Dynan W S, Tjian R
Cell. 1983 Nov;35(1):79-87. doi: 10.1016/0092-8674(83)90210-6.
Fractionation of HeLa cell extracts reveals the presence of a promoter-specific transcription factor, Sp 1, which activates a class of promoters that includes the SV40 early promoter but not several others that have been tested. We analyzed SV40 early-promoter deletion mutants and determined that transcriptional activation by Sp 1 requires sequences within tandem 21 bp repeats located 70-110 bp upstream of the transcription initiation sites. In a DNAase footprinting assay, Sp 1 protected sequences in this same 21 bp repeat region, thus indicating the presence of a specific site for Sp 1 binding. During purification of Sp 1, there was a correlation between transcription-stimulatory activity and promoter-binding activity. These results suggest that direct binding of Sp 1 to sequences in the upstream promoter element is the mechanism by which this factor activates transcription by RNA polymerase II at the SV40 early promoter.
对HeLa细胞提取物进行分级分离,发现存在一种启动子特异性转录因子Sp1,它能激活一类启动子,包括SV40早期启动子,但不能激活其他几个已测试的启动子。我们分析了SV40早期启动子缺失突变体,确定Sp1的转录激活需要位于转录起始位点上游70 - 110 bp处串联21 bp重复序列内的序列。在DNA酶足迹分析中Sp1保护了同一21 bp重复区域中的序列,因此表明存在Sp1结合的特定位点。在Sp1的纯化过程中,转录刺激活性与启动子结合活性之间存在相关性。这些结果表明,Sp1与上游启动子元件中的序列直接结合是该因子在SV40早期启动子处激活RNA聚合酶II转录的机制。