Bélanger C, Peri K G, MacKenzie R E
Department of Biochemistry, McGill University, Montréal, Québec, Canada.
Nucleic Acids Res. 1991 Aug 25;19(16):4341-5. doi: 10.1093/nar/19.16.4341.
Sequence analysis of the 5'-flanking region of the gene encoding NAD-dependent methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase (NMDMC) revealed several putative cis-regulatory elements. To delineate the function of these regulatory elements, various deletion mutants of the 5'-flanking region were connected to the reporter gene chloramphenicol acetyltransferase (CAT) and promoter activity was measured in transient transfection assays. Transfection experiments performed with the sequence extending from -508 to +59 produced a high-level transient expression of the CAT gene in BALB/c 3T3-SV-T2 and NIH 3T3 cells. Removal of the sequence from +16 to +59 which includes the second transcription start point at +43, a TATA-like box and 5'-untranslated sequences abolished the promoter activity. Deletion analysis of 5'-upstream sequences revealed that the region from positions -55 to +59 is sufficient to mediate a high CAT activity comparable to the level obtained with the construct -508/+59. Within this region are found a CAAT box, a TATA-like box and two putative GC boxes. A functional analysis of the promoter showed that the sequence from -55 to +59 is sufficient to respond to stimulation by serum.
对编码NAD依赖性亚甲基四氢叶酸脱氢酶-亚甲基四氢叶酸环水解酶(NMDMC)的基因5'-侧翼区域进行序列分析,发现了几个假定的顺式调控元件。为了阐明这些调控元件的功能,将5'-侧翼区域的各种缺失突变体与报告基因氯霉素乙酰转移酶(CAT)相连,并在瞬时转染试验中测量启动子活性。用从-508到+59的序列进行的转染实验在BALB/c 3T3-SV-T2和NIH 3T3细胞中产生了高水平的CAT基因瞬时表达。去除从+16到+59的序列,该序列包括位于+43的第二个转录起始点、一个类TATA盒和5'-非翻译序列,启动子活性消失。对5'-上游序列的缺失分析表明,从-55到+59的区域足以介导与构建体-508/+59获得的水平相当的高CAT活性。在该区域内发现一个CAAT盒、一个类TATA盒和两个假定的GC盒。对启动子的功能分析表明,从-55到+59的序列足以响应血清刺激。