Stünkel W, Kober I, Kauer M, Taimor G, Seifart K H
Institut für Molekularbiologie und Tumorforschung, Phillips Universität Marburg, Germany.
Nucleic Acids Res. 1995 Jan 11;23(1):109-16. doi: 10.1093/nar/23.1.109.
Plasmid DNA harbouring the human 5S rRNA gene was assembled into nucleosomes using either Xenopus S150 extracts or purified core histones in the presence of pectin. In both cases reconstitution of nucleosomes led to a complete repression of transcription. This repression could be efficiently counteracted by preincubating the template DNA with highly purified hTFIIIA which allowed the protein to bind to the ICR of the 5S gene. By using an efficient and well-defined in vitro reconstitution system based on isolated core histones in the presence of pectin, which is devoid of endogenous transcription factors, we demonstrate here for the first time that human TFIIIA alone is sufficient to prevent nucleosomal repression of h5S gene transcription and that additional pol III transcription factors are not required to achieve this effect. Additionally, we investigated the binding of hTFIIIA to a mononucleosome reconstituted on the human 5S gene. DNAse I footprinting experiments reveal that the entire ICR of the human 5S gene is covered by the nucleosome, thereby precluding the subsequent binding of human TFIIIA to the promoter of the 5S gene.
携带人类5S rRNA基因的质粒DNA在果胶存在的情况下,使用非洲爪蟾S150提取物或纯化的核心组蛋白组装成核小体。在这两种情况下,核小体的重建都导致转录完全抑制。通过将模板DNA与高度纯化的hTFIIIA预孵育,可以有效地抵消这种抑制作用,hTFIIIA能使该蛋白结合到5S基因的ICR上。通过使用一种高效且明确的体外重建系统,该系统基于在果胶存在下分离的核心组蛋白,且不含内源性转录因子,我们首次证明单独的人类TFIIIA足以防止核小体对h5S基因转录的抑制,并且实现这种效果不需要额外的pol III转录因子。此外,我们研究了hTFIIIA与在人类5S基因上重建的单核小体的结合。DNA酶I足迹实验表明,人类5S基因的整个ICR被核小体覆盖,从而排除了人类TFIIIA随后与5S基因启动子的结合。