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. 2012 Jun;86(11):6222–6230. doi: 10.1128/JVI.00009-12

Fig 1.

Fig 1

Schematic description of the substrates used for assaying the removal of Tf1 SP or PPT substrates. The substrates were prepared as described in detail in Materials and Methods. The 11-nt-long RNA segments with sequences of either the Tf1 SP or PPT were 5′ end labeled with 32P. The labeled RNA was then annealed to Tf1-derived DNA segments with the appropriate 3′ ends that match either the SP sequences (the PBS-derived 40-nt-long DNA) or the PPT (61-nt-long DNA) These heteroduplexes were then elongated with the Klenow fragment of E. coli polymerase I (lacking the 3′→5′ exonuclease), thus producing full-length substrates.