Yang J Q, Remmers E F, Marcu K B
EMBO J. 1986 Dec 20;5(13):3553-62. doi: 10.1002/j.1460-2075.1986.tb04682.x.
We have identified a positive modulator within the c-myc first exon downstream of the gene's transcription initiation sites, P1 and P2. We introduced myc-CAT (chloramphenicol acetyltransferase) hybrid genes into three cell lines (BJAB, COS and HeLa) and measured their expression by either CAT enzymatic activity, S1 nuclease protection or by a nuclear 'run-on' transcription assay. Removal of 46 bp from the 3' end of the first exon results in a decrease of myc-CAT expression and P2 activity. A 438-bp exon 1 segment, lacking the normal myc promoters, efficiently drives the expression of SV40 early promoters. We find that this first exon segment efficiently functions as a positive modulator only in its sense orientation, 3' of a nearby promoter. The positive effects of the myc first exon and the SV40 enhancer are complementary.
我们在c-myc基因转录起始位点P1和P2下游的第一个外显子内鉴定出一种正向调节剂。我们将myc-CAT(氯霉素乙酰转移酶)杂交基因导入三种细胞系(BJAB、COS和HeLa),并通过CAT酶活性、S1核酸酶保护或核“连续”转录测定法测量它们的表达。从第一个外显子的3'末端去除46 bp会导致myc-CAT表达和P2活性降低。一个缺少正常myc启动子的438-bp外显子1片段有效地驱动SV40早期启动子的表达。我们发现,这个第一个外显子片段仅在其正义方向、附近启动子的3'端有效地作为正向调节剂发挥作用。myc第一个外显子和SV40增强子的正向作用是互补的。