Bullock P A, Joo W S, Sreekumar K R, Mello C
Department of Biochemistry, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
Virology. 1997 Jan 20;227(2):460-73. doi: 10.1006/viro.1996.8347.
Replication initiation events are suppressed over the SV40 core origin in vitro; they are also greatly reduced over sequences flanking the origin which contain binding sites for several transcription factors. To address the biochemical basis for the gap in initiation events over the flanking sequences, initial synthesis events have been characterized on templates lacking these sequences. Herein, it is demonstrated that previously functional initiation sites are nearly inactive when moved to positions that are proximal to the core origin. Thus, the gap in initiation events depends, in part, on the proximity of the initiation sites to the SV40 core origin. Additional experiments demonstrate that removal of the flanking sequences had little or no effect on DNA unwinding or on the efficiency of initiation of DNA synthesis in vitro. These results indicate that, under our in vitro conditions, initiation of SV40 DNA synthesis is not enhanced by binding of transcription factors to the flanking sequences.
在体外,复制起始事件在SV40核心起始点上受到抑制;在起始点侧翼的序列上,复制起始事件也大幅减少,这些侧翼序列包含多个转录因子的结合位点。为了探究侧翼序列上起始事件存在差异的生化基础,我们对缺乏这些序列的模板上的初始合成事件进行了表征。在此证明,先前具有功能的起始位点移至靠近核心起始点的位置时几乎失去活性。因此,起始事件的差异部分取决于起始位点与SV40核心起始点的距离。额外的实验表明,去除侧翼序列对体外DNA解旋或DNA合成起始效率几乎没有影响。这些结果表明,在我们的体外条件下,转录因子与侧翼序列的结合不会增强SV40 DNA合成的起始。