Liao W C, Ash J, Johnson L F
Department of Molecular Genetics and Biochemistry, Ohio State University, Columbus 43210.
Nucleic Acids Res. 1994 Oct 11;22(20):4044-9. doi: 10.1093/nar/22.20.4044.
The promoter of the mouse thymidylate synthase (TS) gene lacks both a TATAA box and an initiator element and directs transcriptional initiation at multiple sites over a 90 nucleotide initiation window. Earlier studies defined an essential region near the 5' end of the initiation window that is required for promoter activity. The essential region contains possible binding sites for Sp1 and Ets transcription factors. In the present study we show that this essential region stimulates transcription with approximately equal strength in both directions. Transcription is initiated over a broad initiation window in the reverse direction. The same elements are important for the reverse promoter and for the normal TS promoter. Sequences upstream of the essential region partially suppress expression in the reverse direction. The TS 5' flanking region, in either the normal or inverted orientation, directs S phase-specific expression of a TS minigene. This raises the possibility that an upstream gene and the TS gene may be coordinately induced at the G1/S phase boundary by a common set of control elements.
小鼠胸苷酸合成酶(TS)基因的启动子既缺乏TATAA盒,也没有起始元件,并且在一个90个核苷酸的起始窗口内的多个位点指导转录起始。早期研究确定了起始窗口5'端附近一个对启动子活性至关重要的区域。该关键区域包含Sp1和Ets转录因子的可能结合位点。在本研究中,我们表明这个关键区域在两个方向上以大致相同的强度刺激转录。转录在反向的一个较宽的起始窗口内起始。相同的元件对反向启动子和正常的TS启动子都很重要。关键区域上游的序列部分抑制反向表达。TS 5'侧翼区域,无论是正常方向还是反向方向,都指导TS小基因的S期特异性表达。这增加了一种可能性,即一个上游基因和TS基因可能在G1/S期边界由一组共同的控制元件协同诱导。