Muiznieks I, Doerfler W
Institute for Genetics, University of Cologne, Weyertal 121, D-50931 Cologne, Germany.
Nucleic Acids Res. 1998 Apr 15;26(8):1899-905. doi: 10.1093/nar/26.8.1899.
DNA restriction fragments, 120-650 base pairs (bp) in length, with 5'-GCGC-3', 5'-GGCC-3' or 3'-GCGC-5' single-stranded overhanging termini, give rise to diffuse bands of unusual electrophoretic mobility in non-denaturing polyacrylamide gels. This shift in electrophoretic mobility can be observed at 4-12 degreesC, not at higher temperatures, but is stabilized by 5-10 mM Mg2+, even at 37 degreesC. The nucleotide sequence in the abutting double-stranded part of the fragment does not affect this phenomenon, which is not caused by dimerization. The altered mobility may be due to the unusual terminal DNA structure, which is dependent on co-operative interactions among more than two neighboring G and C residues. The structure is stabilized by cytidine methylation. The biological role of such fragment structures in DNA repair and recombination is presently unknown.
长度为120 - 650个碱基对(bp)、具有5'-GCGC-3'、5'-GGCC-3'或3'-GCGC-5'单链突出末端的DNA限制性片段,在非变性聚丙烯酰胺凝胶中会产生具有异常电泳迁移率的弥散条带。这种电泳迁移率的变化在4 - 12℃时可以观察到,在更高温度下则观察不到,但即使在37℃时,5 - 10 mM Mg2+也能使其稳定。片段相邻双链部分的核苷酸序列不会影响这一现象,且该现象并非由二聚化引起。迁移率的改变可能归因于异常的末端DNA结构,这种结构依赖于两个以上相邻G和C残基之间的协同相互作用。该结构通过胞嘧啶甲基化得以稳定。目前尚不清楚此类片段结构在DNA修复和重组中的生物学作用。