Job C, Dietrich J, Shire D, Teissere M, Job D
Centre National de la Recherche Scientifique, Marseille, France.
Biochem J. 1987 May 15;244(1):151-7. doi: 10.1042/bj2440151.
A kinetic study of the effect of elongating nucleotide concentration on the reactions of abortive elongation catalysed by wheat-germ RNA polymerase II on a poly[d(A-T)] template suggests that the shift from abortive to productive elongation may involve the participation of at least two nucleotides, according to a mechanism very similar to that reported for Escherichia coli RNA polymerase. Experiments performed with non-complementary nucleotides with respect to the DNA template, and with substrate derivatives, allow an analysis of the substrate specificity during these reactions. Similar experiments performed with poly[d(A-A-T)].poly[d(T-T-A)] as template provide a starting point for a better understanding of the effect of DNA sequence on the rates of abortive and productive elongation catalysed by the plant enzyme.
一项关于在聚[d(A-T)]模板上,延伸核苷酸浓度对小麦胚芽RNA聚合酶II催化的流产性延伸反应影响的动力学研究表明,从流产性延伸到持续性延伸的转变可能涉及至少两个核苷酸的参与,其机制与报道的大肠杆菌RNA聚合酶的机制非常相似。用相对于DNA模板非互补的核苷酸以及底物衍生物进行的实验,能够分析这些反应过程中的底物特异性。以聚[d(A-A-T)]·聚[d(T-T-A)]作为模板进行的类似实验,为更好地理解DNA序列对该植物酶催化的流产性延伸和持续性延伸速率的影响提供了一个起点。