Cheng L Z, Workman J L, Kingston R E, Kelly T J
Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Proc Natl Acad Sci U S A. 1992 Jan 15;89(2):589-93. doi: 10.1073/pnas.89.2.589.
Studies of DNA viruses have provided evidence that eukaryotic transcriptional activator proteins can enhance the efficiency of DNA replication as well as transcription. The mechanism of this effect was studied in vitro using the chimeric transcription factor GAL4-VP16 and a DNA template containing GAL4 binding sites adjacent to the simian virus 40 origin of DNA replication. The binding of GAL4-VP16 prevented the repression of DNA replication which otherwise occurred when the template was assembled into chromatin. Relief of repression by GAL4-VP16 required both its DNA-binding and transcriptional activation domains but did not require RNA synthesis. The results are consistent with a general model in which transcriptional activators stimulate eukaryotic DNA replication by modifying the outcome of the competition between initiation factors and histones for occupancy of the origin.
对DNA病毒的研究已提供证据表明,真核转录激活蛋白可提高DNA复制以及转录的效率。利用嵌合转录因子GAL4-VP16和一个含有与猿猴病毒40 DNA复制起点相邻的GAL4结合位点的DNA模板,在体外研究了这种效应的机制。GAL4-VP16的结合阻止了DNA复制的抑制,否则当模板组装成染色质时就会发生这种抑制。GAL4-VP16解除抑制既需要其DNA结合结构域和转录激活结构域,也不需要RNA合成。这些结果与一个普遍模型一致,在该模型中,转录激活因子通过改变起始因子和组蛋白之间竞争占据起点的结果来刺激真核DNA复制。