Butzow J J, Oehrl L L, Eichhorn G L
Laboratory of Cellular and Molecular Biology, National Institute on Aging-Gerontology Research Center, National Institutes of Health, Baltimore, Maryland 21224.
Biochemistry. 1991 Jul 2;30(26):6454-64. doi: 10.1021/bi00240a016.
Escherichia coli RNA polymerase (RNAP) exhibits a strong selectivity for the secondary structure of its template DNA, as shown by the influence both of the DNA conformation on the transcription cycle and of the enzyme on the DNA conformation itself. Binding, chain initiation and elongation characteristics of RNAP, and DNA conformational characteristics were examined by use of the alternating copolymer poly(dGdm5C).poly(dGdm5C) as template. Transcription is impeded when the DNA is in the Z conformation as compared with the B; the initial conformation is determined by the concentration of the conformational effectors of Mg2+ and [Co(NH3)6]3+. RNAP binds to both Z and B conformers; the total binding is moderately greater when the template is in the B conformation than when it is strongly stabilized in the Z, by [Co(NH3)6]3+ concentrations much higher than those required for B-Z transition. However, the Z conformer is much more easily displaced competitively from the bulk of its complexes with RNAP than is the B, indicating a specific binding preference for the B conformer. When the template is in the B conformation, or is moderately stabilized in the Z by Mg2+ concentrations such that the polynucleotide is just fully converted from B to Z, elongation is predicted well by chain initiation, indicating that on the Z conformer RNAP is effectively inhibited at the chain initiation or at an earlier stage. The average chain growth rates for polymeric product synthesized on B and on moderately stabilized Z are similar, even though overall RNA synthesis is considerably lowered on the Z form, again indicating that the limiting events precede elongation. When the Z conformer is strongly stabilized, chain initiation and elongation are further inhibited. Elongation is still roughly correlated with chain initiation, but some additional inhibition of elongation takes place independently. Circular dichroism analysis shows that RNAP-DNA binding affects the B-Z conformational equilibrium, leading to reformation of the B conformer from Z and interference with conversion of B to Z, under conditions that would otherwise favor the Z conformer. Thus, there is an RNAP concentration dependent shift of the B-Z transition to higher concentrations of Z-inducing cation, and there is an RNAP concentration dependent decrease in the rate of B to Z conversion. These effects were observed for poly(dGdm5C).poly(dGdm5C), with Z stabilized by [Co(NH3)6]3+ or Mg2+. (They were observed as well for the unmethylated copolymer poly(dGdC).poly(dGdC), with Z stabilized by [Co(NH3)6]3+.) Perturbation of the Z conformer was detectable by circular dichroism at an RNAP:polynucleotide ratio down to a practical limit of approximately 1 RNAP:500 bp.(ABSTRACT TRUNCATED AT 400 WORDS)
大肠杆菌RNA聚合酶(RNAP)对其模板DNA的二级结构表现出很强的选择性,这已通过DNA构象对转录周期的影响以及酶对DNA构象本身的影响得到证明。使用交替共聚物聚(dGdm5C)·聚(dGdm5C)作为模板,研究了RNAP的结合、链起始和延伸特性以及DNA的构象特征。与B构象相比,当DNA处于Z构象时转录受到阻碍;初始构象由Mg2+和[Co(NH3)6]3+的构象效应物浓度决定。RNAP与Z构象和B构象都结合;当模板处于B构象时,总的结合量比当它被[Co(NH3)6]3+强烈稳定在Z构象时适度大一些,[Co(NH3)6]3+的浓度远高于B-Z转变所需的浓度。然而,Z构象体比B构象体更容易从其与RNAP的大部分复合物中被竞争性取代,这表明对B构象体有特定的结合偏好。当模板处于B构象时,或者通过Mg2+浓度适度稳定在Z构象,使得多核苷酸刚好完全从B转变为Z时,链起始能很好地预测延伸,这表明在Z构象上RNAP在链起始或更早阶段被有效抑制。在B构象和适度稳定的Z构象上合成的聚合物产物的平均链生长速率相似,尽管在Z构象上总的RNA合成显著降低,这再次表明限制事件先于延伸。当Z构象被强烈稳定时,链起始和延伸进一步受到抑制。延伸仍然大致与链起始相关,但延伸会发生一些额外的独立抑制。圆二色性分析表明,RNAP-DNA结合影响B-Z构象平衡,导致在原本有利于Z构象体的条件下,从Z构象体重新形成B构象体,并干扰B向Z的转变。因此,B-Z转变存在RNAP浓度依赖性的向更高浓度的Z诱导阳离子的偏移,并且B向Z转变的速率存在RNAP浓度依赖性的降低。对于聚(dGdm5C)·聚(dGdm5C),用[Co(NH3)6]3+或Mg2+稳定Z构象时观察到了这些效应。(对于未甲基化的共聚物聚(dGdC)·聚(dGdC),用[Co(NH3)6]3+稳定Z构象时也观察到了这些效应。)在RNAP:多核苷酸比例低至约1 RNAP:500 bp的实际极限时,通过圆二色性可检测到Z构象体的扰动。(摘要截断于400字)