Moffatt B A, Dunn J J, Studier F W
J Mol Biol. 1984 Feb 25;173(2):265-9. doi: 10.1016/0022-2836(84)90194-3.
Differences between two previously published nucleotide sequences for bacteriophage T7 gene 1 have been resolved. The revised sequence has eight changes from the sequence that was used to compile the complete nucleotide sequence of T7 DNA. The revisions do not change the total number of nucleotides in T7 DNA or the predicted number of amino acids in T7 RNA polymerase. Only one of the changes introduces any change in predicted cleavage sites for known restriction endonucleases, and the correctness of the revised sequence at this position has been confirmed by cutting T7 DNA with the appropriate enzyme. However, the revisions do make a substantial difference in the amino acid sequence predicted for T7 RNA polymerase: 37 of the 883 amino acids are changed, 35 because of a shift in reading frame for one stretch of 37 amino acids. The predicted reading frame through this region now agrees with that predicted for the same region of the homologous T3 RNA polymerase. The calculated molecular weight for T7 RNA polymerase is now 98,856.
噬菌体T7基因1两个先前发表的核苷酸序列之间的差异已得到解决。修订后的序列与用于汇编T7 DNA完整核苷酸序列的序列有八个变化。这些修订不会改变T7 DNA中的核苷酸总数或T7 RNA聚合酶中预测的氨基酸数量。只有一个变化会导致已知限制性内切酶预测切割位点的任何变化,并且通过用适当的酶切割T7 DNA已证实了该位置修订序列的正确性。然而,这些修订确实使T7 RNA聚合酶预测的氨基酸序列有了实质性差异:883个氨基酸中有37个发生了变化,其中35个是由于一段37个氨基酸的阅读框发生了移位。现在通过该区域预测的阅读框与同源T3 RNA聚合酶相同区域预测的阅读框一致。T7 RNA聚合酶的计算分子量现在为98,856。