Engelke D R
Department of Biological Chemistry, University of Michigan, Ann Arbor 48109.
Gene. 1988;62(2):323-30. doi: 10.1016/0378-1119(88)90569-0.
A cloned repeat of Xenopus laevis satellite I DNA was tested for the ability to form stable complexes with tRNA transcription factors in vitro. In template exclusion studies, the satellite I DNA competed efficiently with a tRNA gene for binding of yeast RNA polymerase III transcription factors. DNase I footprinting further showed that transcription factor TF IIIC alone bound to satellite I DNA at both the A block and B block consensus promoter sequences immediately downstream from the transcription start point. The strength and position of these associations indicate that satellite I DNA is a potential site for association of the same DNA-binding proteins that activate tRNA gene transcription.
对非洲爪蟾卫星I DNA的一个克隆重复片段进行了体外与tRNA转录因子形成稳定复合物能力的测试。在模板排斥研究中,卫星I DNA能有效地与tRNA基因竞争酵母RNA聚合酶III转录因子的结合。DNase I足迹分析进一步表明,单独的转录因子TF IIIC在转录起始点下游紧邻的A框和B框共有启动子序列处与卫星I DNA结合。这些结合的强度和位置表明,卫星I DNA是激活tRNA基因转录的相同DNA结合蛋白的潜在结合位点。