An Efficient DNA Sequencing Strategy Based on the Bacteriophage Mu in Vitro DNA Transposition Reaction

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Figure 1.
Figure 1.

A schematic representation of the utilized in vitro transposition system. (A) cat–Mu minitransposon. The linear transposon fragment is shown to be released from its vector plasmid byBglII digestion; it is therefore in precut configuration. (Rectangles) MuA binding sites; (small arrows) primers used in sequencing. (B) The reaction. MuA forms with the transposon ends a tetrameric transposition complex, a transpososome, that integrates the minitransposon into the target DNA. (ApR, CmR) Ampicillin and chloramphenicol resistance, respectively. (Long arrows) Genes coding for β-lactamase (bla) andCAT (cat); (•) reactive donor DNA 3′ ends.

This Article

  1. Genome Res. 9: 308-315

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