Diaz G A, Raskin C A, McAllister W T
Morse Institute of Molecular Genetics, Department of Microbiology and Immunology, State University of New York Health Science Center, Brooklyn 11203-2098.
J Mol Biol. 1993 Feb 20;229(4):805-11. doi: 10.1006/jmbi.1993.1086.
The activity of bacteriophage T7 RNA polymerase (RNAP) at a collection of T7 promoter mutants having all possible single base-pair substitutions in the region from -15 to -6 was determined by transcription in vitro, thus establishing a hierarchy of base-pair preference at each position. The tolerance of the RNAP for base-pair substitutions is not uniform across the binding domain. Under stringent conditions (20 mM-MgCl2), T7 RNAP is highly permissive for all base-pair substitutions at -13 and -12. The RNAP is partially permissive at -15, -14, -11, -10 and -6, and exhibits a clear pattern of base-pair preference at these positions. The RNAP is non-permissive for substitutions at -9 to -7, and will accept only the consensus base-pairs at these positions. Under lower stringency conditions (8 mM-MgCl2, or additionally in the presence of dimethylsulfoxide) a decrease in specificity is observed at most positions except -9. Analysis of these data suggests potential contacts that may be important for promoter function.
通过体外转录确定了噬菌体T7 RNA聚合酶(RNAP)在一系列T7启动子突变体上的活性,这些突变体在-15至-6区域具有所有可能的单碱基对替换,从而建立了每个位置碱基对偏好的等级体系。RNAP对碱基对替换的耐受性在结合域中并不均匀。在严格条件下(20 mM - MgCl2),T7 RNAP对-13和-12处的所有碱基对替换具有高度宽容性。RNAP在-15、-14、-11、-10和-6处部分宽容,并在这些位置表现出明显的碱基对偏好模式。RNAP对-9至-7处的替换不宽容,并且在这些位置只接受共有碱基对。在较低严格条件下(8 mM - MgCl2,或另外在二甲基亚砜存在的情况下),除了-9之外,在大多数位置观察到特异性降低。对这些数据的分析表明了可能对启动子功能重要的潜在接触。