Cited by 201DNA Repair MechanismsDNA and Nucleic Acid ChemistryFungal and yeast genetics research

EXO1-A multi-tasking eukaryotic nuclease

Tran, Phuoc T., Erdeniz, Naz, Symington, Lorraine S., Liskay, R.Michael·2004·DNA Repair

Abstract

Exo1 was first isolated as a 5' --> 3' exonuclease activity induced during meiosis in fission yeast and since that time has been implicated in a multitude of eukaryotic DNA metabolic pathways that include DNA repair, recombination, replication, and telomere integrity. Involvement in multiple pathways affecting genomic stability makes EXO1 a logical target for mutation during oncogenesis. Here, we review studies in several experimental systems that shed light on the role of Exo1 in these DNA transaction pathways, particularly those that may relate to oncogenesis.

Integrity signals

Registry

Crossref · 10.1016/j.dnarep.2004.05.015

Cites

75 of 75 references verified0 citation errors · 0 not checkable

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  • Yeast lacking checkpoint function show no sensitivity to chronic low UV.

    “Experiments performed in yeast cells have suggested that in CLUV conditions no checkpoint is activated, not even during S phase; indeed, checkpoint deficient strains do not exhibit sensitivity to CLUV treatment [62].”

    From Mind the gap: keeping UV lesions in check (2011) · cites this paper as [62]

  • Yeast exposed to chronic low UV show no checkpoint activation, including in S phase.

    “Experiments performed in yeast cells have suggested that in CLUV conditions no checkpoint is activated, not even during S phase; indeed, checkpoint deficient strains do not exhibit sensitivity to CLUV treatment [62].”

    From Mind the gap: keeping UV lesions in check (2011) · cites this paper as [62]

  • Under chronic low UV in yeast, NER is dispensable, as NER-deficient cells also show no sensitivity.

    “Even more surprisingly, NER is not important in these conditions, since NER-deficient cells are also not sensitive to CLUV.”

    From Mind the gap: keeping UV lesions in check (2011) · cites this paper as [62]

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Authors
Tran, P. T., Erdeniz, N., Symington, L. S., & Liskay, R. M.
Affiliations
  • St. Mary's Medical Center (US)
  • Oregon Health & Science University (US)
  • Columbia University (US)
Corresponding author
Liskay, R.Michael
Venue
DNA Repair
Publisher
Elsevier BV
Published
2004-12
Volume
3
Issue
12
Pages
1549-1559
ISSN
  • 1568-7856 (ISSN-L)
  • 1568-7864
OpenAlex
W2019394964
Cited by
201
References
79
Citations by year
2026: 4 · 2025: 5 · 2024: 5 · 2023: 7 · 2022: 2 · 2021: 7 · 2020: 6 · 2019: 9 · 2018: 5 · 2017: 13 · 2016: 10 · 2015: 14 · 2014: 16 · 2013: 14 · 2012: 9
FWCI
0.63
Type
journal article
Language
en
Open access
closed
Locations
  • DNA repair (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health
  • National Institute of General Medical Sciences (GM41784, GM 45413, R01GM045413, R01GM041784)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA and Nucleic Acid Chemistry
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
Keywords
EXO1, exonuclease, DNA recombination, DNA replication, telomere integrity, genome stability, carcinogenesis, meiosis, Schizosaccharomyces pombe, DNA metabolism
MeSH terms
Amino Acid Sequence, Animals, DNA Repair, Exodeoxyribonucleases, Humans, Molecular Sequence Data, Mutation, Neoplasms, Recombination, Genetic, Saccharomyces cerevisiae, Telomere, Protein Structure, Tertiary, DNA Repair Enzymes

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