Key result
Screening of Escherichia coli mutants revealed strong effects (greater than threefold) for several host repair enzymes on the retrohoming of the Lactococcus lactis Ll.LtrB intron.
The completion of retrohoming is viewed as a DNA repair process involving host enzymes, with features that may be shared by other non-LTR retroelements.
Retrohoming of group II introns occurs by a mechanism in which the intron RNA reverse splices directly into one strand of a DNA target site and is then reverse transcribed by the associated intron-encoded protein. Host repair enzymes are predicted to complete this process. Here, we screened a battery of Escherichia coli mutants defective in host functions that are potentially involved in retrohoming of the Lactococcus lactis Ll.LtrB intron. We found strong (greater than threefold) effects for several enzymes, including nucleases directed against RNA and DNA, replicative and repair polymerases, and DNA ligase. A model including the presumptive roles of these enzymes in resection of DNA, degradation of the intron RNA template, traversion of RNA-DNA junctions, and second-strand DNA synthesis is described. The completion of retrohoming is viewed as a DNA repair process, with features that may be shared by other non-LTR retroelements.
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Smith et al. (2005) studied Retrohoming of group II introns. Escherichia coli mutants defective in host functions was evaluated on Retrohoming of the Lactococcus lactis Ll.LtrB intron. Screening of Escherichia coli mutants revealed strong effects (greater than threefold) for several host repair enzymes on the retrohoming of the Lactococcus lactis Ll.LtrB intron.
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