Cited by 370DNA Repair MechanismsFungal and yeast genetics researchBacterial Genetics and Biotechnology

The DOI matches its Crossref record; 54 of the 58 references it cites were found in a registry or an index.

TEL1, an S. cerevisiae homolog of the human gene mutated in ataxia telangiectasia, is functionally related to the yeast checkpoint gene, MEC1

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Abstract

Patients with the genetic disorder ataxia telangiectasia (AT) have mutations in the AT mutated (ATM) gene, which is homologous to TEL1 and the checkpoint gene MEC1. A tel1 deletion mutant, unlike a mec1 deletion, is viable and does not exhibit increased sensitivity to DNA-damaging agents. However, increased dosage of TEL1 rescues sensitivity of a mec1 mutant, mec1-1, to DNA-damaging agents and rescues viability of a mec1 disruption. mec1-1 tel1 delta 1 double mutants are synergistically sensitive to DNA-damaging agents, including radiomimetic drugs. These data indicate that TEL1 and MEC1 are functionally related and that functions of the ATM gene are apparently divided between at least two S. cerevisiae homologs.

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Crossref · 10.1016/0092-8674(95)90480-8

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Metadata

Authors
Morrow, D. M., Tagle, D. A., Shiloh, Y., Collins, F. S., & Hieter, P.
Affiliations
  • Johns Hopkins University (US)
  • National Institutes of Health (US)
  • Tel Aviv University (IL)
Venue
Cell
Publisher
Elsevier BV
Published
1995-09
Volume
82
Issue
5
Pages
831-840
ISSN
0092-8674 (ISSN-L)
OpenAlex
W2028263332
Cited by
370
References
58
Citations by year
2026: 1 · 2025: 2 · 2024: 3 · 2023: 2 · 2022: 3 · 2021: 1 · 2020: 7 · 2019: 5 · 2018: 4 · 2017: 5 · 2016: 9 · 2015: 8 · 2014: 6 · 2013: 8 · 2012: 7
FWCI
14.99
Type
journal article
Language
en
Open access
Locations
  • Cell (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
Funders
  • U.S. Department of Energy
  • National Institute for Health and Care Research
  • Ministerio de Economía y Competitividad
  • National Institutes of Health
  • National Cancer Institute (CA-16519, P01CA016519)
  • National Institute of General Medical Sciences (GM162283)
  • National Institute of Neurological Disorders and Stroke (R01NS031763, NS 31763)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
Keywords
Tel1, Mec1, ataxia telangiectasia, ATM gene, DNA damage checkpoint, radiomimetic drugs, dosage compensation, Saccharomyces cerevisiae
MeSH terms
Ataxia Telangiectasia, Base Sequence, Bleomycin, Cloning, Molecular, DNA Damage, Fungal Proteins, Gamma Rays, Genes, Fungal, Humans, Hydroxyurea, Molecular Sequence Data, Mutation, Phenotype, Saccharomyces cerevisiae, Streptonigrin, Ultraviolet Rays, Protein Serine-Threonine Kinases, Sequence Homology, Amino Acid, Saccharomyces cerevisiae Proteins, Intracellular Signaling Peptides and Proteins

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