sodium butyrate, while both promoters were induced by 8-Br-cAMP. Inducibility of the PLAP-2 promoter by 8-Br-cAMP was still observed when the promoter was shortened to -103, leaving intact a sequence resembling a cAMP response element. The extent of transcriptional activation by either agent was not sufficient to explain the accumulation of PLAP mRNA. These studies suggest that both transcriptional and posttranscriptional processes are involved in the induction of the PLAP-1 and PLAP-2 gene in JEG-3 cells.
PLAP - 1,它编码胎盘型酶;以及PLAP - 2,它主要在生殖细胞中表达。在绒癌系JEG - 3中,8 - 溴 - 环磷酸腺苷(8 - Br - cAMP)诱导了这两个基因的mRNA积累,而丁酸钠仅诱导了PLAP - 2转录本的积累。通过连续转录分析,每种试剂都提高了一个或两个基因的转录速率。在用与萤火虫荧光素酶基因融合的PLAP启动子转染JEG - 3细胞时,丁酸钠诱导了PLAP - 2启动子(而非PLAP - 1启动子)的活性,而8 - Br - cAMP诱导了两个启动子的活性。当PLAP - 2启动子缩短至 - 103时,仍可观察到8 - Br - cAMP对其的诱导性,此时保留了一个类似cAMP反应元件的序列。两种试剂的转录激活程度均不足以解释PLAP mRNA的积累。这些研究表明,转录和转录后过程均参与了JEG - 3细胞中PLAP - 1和PLAP - 2基因的诱导。