T E Wilson

Summary

Affiliation: Washington University School of Medicine
Country: USA

Publications

  1. ncbi request reprint Efficient processing of DNA ends during yeast nonhomologous end joining. Evidence for a DNA polymerase beta (Pol4)-dependent pathway
    T E Wilson
    Department of Pathology, Division of Laboratory Medicine, Washington University School of Medicine, St Louis, Missouri 63110, USA
    J Biol Chem 274:23599-609. 1999
  2. ncbi request reprint Identification of the DNA binding site for NGFI-B by genetic selection in yeast
    T E Wilson
    Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110
    Science 252:1296-300. 1991
  3. ncbi request reprint Yeast DNA ligase IV mediates non-homologous DNA end joining
    T E Wilson
    Washington University School of Medicine, Division of Laboratory Medicine, Department of Pathology, St Louis, Missouri 63110, USA
    Nature 388:495-8. 1997
  4. pmc Repair of DNA strand breaks by the overlapping functions of lesion-specific and non-lesion-specific DNA 3' phosphatases
    J R Vance
    Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109 0602, USA
    Mol Cell Biol 21:7191-8. 2001
  5. ncbi request reprint Uncoupling of 3'-phosphatase and 5'-kinase functions in budding yeast. Characterization of Saccharomyces cerevisiae DNA 3'-phosphatase (TPP1)
    J R Vance
    Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109-0602, USA
    J Biol Chem 276:15073-81. 2001
  6. pmc The orphan receptors NGFI-B and steroidogenic factor 1 establish monomer binding as a third paradigm of nuclear receptor-DNA interaction
    T E Wilson
    Department of Pathology, Washington University School of Medicine, St Louis, Missouri 63110
    Mol Cell Biol 13:5794-804. 1993
  7. ncbi request reprint Activity of DNA ligase IV stimulated by complex formation with XRCC4 protein in mammalian cells
    U Grawunder
    Washington University School of Medicine, Division of Molecular Oncology, Department of Pathology, St Louis, Missouri 63110, USA
    Nature 388:492-5. 1997
  8. ncbi request reprint In vivo mutational analysis of the NGFI-A zinc fingers
    T E Wilson
    Department of Pathology, Washington University School of Medicine, St Louis, Missouri 63110
    J Biol Chem 267:3718-24. 1992

Collaborators

Detail Information

Publications8

  1. ncbi request reprint Efficient processing of DNA ends during yeast nonhomologous end joining. Evidence for a DNA polymerase beta (Pol4)-dependent pathway
    T E Wilson
    Department of Pathology, Division of Laboratory Medicine, Washington University School of Medicine, St Louis, Missouri 63110, USA
    J Biol Chem 274:23599-609. 1999
    ..Pol4 is thus specifically recruited to perform gap-filling in an NHEJ pathway that must also involve as yet unidentified nucleases...
  2. ncbi request reprint Identification of the DNA binding site for NGFI-B by genetic selection in yeast
    T E Wilson
    Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110
    Science 252:1296-300. 1991
    ..Cotransfection experiments in mammalian cells demonstrated that NGFI-B can activate transcription from the NBRE with or without its putative ligand binding domain...
  3. ncbi request reprint Yeast DNA ligase IV mediates non-homologous DNA end joining
    T E Wilson
    Washington University School of Medicine, Division of Laboratory Medicine, Department of Pathology, St Louis, Missouri 63110, USA
    Nature 388:495-8. 1997
    ..Thus, S. cerevisiae has two distinct and separate ligation pathways...
  4. pmc Repair of DNA strand breaks by the overlapping functions of lesion-specific and non-lesion-specific DNA 3' phosphatases
    J R Vance
    Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109 0602, USA
    Mol Cell Biol 21:7191-8. 2001
    ..Taken together, these results demonstrate a clear role for the lesion-specific enzyme, Tpp1, in the repair of a subset of DNA strand breaks...
  5. ncbi request reprint Uncoupling of 3'-phosphatase and 5'-kinase functions in budding yeast. Characterization of Saccharomyces cerevisiae DNA 3'-phosphatase (TPP1)
    J R Vance
    Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109-0602, USA
    J Biol Chem 276:15073-81. 2001
    ..Repair of transformed dephosphorylated plasmids, and 5'-hydroxyl blocking lesions more generally, likely proceeds by a cycle of base removal and resynthesis...
  6. pmc The orphan receptors NGFI-B and steroidogenic factor 1 establish monomer binding as a third paradigm of nuclear receptor-DNA interaction
    T E Wilson
    Department of Pathology, Washington University School of Medicine, St Louis, Missouri 63110
    Mol Cell Biol 13:5794-804. 1993
    ..This monomer-DNA interaction represents a third paradigm of DNA binding by nuclear receptors in addition to direct and inverted dimerization...
  7. ncbi request reprint Activity of DNA ligase IV stimulated by complex formation with XRCC4 protein in mammalian cells
    U Grawunder
    Washington University School of Medicine, Division of Molecular Oncology, Department of Pathology, St Louis, Missouri 63110, USA
    Nature 388:492-5. 1997
    ....
  8. ncbi request reprint In vivo mutational analysis of the NGFI-A zinc fingers
    T E Wilson
    Department of Pathology, Washington University School of Medicine, St Louis, Missouri 63110
    J Biol Chem 267:3718-24. 1992
    ..Surprisingly, not all of the mutations tested significantly impaired NGFI-A-specific DNA binding, suggesting that the function of these zinc fingers is more diverse than previously recognized...