Habib G M, Carter B Z, Sepulveda A R, Shi Z Z, Wan D F, Lebovitz R M, Lieberman M W
Department of Pathology, Baylor College of Medicine, Houston, Texas 77030, USA.
J Biol Chem. 1995 Jun 9;270(23):13711-5. doi: 10.1074/jbc.270.23.13711.
We have previously identified five promoters in the 5'-flanking region of the mouse gamma-glutamyl transpeptidase (gamma GT) gene. We now report the localization of a sixth promoter that supports the transcription of type III RNA, the major gamma GT RNA in fetal liver. We made a fetal liver cDNA library enriched for gamma GT RNA and obtained 12 gamma GT type III-specific clones. The longest clone is consistent with a transcription start site for type III RNA at a position 5' to the type IV promoter and about 5 kilobase(s) (kb) 5' to the first coding exon. We estimated by ribonuclease protection assay that about 80% of the gamma GT mRNA in fetal liver was type III. Primer extension and nuclease protection analyses mapped the 5' end of type III mRNA in fetal liver and kidney to a single cluster of potential major and minor transcription start sites. Deletion analysis using transient expression of chloramphenicol acetyltransferase constructs of the type III promoter region revealed the greatest activity with a 1-kb 5'-flanking fragment in mouse kidney proximal tubular cells and no detectable activity in NIH-3T3 fibroblasts. These studies demonstrate that the type III 5' region of the mouse gamma GT gene is organized into two distinct exons (IIIa and IIIb) and that type III RNA is expressed under the control of its own promoter.
我们之前已在小鼠γ-谷氨酰转肽酶(γGT)基因的5'侧翼区域鉴定出5个启动子。我们现在报告第六个启动子的定位,该启动子支持III型RNA的转录,III型RNA是胎儿肝脏中主要的γGT RNA。我们构建了一个富含γGT RNA的胎儿肝脏cDNA文库,并获得了12个γGT III型特异性克隆。最长的克隆与III型RNA的转录起始位点一致,该位点位于IV型启动子的5'端,且在第一个编码外显子的5'端约5千碱基(kb)处。我们通过核糖核酸酶保护试验估计,胎儿肝脏中约80%的γGT mRNA是III型。引物延伸和核酸酶保护分析将胎儿肝脏和肾脏中III型mRNA的5'端定位到单个潜在的主要和次要转录起始位点簇。使用III型启动子区域的氯霉素乙酰转移酶构建体进行瞬时表达的缺失分析表明,在小鼠肾近端小管细胞中,1-kb的5'侧翼片段具有最大活性,而在NIH-3T3成纤维细胞中未检测到活性。这些研究表明,小鼠γGT基因的III型5'区域被组织成两个不同的外显子(IIIa和IIIb),且III型RNA在其自身启动子的控制下表达。