Klement J F, Moorefield M B, Jorgensen E, Brown J E, Risman S, McAllister W T
Department of Microbiology and Immunology, Morse Institute of Molecular Genetics, SUNY-Health Science Center, Brooklyn 11203-2098.
J Mol Biol. 1990 Sep 5;215(1):21-9. doi: 10.1016/s0022-2836(05)80091-9.
The bacteriophage T3 and T7 RNA polymerases are closely related, yet are highly specific for their own promoter sequences. To understand the basis of this specificity, T7 promoter variant that contain substitutions of T3-specific base-pairs at one or more positions within the T7 promoter consensus sequence were synthesized and cloned. Template competition assays between variant and consensus promoters demonstrate that the primary determinants of promoter specificity are located in the region from -10 to -12, and that the base-pair at -11 is of particular importance. Changing this base-pair from G.C, which is normally present in T7 promoters, to C.G, which is found at this position in T3 promoters, prevented utilization by the T7 RNA polymerase and simultaneously enabled transcription from the variant T7 promoter by the T3 enzyme. Substitution of T7 base-pairs with T3 base-pairs at other positions where the two consensus sequences diverge affected the overall efficiency with which the variant promoter was utilized by the T7 RNA polymerase, but these changes were not sufficient to permit recognition by the T3 RNA polymerase. Switching the -11 base-pair in the T3 promoter consensus to the T7 base-pair prevented utilization by the T3 RNA polymerase, but did not allow the T3 variant promoter to be utilized by the T7 RNA polymerase. This probably reflects a greater specificity of the T7 RNA polymerase for base-pairs at other positions where the promoter sequences differ, most notably at -15. The magnitude of the effects of base substitutions in the T7 promoter on promoter strength (-11C much greater than -10C greater than -12A) correlates with the affinity of the T7 polymerase for the promoter variants, suggesting that the discrimination of the phage RNA polymerases for their promoters is mediated primarily at the level of DNA binding, rather than at the level of initiation.
噬菌体T3和T7 RNA聚合酶密切相关,但对其自身的启动子序列具有高度特异性。为了理解这种特异性的基础,合成并克隆了T7启动子变体,这些变体在T7启动子共有序列内的一个或多个位置含有T3特异性碱基对的替换。变体启动子和共有启动子之间的模板竞争试验表明,启动子特异性的主要决定因素位于-10至-12区域,并且-11处的碱基对尤为重要。将该碱基对从T7启动子中通常存在的G.C改变为T3启动子中该位置发现的C.G,阻止了T7 RNA聚合酶的利用,同时使T3酶能够从变体T7启动子进行转录。在两个共有序列不同的其他位置用T3碱基对替换T7碱基对影响了T7 RNA聚合酶利用变体启动子的总体效率,但这些变化不足以允许T3 RNA聚合酶识别。将T3启动子共有序列中的-11碱基对切换为T7碱基对阻止了T3 RNA聚合酶的利用,但不允许T7 RNA聚合酶利用T3变体启动子。这可能反映了T7 RNA聚合酶对启动子序列不同的其他位置的碱基对具有更高的特异性,最显著的是在-15处。T7启动子中碱基替换对启动子强度的影响程度(-11C远大于-10C大于-12A)与T7聚合酶对启动子变体的亲和力相关,这表明噬菌体RNA聚合酶对其启动子的识别主要在DNA结合水平介导,而不是在起始水平。