Kamzolova S G, Beskaravainy P M, Osypov A A, Dzhelyadin T R, Temlyakova E A, Sorokin A A
a Institute of Cell Biophysics, RAS , 142290 , Pushchino, Moscow region, Russia .
J Biomol Struct Dyn. 2014;32(8):1184-92. doi: 10.1080/07391102.2013.819298. Epub 2013 Jul 30.
The entire T7 bacteriophage genome contains 39937 base pairs (Database NCBI RefSeq N1001604). Here, electrostatic potential distribution around double helical T7 DNA was calculated by Coulomb method using the computer program of Sorokin A.A. (lptolik@gmail.com). Electrostatic profiles of 17 promoters recognized by T7 phage-specific RNA polymerase were analyzed. It was shown that electrostatic profiles of all T7 RNA polymerase-specific promoters can be characterized by distinctive motifs which are specific for each promoter class. Comparative analysis of electrostatic profiles of native T7 promoters of different classes demonstrates that T7 RNA polymerase can differentiate them due to their electrostatic features.
整个T7噬菌体基因组包含39937个碱基对(数据库NCBI RefSeq N1001604)。在此,使用Sorokin A.A.(lptolik@gmail.com)的计算机程序,通过库仑方法计算了双链螺旋T7 DNA周围的静电势分布。分析了T7噬菌体特异性RNA聚合酶识别的17个启动子的静电图谱。结果表明,所有T7 RNA聚合酶特异性启动子的静电图谱都可以由每个启动子类特有的独特基序来表征。对不同类别的天然T7启动子的静电图谱进行比较分析表明,T7 RNA聚合酶可以因其静电特征而区分它们。