Gold M, Gefter M, Hausmann R, Hurwitz J
J Gen Physiol. 1966 Jul;49(6):5-28. doi: 10.1085/jgp.49.6.5.
The methylated bases of DNA are formed by the transfer of the methyl group from S-adenosylmethionine to a polynucleotide acceptor. This transfer is catalyzed by highly specific enzymes which recognize a limited number of available sites in the DNA. The mechanism for the recognition is presently unknown. In some instances, there is evidence that other cellular components, such as lipopolysaccharides, can influence the methylation reaction. Certain bacteriophages induce new methylases upon infection of their hosts. Phage T3 is unique in establishing an environment in which methylation of neither the phage nor the host nucleic acid can occur. By superinfecting T3-infected cells with other phages, the latter can be obtained with methyl-deficient DNA. Although a great deal is known about the enzymology of the methylation reaction, and there appears to be a strong correlation between the in vitro and in vivo reactions, studies in which DNA is either supermethylated or totally unmethylated have not yielded any insight as to what the possible function of the methylated bases may be.
DNA 的甲基化碱基是通过甲基基团从 S-腺苷甲硫氨酸转移到多核苷酸受体上形成的。这种转移由高度特异性的酶催化,这些酶识别 DNA 中有限数量的可用位点。目前尚不清楚识别机制。在某些情况下,有证据表明其他细胞成分,如脂多糖,可影响甲基化反应。某些噬菌体在感染宿主时会诱导新的甲基化酶。噬菌体 T3 的独特之处在于建立了一种环境,在这种环境中噬菌体和宿主核酸都不会发生甲基化。通过用其他噬菌体对 T3 感染的细胞进行超感染,可以获得 DNA 甲基化不足的后者。尽管人们对甲基化反应的酶学了解很多,并且体外和体内反应之间似乎有很强的相关性,但对 DNA 进行超甲基化或完全未甲基化的研究尚未对甲基化碱基可能的功能提供任何见解。