Tomcsanyi T, Berg D E
Department of Microbiology and Immunology, Washington University Medical School, St Louis, MO 63110.
J Mol Biol. 1989 Sep 20;209(2):191-3. doi: 10.1016/0022-2836(89)90271-4.
The two ends of insertion sequence IS50 (from Tn5) differ in sequence and in activity during transposition: the IS50 I end contains DNA adenine methylation (Dam) sites and is affected directly by Dam methylation, whereas the O end lacks Dam sites. The effect of Dam methylation on the transposition of IS50-derived elements with base substitution mutations in their O ends was assayed to understand better how the divergent O and I ends interact. Of 31 O end mutations tested, ten impaired transposition less, and two impaired transposition more in Dam- than in Dam+ cells. These results suggest that the interaction between the two ends in a transposition complex is affected by the sequence or the extent of methylation of one end.
插入序列IS50(来自转座子Tn5)的两端在序列和转座过程中的活性方面存在差异:IS50 I端含有DNA腺嘌呤甲基化(Dam)位点,并直接受Dam甲基化的影响,而O端则缺乏Dam位点。为了更好地理解不同的O端和I端是如何相互作用的,我们检测了Dam甲基化对其O端带有碱基替代突变的IS50衍生元件转座的影响。在测试的31个O端突变中,有10个在Dam -细胞中的转座受损程度小于Dam +细胞,有2个在Dam -细胞中的转座受损程度大于Dam +细胞。这些结果表明,转座复合物中两端之间的相互作用受一端的序列或甲基化程度的影响。