Evidence map›Paper›PMID 1717994›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1991

Cloning of a human cDNA encoding a CDC2-related kinase by complementation of a budding yeast cdc28 mutation.

J Ninomiya-Tsuji, S Nomoto, H Yasuda, S I Reed, K Matsumoto

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
11.7field-weighted citation impact, top 1% 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

64 citing papers in PubMed, 200 citations in OpenAlex.

  1. Article
  2. Review
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  4. Review
  5. Non-canonical approaches to targeting hypoxic tumors.American journal of cancer research · 2022
    Review
  6. Article
  7. Expression of CDK6 in Oral Squamous Cell CarcinomasAsian Pacific journal of cancer prevention : APJCP · 2018
    Article
  8. Review
  9. Article
  10. Functional cDNA expression cloning: pushing it to the limit.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2012
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
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  20. Article

4 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 2 countries.

J Ninomiya-TsujiDepartment of Molecular Biology, DNAX Research Institute, Palo Alto, CA 94304.
S Nomoto
H Yasuda
S I Reed
K Matsumoto
Palo Alto Institute · USInstitut de Biologie Moléculaire et Cellulaire · FR

Funding

STUDIES ON THE CONTROL OF CELL DIVISION IN YEASTR01GM038328 · NIGMS · SCRIPPS RESEARCH INSTITUTE · PI REED, STEVEN I · 1987 to 1999
–
NIGMS NIH HHS R01GM38328
6 · The paper itself

Abstract

We have cloned two different human cDNAs that can complement cdc28 mutations of budding yeast Saccharomyces cerevisiae. One corresponds to a gene encoding human p34CDC2 kinase, and the other to a gene (CDK2; cell division kinase) that has not been characterized previously. The CDK2 protein is highly homologous to p34CDC2 kinase (65% identical) and more significantly is homologous to Xenopus Eg1 kinase (89% identical), suggesting that CDK2 is the human homolog of Eg1. The human CDC2 and CDK2 genes were both able to complement the inviability of a null allele of S. cerevisiae CDC28. This result indicates that the CDK2 protein has a biological activity closely related to the CDC28 and p34CDC2 kinases. However, CDK2 was unable to complement cdc2 mutants in fission yeast Schizosaccharomyces pombe under the condition where the human CDC2 gene could complement them. CDK2 mRNA appeared late in G1 or in early S phase, slightly before CDC2 mRNA, after growth stimulation in normal human fibroblast cells. These results suggest that in human cells, two different CDC2-like kinases may regulate the cell cycle at distinct stages.

Indexed as

AllelesAmino Acid SequenceAnimalsBase SequenceBlotting, NorthernCDC2 Protein KinaseCell LineCloning, MolecularDNAGenetic Complementation TestHumansKineticsMolecular Sequence DataMutationPlasmidsPoly ACDC2 Protein KinaseDNAPoly ARNARNA, Messenger

Identifiers

PMID1717994
PMCPMC52640
OpenAlexW2067109731

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.