Sekiguchi J M, Kmiec E B
Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, Philadelphia, PA 19140.
DNA Cell Biol. 1991 Apr;10(3):223-32. doi: 10.1089/dna.1991.10.223.
We have analyzed transcription factor-mediated DNA supercoiling catalyzed by the Xenopus oocyte extract (S-150). Under conditions that inhibit endogenous supercoiling activity (2 mM EDTA), the 5S RNA specific transcription factor, TFIIIA, promotes a negative change in DNA linking number. The SV40 binding protein, T antigen, appears not to promote DNA supercoiling under these conditions. A nucleosomal ladder can be seen after DNase I digestions only if the DNA template is pre-bound by TFIIIA prior to the addition of the S-150 extract. These studies suggest that TFIIIA may stimulate DNA supercoiling by enhancing the development of protein-DNA interactions via a mechanism that may include nucleosome assembly.
我们分析了非洲爪蟾卵母细胞提取物(S-150)催化的转录因子介导的DNA超螺旋。在抑制内源性超螺旋活性的条件下(2 mM EDTA),5S RNA特异性转录因子TFIIIA可促进DNA连接数的负向变化。在这些条件下,SV40结合蛋白T抗原似乎不会促进DNA超螺旋。只有在加入S-150提取物之前,DNA模板预先与TFIIIA结合,DNase I消化后才能看到核小体梯带。这些研究表明,TFIIIA可能通过增强蛋白质-DNA相互作用的发展来刺激DNA超螺旋,其机制可能包括核小体组装。