Evidence map›Paper›PMID 33367974›Full record

ArticleCell and tissue research2021

Isthmin1, a secreted signaling protein, acts downstream of diverse embryonic patterning centers in development.

Gokul Kesavan, Florian Raible, Mansi Gupta, Anja Machate, Dilara Yilmaz, Michael Brand

Open access · hybridAbstract read
In one paragraph

Article in Cell and tissue research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Advances in research of biological functions of Isthmin-1.Journal of cell communication and signaling · 2023
    Review
  4. Review
  5. Review
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

6 authors at 3 institutions in 3 countries.

Gokul KesavanCenter for Regenerative Therapies TU Dresden (CRTD), Technische Universität Dresden, Fetscherstr 105, 01307, Dresden, Germany. gokul.kesavan@tu-dresden.de.ORCID http://orcid.org/0000-0002-2828-1460
Florian RaibleCenter for Regenerative Therapies TU Dresden (CRTD), Technische Universität Dresden, Fetscherstr 105, 01307, Dresden, Germany.ORCID https://orcid.org/0000-0002-4515-6485
Mansi GuptaCenter for Regenerative Therapies TU Dresden (CRTD), Technische Universität Dresden, Fetscherstr 105, 01307, Dresden, Germany.
Anja MachateCenter for Regenerative Therapies TU Dresden (CRTD), Technische Universität Dresden, Fetscherstr 105, 01307, Dresden, Germany.
Dilara YilmazCenter for Regenerative Therapies TU Dresden (CRTD), Technische Universität Dresden, Fetscherstr 105, 01307, Dresden, Germany.
Michael BrandCenter for Regenerative Therapies TU Dresden (CRTD), Technische Universität Dresden, Fetscherstr 105, 01307, Dresden, Germany. michael.brand@tu-dresden.de.ORCID https://orcid.org/0000-0001-5711-6512
Technische Universität Dresden · DEETH Zurich · CHMax Perutz Labs · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular signals play essential roles during embryonic patterning by providing positional information in a concentration-dependent manner, and many such signals, like Wnt, fibroblast growth factor (FGF), Hedgehog (Hh), and retinoic acid, act by being secreted into the extracellular space, thereby triggering receptor-mediated responses in other cells. Isthmin1 (ism1) is a secreted protein whose gene expression pattern coincides with that of early dorsal determinants, nodal ligand genes like sqt and cyc, and with fgf8 during various phases of zebrafish development. Ism1 functions in early embryonic patterning and development are poorly understood; however, it has recently been shown to interact with nodal pathway genes to control organ asymmetry in chicken. Here, we show that misexpression of ism1 deletion constructs disrupts embryonic patterning in zebrafish and exhibits genetic interactions with both Fgf and nodal signaling. Unlike Fgf and nodal pathway mutants, CRISPR/Cas9-engineered ism1 mutants did not show obvious developmental defects. Further, in vivo single molecule fluorescence correlation spectroscopy (FCCS) showed that Ism1 diffuses freely in the extra-cellular space, with a diffusion coefficient similar to that of Fgf8a; however, our measurements do not support direct molecular interactions between Ism1 and either nodal ligands or Fgf8a in the developing zebrafish embryo. Together, data from gain- and loss-of-function experiments suggest that zebrafish Ism1 plays a complex role in regulating extracellular signals during early embryonic development.

Indexed as

AnimalsAnimals, Genetically ModifiedBody PatterningGene Expression Regulation, DevelopmentalZebrafishZebrafish Proteinsism1 protein, zebrafishZebrafish ProteinsFCSFgf signalingIsthmin1Isthmin2Nodal signalingSecreted factorsZebrafish

Identifiers

PMID33367974
PMCPMC7960586
OpenAlexW3117111269

What OpenQuestion 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 OpenQuestion graph.