Evidence map›Paper›PMID 1967496›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1990

Molecular dissection of mutations at the heterozygous thymidine kinase locus in mouse lymphoma cells.

M L Applegate, M M Moore, C B Broder, A Burrell, G Juhn, K L Kasweck, P F Lin, A Wadhams, J C Hozier

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
10.2field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 149 citations in OpenAlex.

  1. In Vitro Mouse Lymphoma Cell (L5178Y TkMethods in molecular biology (Clifton, N.J.) · 2026
    Article
  2. Key Challenges forAlternatives to laboratory animals : ATLA · 2024
    Review
  3. Thymidine KinaseFrontiers in toxicology · 2022
    Article
  4. Detection of Loss of Heterozygosity in Tk-Deficient Mutants from L5178Y TkMethods in molecular biology (Clifton, N.J.) · 2020
    Article
  5. Article
  6. Toxicology research · 2014
    Article
  7. Article
  8. Article
  9. Cytotoxicity and mutagenicity of retinol with ultraviolet A irradiation in mouse lymphoma cells.Toxicology in vitro : an international journal published in association with BIBRA · 2010
    Article
  10. Article
  11. Genotoxic effects of acrylamide and glycidamide in mouse lymphoma cells.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2008
    Article
  12. Article
  13. Article
  14. Photomutagenicity of retinyl palmitate by ultraviolet a irradiation in mouse lymphoma cells.Toxicological sciences : an official journal of the Society of Toxicology · 2005
    Article
  15. Review
  16. Article
  17. Carcinogen-induced loss of heterozygosity at the Aprt locus in somatic cells of the mouse.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

M L ApplegateDepartment of Biological Science, Florida State University, Tallahassee 32306.
M M Moore
C B Broder
A Burrell
G Juhn
K L Kasweck
P F Lin
A Wadhams
J C Hozier
Florida State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mouse lymphoma L5178Y TK+/- 3.7.2C cell line allows quantitation of induced TK(+/-)----TK-/- mutations at the heterozygous thymidine kinase (Tk) locus. TK-/- mutant colonies show a bimodal size distribution, reflecting a difference in the growth rates of the two size classes that is hypothesized to result from different degrees of genetic damage. The two homologous chromosomes 11 containing the alleles of the Tk gene in L5178Y 3.7.2C TK+/- cells are distinguishable at the cytogenetic level. We find, in addition, that the two alleles are distinguishable at the molecular level because of an Nco I restriction fragment length polymorphism at the 3' end of the gene. In a set of 51 large-colony and 48 small-colony TK-/- mutants induced by ionizing radiation or by chemical mutagens, we find that 78, including all except one of the small-colony mutants, have lost the Tk+ allele and that some of these have two to four copies of the remaining Tk- allele. Nineteen of the large-colony TK-/- mutants that do not show Tk+ allele loss show no other structural changes detectable at the level of Southern blot analysis. One shows a partial deletion. The variety of mutagenic lesions recorded at the heterozygous Tk locus may be representative of events observed in human malignancy and may include a wider range of mutagenic events than can be observed at hemizygous test loci.

Indexed as

GenesGenetic Carrier ScreeningMutationAllelesAnimalsChromosome MappingDNA, NeoplasmLeukemia, ExperimentalLeukemia L5178MicePolymorphism, Restriction Fragment LengthRestriction MappingThymidine KinaseDNA, NeoplasmThymidine Kinase

Identifiers

PMID1967496
PMCPMC53197
OpenAlexW1995672426

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.