Lopez P, Espinosa M, Piechowska M, Shugar D, Warren R A
J Virol. 1981 Feb;37(2):559-63. doi: 10.1128/JVI.37.2.559-563.1981.
The DNA of bacteriophage phi W-14 is unusual in that half of the thymine residues are replaced with the hypermodified pyrimidine alpha-putrescinylthymine (Kropinski et al., Biochemistry 12:151-157, 1973). Bacteriophage phi W-14 DNA and Bacillus subtilis DNA exhibited comparable competing abilities for the uptake of transfecting bacteriophage SPP1 DNA by competent cells of B. subtilis. B. subtilis DNA decreased transfection and uptake to the same extent, indicating that it merely competed with SPP1 DNA for uptake. Phi W-14 DNA, however, decreased transfection up to 30 times more effectively than it inhibited uptake. Phi W-14 DNA did not alter the kinetics of transfection. The degree of inhibition of transfection was dependent upon the time of addition of Phi W-14 DNA relative to the time of addition of SPP1 DNA. If failed to inhibit when added 30 min after SPP1 DNA. It had a fourfold-greater effect when added 10 min before, rather than simultaneously with, SPP1, but this enhancement was abolished by high concentrations of SPP1 DNA. The nature of the transfection process was not altered in those cells escaping inhibition by Phi W-14 DNA: two molecules of transfecting SPP1 DNA were required to form a transfectant with or without Phi W-14 DNA. Free putrescine did not affect transfection by SPP1 DNA. It was concluded that the putrescine groups covalently attached to phi W-14 DNA allowed this DNA to interfere with the transfection process at the intracellular level.
噬菌体φW - 14的DNA不同寻常之处在于,其一半的胸腺嘧啶残基被超修饰的嘧啶α-腐胺基胸腺嘧啶所取代(克罗平斯基等人,《生物化学》12:151 - 157,1973)。噬菌体φW - 14 DNA和枯草芽孢杆菌DNA在枯草芽孢杆菌感受态细胞摄取转染噬菌体SPP1 DNA方面表现出相当的竞争能力。枯草芽孢杆菌DNA在相同程度上降低了转染和摄取,表明它只是与SPP1 DNA竞争摄取。然而,φW - 14 DNA降低转染的效果比抑制摄取的效果高30倍。φW - 14 DNA没有改变转染动力学。转染抑制程度取决于相对于添加SPP1 DNA的时间添加φW - 14 DNA的时间。如果在SPP1 DNA添加30分钟后添加,它无法抑制。在SPP1之前10分钟添加而非同时添加时,其效果增强四倍,但这种增强被高浓度的SPP1 DNA消除。在那些逃脱φW - 14 DNA抑制的细胞中,转染过程的性质没有改变:无论有无φW - 14 DNA,形成一个转染体都需要两个转染SPP1 DNA分子参与。游离腐胺不影响SPP1 DNA的转染。得出的结论是,共价连接到φW - 14 DNA上的腐胺基团使该DNA能够在细胞内水平干扰转染过程。