Evidence map›Paper›PMID 8811088›Full record

ArticleNucleic acids research1996

The reverse two-hybrid system: a genetic scheme for selection against specific protein/protein interactions.

C A Leanna, M Hannink

Open access · bronzeAbstract read
In one paragraph

Article in Nucleic acids research, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. International journal of molecular sciences · 2019
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. A systematic method for identifying small-molecule modulators of protein-protein interactions.Proceedings of the National Academy of Sciences of the United States of America · 2004
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Yeast Two-Hybrid: State of the Art.Biological procedures online · 1999
    Article
  19. An artificial cell-cycle inhibitor isolated from a combinatorial library.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
  20. A yeast genetic system for selecting small molecule inhibitors of protein-protein interactions in nanodroplets.Proceedings of the National Academy of Sciences of the United States of America · 1997
    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

2 authors at 1 institution in 1 country.

C A LeannaBiochemistry Department, University of Missouri-Columbia 65212, USA.
M Hannink
University of Missouri · US

Funding

ONCOGENIC INTERACTIONS BETWEEN V-REL AND NF-KB PROTEINSR29CA055027 · NCI · UNIVERSITY OF MISSOURI-COLUMBIA · PI HANNINK, MARK · 1992 to 1995
–
NCI NIH HHS CA-55027
6 · The paper itself

Abstract

The yeast two-hybrid system is a powerful experimental approach for the characterization of protein/ protein interactions. A unique strength of the yeast two-hybrid system is the provision for genetic selection techniques that enable the identification of specific protein/protein interactions. We now report the development of a modified yeast two-hybrid system which enables genetic selection against a specific protein/protein interaction. This reverse two-hybrid system utilizes a yeast strain which is resistant to cycloheximide due to the presence of a mutant cyh2 gene. This strain also contains the wild-type CYH2 allele under the transcriptional control of the Gal1 promoter. Expression of the wild-type Gal4 protein is sufficient to restore growth sensitivity to cycloheximide. Growth sensitivity towards cycloheximide is also restored by the coexpression of the avian c-Rel protein and its I kappa B alpha counterpart, p40, as Gal4 fusion proteins. Restoration of growth sensitivity towards cycloheximide requires the association of c-Rel and p40 at the Gal1 promoter and correlates with the ability of the c-Rel/p40 interaction to activate expression from the Gal1 promoter. A genetic selection scheme against specific protein/protein interactions may be a valuable tool for the analysis of protein/protein interactions.

Indexed as

I-kappa B ProteinsSaccharomyces cerevisiae ProteinsTranscription FactorsAnkyrinsCloning, MolecularCycloheximideDNA-Binding ProteinsDrug Resistance, MicrobialFungal ProteinsGenes, ReporterMutagenesisNF-KappaB Inhibitor alphaPromoter Regions, GeneticProtein BindingProto-Oncogene ProteinsProto-Oncogene Proteins c-relAnkyrinsCycloheximideDNA-Binding ProteinsFungal ProteinsGAL4 protein, S cerevisiaeI-kappa B ProteinsNF-KappaB Inhibitor alphaProto-Oncogene ProteinsProto-Oncogene Proteins c-relSaccharomyces cerevisiae ProteinsTranscription Factors

Identifiers

PMID8811088
PMCPMC146093
OpenAlexW2067476911

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.