Evidence map›Paper›PMID 33309948›Full record

ArticleDevelopmental biology2021

Multi-tissue patterning drives anterior morphogenesis of the C. elegans embryo.

Stéphanie Grimbert, Karina Mastronardi, Victoria Richard, Ryan Christensen, Christopher Law, Khashayar Zardoui, David Fay, Alisa Piekny

Open access · hybridAbstract read
In one paragraph

Article in Developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Pathways that affect anterior morphogenesis inbioRxiv : the preprint server for biology · 2023
    Article
  3. Article
  4. Journal of developmental biology · 2020
    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

8 authors at 3 institutions in 2 countries.

Stéphanie GrimbertDepartment of Biology, Concordia University, 7141 Sherbrooke Street West, Montreal, Quebec, H4B 1R6, Canada.
Karina MastronardiDepartment of Biology, Concordia University, 7141 Sherbrooke Street West, Montreal, Quebec, H4B 1R6, Canada.
Victoria RichardDepartment of Biology, Concordia University, 7141 Sherbrooke Street West, Montreal, Quebec, H4B 1R6, Canada.
Ryan ChristensenLaboratory of High Resolution Optical Imaging, NIH/NIBIB, 13 South Drive, Bethesda, MD, 20892, USA.
Christopher LawDepartment of Biology, Concordia University, 7141 Sherbrooke Street West, Montreal, Quebec, H4B 1R6, Canada.
Khashayar ZardouiDepartment of Biology, Concordia University, 7141 Sherbrooke Street West, Montreal, Quebec, H4B 1R6, Canada.
David FayDepartment of Molecular Biology, University of Wyoming, 1000 E. University Ave., Laramie, WY, 82071, USA.
Alisa PieknyDepartment of Biology, Concordia University, 7141 Sherbrooke Street West, Montreal, Quebec, H4B 1R6, Canada. Electronic address: alisa.piekny@concordia.ca.
Concordia University · CANational Institute of Biomedical Imaging and Bioengineering · USUniversity of Wyoming · US

Funding

Wyoming INBRE Phase 4- Equipment Supplement for x-ray diffractometer for Center for Advanced Scientific InstrumentationP20GM103432 · NIGMS · UNIVERSITY OF WYOMING · PI Nicolas A. Blouin · 2012 to 2026
$56.8M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
In vivo regulation of the extracellular matrixR35GM136236 · NIGMS · UNIVERSITY OF WYOMING · PI David S Fay · 2020 to 2026
$3.8M
Mechanisms controlling tissue morphogenesis, architecture, and the response to mechanical forces in C. elegans.R01GM125091 · NIGMS · UNIVERSITY OF WYOMING · PI FAY, DAVID S · 2017 to 2019
$776k
NIGMS NIH HHS P20 GM103432NIGMS NIH HHS R01 GM125091NIGMS NIH HHS R35 GM136236NIH HHS P40 OD010440
6 · The paper itself

Abstract

Complex structures derived from multiple tissue types are challenging to study in vivo, and our knowledge of how cells from different tissues are coordinated is limited. Model organisms have proven invaluable for improving our understanding of how chemical and mechanical cues between cells from two different tissues can govern specific morphogenetic events. Here we used Caenorhabditis elegans as a model system to show how cells from three different tissues are coordinated to give rise to the anterior lumen. While some aspects of pharyngeal morphogenesis have been well-described, it is less clear how cells from the pharynx, epidermis and neuroblasts coordinate to define the location of the anterior lumen and supporting structures. Using various microscopy and software approaches, we define the movements and patterns of these cells during anterior morphogenesis. Projections from the anterior-most pharyngeal cells (arcade cells) provide the first visible markers for the location of the future lumen, and facilitate patterning of the surrounding neuroblasts. These neuroblast patterns control the rate of migration of the anterior epidermal cells, whereas the epidermal cells ultimately reinforce and control the position of the future lumen, as they must join with the pharyngeal cells for their epithelialization. Our studies are the first to characterize anterior morphogenesis in C. elegans in detail and should lay the framework for identifying how these different patterns are controlled at the molecular level.

Indexed as

AnimalsBody PatterningCaenorhabditis elegansEmbryo, NonmammalianAdhesionC. elegansCell migrationContractilityMorphogenesisPolarityRosettes

Identifiers

PMID33309948
PMCPMC8597047
OpenAlexW3111631623

What Socratic holds

Textmetadata
LicenceTDM
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.