Evidence map›Paper›PMID 36897575›Full record

ArticleJournal of cell science2023

Regulation of morphogen pathways by a Drosophila chondroitin sulfate proteoglycan Windpipe.

Woo Seuk Koh, Collin Knudsen, Tomomi Izumikawa, Eriko Nakato, Kristin Grandt, Akiko Kinoshita-Toyoda, Hidenao Toyoda, Hiroshi Nakato

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2023. 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
1.0field-weighted citation impact, top 26% 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, 5 citations in OpenAlex.

  1. Article
  2. Article
  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 2 institutions in 2 countries.

Woo Seuk KohDepartment of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN 55455, USA.
Collin KnudsenDepartment of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN 55455, USA.
Tomomi IzumikawaFaculty of Pharmaceutical Sciences, Ritsumeikan University, Shiga 525-8577, Japan.
Eriko NakatoDepartment of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN 55455, USA.
Kristin GrandtDepartment of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN 55455, USA.
Akiko Kinoshita-ToyodaFaculty of Pharmaceutical Sciences, Ritsumeikan University, Shiga 525-8577, Japan.
Hidenao ToyodaFaculty of Pharmaceutical Sciences, Ritsumeikan University, Shiga 525-8577, Japan.
Hiroshi NakatoDepartment of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN 55455, USA.ORCID 0000-0001-9812-4025
University of Minnesota · USRitsumeikan University · JP

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
DROSOPHILA GENOMICS RESOURCE CENTERP40OD010949 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Andrew Zelhof · 2012 to 2026
$9.4M
Heparan sulfate proteoglycans in signaling and developmentR35GM131688 · NIGMS · UNIVERSITY OF MINNESOTA · PI Hiroshi Nakato · 2019 to 2026
$2.6M
An Interdisciplinary Training Program to Transform Graduate Education In Genetics and GenomicsT32GM140936 · NIGMS · UNIVERSITY OF MINNESOTA · PI ALBERT, FRANK WOLFGANG, GREENSTEIN, DAVID IRWIN · 2021 to 2025
$851k
NIGMS NIH HHS R35 GM131688NIGMS NIH HHS T32 GM140936NIH HHS P40 OD010949NIH HHS P40 OD018537NIH HHS R35 GM131688
6 · The paper itself

Abstract

Morphogens provide quantitative and robust signaling systems to achieve stereotypic patterning and morphogenesis. Heparan sulfate (HS) proteoglycans (HSPGs) are key components of such regulatory feedback networks. In Drosophila, HSPGs serve as co-receptors for a number of morphogens, including Hedgehog (Hh), Wingless (Wg), Decapentaplegic (Dpp) and Unpaired (Upd, or Upd1). Recently, Windpipe (Wdp), a chondroitin sulfate (CS) proteoglycan (CSPG), was found to negatively regulate Upd and Hh signaling. However, the roles of Wdp, and CSPGs in general, in morphogen signaling networks are poorly understood. We found that Wdp is a major CSPG with 4-O-sulfated CS in Drosophila. Overexpression of wdp modulates Dpp and Wg signaling, showing that it is a general regulator of HS-dependent pathways. Although wdp mutant phenotypes are mild in the presence of morphogen signaling buffering systems, this mutant in the absence of Sulf1 or Dally, molecular hubs of the feedback networks, produces high levels of synthetic lethality and various severe morphological phenotypes. Our study indicates a close functional relationship between HS and CS, and identifies the CSPG Wdp as a novel component in morphogen feedback pathways.

Indexed as

DrosophilaDrosophila ProteinsAnimalsChondroitin Sulfate ProteoglycansGene Expression Regulation, DevelopmentalHedgehog ProteinsHeparan Sulfate ProteoglycansMembrane ProteinsSulfatasesWnt1 ProteinChondroitin Sulfate Proteoglycansdpp protein, DrosophilaDrosophila ProteinsHedgehog ProteinsHeparan Sulfate ProteoglycansMembrane ProteinsSULF1 protein, DrosophilaSulfataseswdp protein, DrosophilaWnt1 ProteinChondroitin sulfate proteoglycanDecapentaplegicDrosophilaMorphogen signalingWindpipeWingless

Identifiers

PMID36897575
PMCPMC10113886
OpenAlexW4323812358

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.