Evidence map›Paper›PMID 32198667›Full record

ArticleDevelopment genes and evolution2020

What lies beneath: Hydra provides cnidarian perspectives into the evolution of FGFR docking proteins.

Ashwini Suryawanshi, Karolin Schaefer, Oliver Holz, David Apel, Ellen Lange, David C Hayward, David J Miller, Monika Hassel

Open access · hybridAbstract read
In one paragraph

Article in Development genes and evolution, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

8 authors at 3 institutions in 2 countries.

Ashwini SuryawanshiMorphology and Evolution of Invertebrates, Philipps University, FB17, Karl von Frisch Str. 8, 35032, Marburg, Germany.
Karolin SchaeferMorphology and Evolution of Invertebrates, Philipps University, FB17, Karl von Frisch Str. 8, 35032, Marburg, Germany.
Oliver HolzMorphology and Evolution of Invertebrates, Philipps University, FB17, Karl von Frisch Str. 8, 35032, Marburg, Germany.
David ApelMorphology and Evolution of Invertebrates, Philipps University, FB17, Karl von Frisch Str. 8, 35032, Marburg, Germany.
Ellen LangeMorphology and Evolution of Invertebrates, Philipps University, FB17, Karl von Frisch Str. 8, 35032, Marburg, Germany.
David C HaywardResearch School of Biology, Australian National University, Canberra, ACT, 0200, Australia.
David J MillerARC Centre of Excellence for Coral Reef Studies, James Cook University, Townsville, Queensland, 4811, Australia.
Monika HasselMorphology and Evolution of Invertebrates, Philipps University, FB17, Karl von Frisch Str. 8, 35032, Marburg, Germany. hassel@staff.uni-marburg.de.
Philipps University of Marburg · DEARC Centre of Excellence for Coral Reef Studies · AUAustralian National University · AU

Funding

Deutsche Forschungsgemeinschaft HA1732/13
6 · The paper itself

Abstract

Across the Bilateria, FGF/FGFR signaling is critical for normal development, and in both Drosophila and vertebrates, docking proteins are required to connect activated FGFRs with downstream pathways. While vertebrates use Frs2 to dock FGFR to the RAS/MAPK or PI3K pathways, the unrelated protein, downstream of FGFR (Dof/stumps/heartbroken), fulfills the corresponding function in Drosophila. To better understand the evolution of the signaling pathway downstream of FGFR, the available sequence databases were screened to identify Frs2, Dof, and other key pathway components in phyla that diverged early in animal evolution. While Frs2 homologues were detected only in members of the Bilateria, canonical Dof sequences (containing Dof, ankyrin, and SH2/SH3 domains) were present in cnidarians as well as bilaterians (but not in other animals or holozoans), correlating with the appearance of FGFR. Although these data suggested that Dof coupling might be ancestral, gene expression analysis in the cnidarian Hydra revealed that Dof is not upregulated in the zone of strong FGFRa and FGFRb expression at the bud base, where FGFR signaling controls detachment. In contrast, transcripts encoding other, known elements of FGFR signaling in Bilateria, namely the FGFR adaptors Grb2 and Crkl, which are acting downstream of Dof (and Frs2), as well as the guanyl nucleotide exchange factor Sos, and the tyrosine phosphatase Csw/Shp2, were strongly upregulated at the bud base. Our expression analysis, thus, identified transcriptional upregulation of known elements of FGFR signaling at the Hydra bud base indicating a highly conserved toolkit. Lack of transcriptional Dof upregulation raises the interesting question, whether Hydra FGFR signaling requires either of the docking proteins known from Bilateria.

Indexed as

Biological EvolutionAdaptor Proteins, Signal TransducingAnimalsCnidariaGene Expression Regulation, DevelopmentalGRB2 Adaptor ProteinHydraPhylogenyProtein Tyrosine Phosphatase, Non-Receptor Type 11Receptors, Fibroblast Growth FactorSignal TransductionSon of Sevenless ProteinsAdaptor Proteins, Signal TransducingCRKL proteinGRB2 Adaptor ProteinProtein Tyrosine Phosphatase, Non-Receptor Type 11Receptors, Fibroblast Growth FactorSon of Sevenless ProteinsAdapter proteinCrklDofGrb2Receptor tyrosine kinase

Identifiers

PMID32198667
PMCPMC7260276
OpenAlexW3010668083

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.