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Differential Processing of Leading- and Lagging-Strand Ends at Saccharomyces cerevisiae Telomeres Revealed by the Absence of Rad27p Nuclease
Julie Parenteaua and Raymund J. Wellingeraa Département de Microbiologie et Infectiologie, Faculté de Médecine, Université de Sherbooke, Sherbooke, Quebec J1H 5N4, Canada
Corresponding author: Raymund J. Wellinger, Faculté de Médecine, Université de Sherbooke, 3001 12 Ave. Nord, Sherbooke, Quebec J1H 5N4, Canada., raimund.wellinger{at}usherbrooke.ca (E-mail)
Communicating editor: L. PILLUS
cells. The results from studies of the replication intermediates of a linear plasmid in rad27
cells are consistent with the idea that only one end of the plasmid acquires extensive G-tails, presumably the end made by lagging-strand synthesis. These data further support the notion that chromosome ends have differential requirements for end processing, depending on whether the ends were replicated by leading- or lagging-strand synthesis.
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