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. 2001 Jun 15;20(12):3229–3237. doi: 10.1093/emboj/20.12.3229

graphic file with name cde290f5.jpg

Fig. 5. Test for hairpin telomere at the left end in the resolved substrate. (A) The schematic shows the telomeric structure of wild-type lp17 and the position of an EcoNI site located 2639 bp from the left end. The right panel shows a Southern blot of a 1% agarose gel containing EcoNI-digested B.burgdorferi plasmid DNA hybridized with Probe 1. Duplicate samples were loaded without (–) or with (+) heat treatment at 95°C for 6 min, followed by incubation at 0°C, as indicated. (B) The schematic shows the position of an XhoI site 2538 bp from the left end of the resolved telomere substrate. The blot on the right contains XhoI-digested plasmid DNA from a B.burgdorferi transformant carrying the resolved telomere substrate. The blot was hybridized with Probe 2 (kan). (C) The schematic shows the resolved telomere substrate cut with both XhoI and BamHI to remove the hairpin end on a 70 bp fragment. The blot on the right was also hybridized with Probe 2.