Watt F, Molloy P L
CSIRO Division of Molecular Biology, North Ryde, NSW, Australia.
Nucleic Acids Res. 1988 Feb 25;16(4):1471-86. doi: 10.1093/nar/16.4.1471.
High mobility group proteins 1 and 2 (HMGs 1 and 2) are abundant chromosomal proteins which are believed to be preferentially associated with regions of active chromatin. Our previous results have shown that HMGs 1 and 2 can significantly stimulate specific transcription in vitro from the adenovirus major late promoter. This stimulation is now shown to be due, at least in part, to the influence of HMGs 1 and 2 on binding of a specific transcription factor (MLTF) upstream of the start site of the gene to a region (-66 to -51) which is required for optimal transcription both in vivo and in vitro. HMGs 1 and 2 cause both an increase in the rate of binding of the transcription factor to the DNA and alterations to the pattern of the DNaseI footprint of the factor on the DNA. Different binding states of the factor are also observed dependent on the presence of MgCl2, the factor being bound but not protecting the binding region from DNaseI in the absence of MgCl2.
高迁移率族蛋白1和2(HMGs 1和2)是丰富的染色体蛋白,被认为优先与活性染色质区域相关联。我们之前的结果表明,HMGs 1和2能在体外显著刺激腺病毒主要晚期启动子的特异性转录。现在表明,这种刺激至少部分是由于HMGs 1和2对基因起始位点上游特定转录因子(MLTF)与一个区域(-66至-51)结合的影响,该区域是体内和体外最佳转录所必需的。HMGs 1和2既导致转录因子与DNA结合速率的增加,也导致该因子在DNA上的DNaseI足迹模式的改变。还观察到因子的不同结合状态取决于MgCl2的存在,在没有MgCl2的情况下,因子结合但不保护结合区域免受DNaseI的作用。