Evidence map›Paper›PMID 25756623›Full record

ArticlePloS one2015

Evidence for intermolecular interactions between the intracellular domains of the arabidopsis receptor-like kinase ACR4, its homologs and the Wox5 transcription factor.

Matthew R Meyer, Shweta Shah, J Zhang, Henry Rohrs, A Gururaj Rao

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
6.7field-weighted citation impact, top 4% 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

8 citing papers in PubMed, 27 citations in OpenAlex.

  1. Functional Characterization of the Oat (International journal of molecular sciences · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. PP2A-3 interacts with ACR4 and regulates formative cell division in the Arabidopsis root.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  8. 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

5 authors at 2 institutions in 1 country.

Matthew R MeyerDepartment of Medicine, Washington University School of Medicine, 660 S. Euclid Ave, St. Louis, MO 63130, United States of America.
Shweta ShahRoy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, Iowa 50011, United States of America.
J ZhangNIH NCRR Center for Biomedical and Bio-Organic Mass Spectrometry, Dept. of Chemistry, Washington University, St. Louis, MO 63130, United States of America.
Henry RohrsNIH NCRR Center for Biomedical and Bio-Organic Mass Spectrometry, Dept. of Chemistry, Washington University, St. Louis, MO 63130, United States of America.
A Gururaj RaoRoy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, Iowa 50011, United States of America.
Iowa State University · USWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Arabidopsis CRINKLY4 (ACR4) is a receptor-like kinase (RLK) involved in the global development of the plant. The Arabidopsis genome encodes four homologs of ACR4 that contain sequence similarity and analogous architectural elements to ACR4, termed Arabidopsis CRINKLY4 Related (AtCRRs) proteins. Additionally, a signaling module has been previously proposed including a postulated peptide ligand, CLE40, the ACR4 RLK, and the WOX5 transcription factor that engage in a possible feedback mechanism controlling stem cell differentiation. However, little biochemical evidence is available to ascertain the molecular aspects of receptor heterodimerization and the role of phosphorylation in these interactions. Therefore, we have undertaken an investigation of the in vitro interactions between the intracellular domains (ICD) of ACR4, the CRRs and WOX5. We demonstrate that interaction can occur between ACR4 and all four CRRs in the unphosphorylated state. However, phosphorylation dependency is observed for the interaction between ACR4 and CRR3. Furthermore, sequence analysis of the ACR4 gene family has revealed a conserved 'KDSAF' motif that may be involved in protein-protein interactions among the receptor family. We demonstrate that peptides harboring this conserved motif in CRR3 and CRK1are able to bind to the ACR4 kinase domain. Our investigations also indicate that the ACR4 ICD can interact with and phosphorylate the transcription factor WOX5.

Indexed as

ArabidopsisArabidopsis ProteinsBinding SitesDihydrodipicolinate ReductaseHomeodomain ProteinsMembrane ProteinsModels, MolecularPhosphorylationProtein BindingProtein Serine-Threonine KinasesProtein Structure, SecondaryProtein Structure, TertiaryReceptors, Cell SurfaceACR4 protein, ArabidopsisArabidopsis ProteinsCRR1 protein, ArabidopsisCRR3 protein, ArabidopsisDihydrodipicolinate ReductaseHomeodomain ProteinsMembrane ProteinsProtein Serine-Threonine KinasesReceptors, Cell SurfaceWUSCHEL protein, Arabidopsis

Identifiers

PMID25756623
PMCPMC4355418
OpenAlexW1989536694

What OpenQuestion holds

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Registered trials

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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.