@article{91141,
  keywords = {Animals, Proteins, Humans, Molecular Sequence Data, Transcription Factors, Restriction Mapping, Amino Acid Sequence, DNA-Binding Proteins, Saccharomyces cerevisiae Proteins, DNA Primers, Polycomb-Group Proteins, DNA, Ribosomal, DNA Helicases, Schizosaccharomyces, Schizosaccharomyces pombe Proteins, DNA, Mitochondrial},
  author = {Jin-Qiu Zhou and Haiyan Qi and Vincent Schulz and Maria Mateyak and Ellen Monson and Virginia Zakian},
  title = {Schizosaccharomyces pombe pfh1+ encodes an essential 5{\textquoteright} to 3{\textquoteright} DNA helicase that is a member of the PIF1 subfamily of DNA helicases.},
  abstract = { The Saccharomyces cerevisiae Pif1p DNA helicase is the prototype member of a helicase subfamily conserved from yeast to humans. S. cerevisiae has two PIF1-like genes, PIF1 itself and RRM3, that have roles in maintenance of telomeric, ribosomal, and mitochondrial DNA. Here we describe the isolation and characterization of pfh1+, a Schizosaccharomyces pombe gene that encodes a Pif1-like protein. Pfh1p was the only S. pombe protein with high identity to Saccharomyces Pif1p. Unlike the two S. cerevisiae Pif1 subfamily proteins, the S. pombe Pfh1p was essential. Like Saccharomyces Pif1p, a truncated form of the S. pombe protein had 5{\textquoteright} to 3{\textquoteright} DNA helicase activity. Point mutations in an invariant lysine residue in the ATP binding pocket of Pfh1p had the same phenotype as deleting pfh1+, demonstrating that the ATPase/helicase activity of Pfh1p was essential. Although mutant spores depleted for Pfh1p proceeded through S phase, they arrested with a terminal cellular phenotype consistent with a postinitiation defect in DNA replication. Telomeric DNA was modestly shortened in the absence of Pfh1p. However, genetic analysis demonstrated that maintenance of telomeric DNA was not the sole essential function of S. pombe Pfh1p. },
  year = {2002},
  journal = {Mol Biol Cell},
  volume = {13},
  pages = {2180-91},
  month = {06/2002},
  issn = {1059-1524},
  language = {eng},
}