Martin C T, Muller D K, Coleman J E
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06510.
Biochemistry. 1988 May 31;27(11):3966-74. doi: 10.1021/bi00411a012.
Immediately following initiation of transcription, T7 RNA polymerase enters a phase in which dissociation of the enzyme-DNA-RNA ternary complex significantly competes with elongation, a process referred to in the Escherichia coli enzyme as abortive cycling [Carpousis, A.J., & Gralla, J.D. (1980) Biochemistry 19, 3245-3253]. Characterization of this process in the T7 RNA polymerase system under various reaction conditions and on templates with differing message sequences reveals that conversion to a highly processive ternary complex occurs after incorporation of eight bases and that the relative competition between dissociation and elongation up to this point is influenced by several different forces. In particular, the sequence dependence of abortive falloff suggests that dissociation is favored immediately following incorporation of UMP and is less likely following incorporation of GMP into the RNA message. Abortive cycling is unchanged in transcription from a synthetic oligonucleotide template which is double-stranded in the promoter region but single-stranded throughout the entire message region. This result proves that melting and reannealing of the DNA duplex in the coding region do not contribute to abortive cycling. Furthermore, weakening of promoter binding by an order of magnitude affects abortive cycling only slightly, suggesting that strong interactions with the promoter are not the major cause of abortive cycling. Kinetic analyses show that conversion to a highly processive ternary complex after the incorporation of eight bases may reflect a large decrease in the unimolecular rate of dissociation of the complex due to increased contacts between the nascent RNA and the DNA template and between RNA and enzyme.(ABSTRACT TRUNCATED AT 250 WORDS)
转录起始后,T7 RNA聚合酶进入一个阶段,在此阶段酶-DNA-RNA三元复合物的解离与延伸存在显著竞争,在大肠杆菌酶中这个过程被称为流产循环[Carpousis, A.J., & Gralla, J.D. (1980) Biochemistry 19, 3245 - 3253]。在各种反应条件下以及不同信息序列的模板上对T7 RNA聚合酶系统中这个过程的表征显示,在掺入八个碱基后会转变为高度持续合成的三元复合物,并且在此之前解离和延伸之间的相对竞争受到几种不同力量的影响。特别是,流产性脱落的序列依赖性表明,UMP掺入后立即有利于解离,而GMP掺入RNA信息后解离的可能性较小。从合成寡核苷酸模板转录时,流产循环没有变化,该模板在启动子区域是双链的,但在整个信息区域是单链的。这一结果证明编码区域DNA双链的解链和重新退火对流产循环没有贡献。此外,启动子结合减弱一个数量级仅对流产循环有轻微影响,这表明与启动子的强相互作用不是流产循环的主要原因。动力学分析表明,掺入八个碱基后转变为高度持续合成的三元复合物可能反映了由于新生RNA与DNA模板以及RNA与酶之间接触增加,复合物单分子解离速率大幅下降。(摘要截断于250字)