4.7 Article

Recruitment of host functions suggests a repair pathway for late steps in group II intron retrohoming

Journal

GENES & DEVELOPMENT
Volume 19, Issue 20, Pages 2477-2487

Publisher

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.1345105

Keywords

retroelement; retrotransposon; RNase H; Pol I; Pol III; repair polymerases

Funding

  1. NIGMS NIH HHS [R01 GM039422, GM37949, R01 GM037949, R37 GM039422, GM39422, R01 GM044844, GM44844] Funding Source: Medline

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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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