Evidence map›Paper›PMID 30799226›Full record

ArticleDevelopmental cell2019

Maternal Ribosomes Are Sufficient for Tissue Diversification during Embryonic Development in C. elegans.

Elif Sarinay Cenik, Xuefeng Meng, Ngang Heok Tang, Richard Nelson Hall, Joshua A Arribere, Can Cenik, Yishi Jin, Andrew Fire

Open access · greenAbstract read
In one paragraph

Article in Developmental cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

43 citing papers in PubMed, 64 citations in OpenAlex.

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  14. Assessing Human Ribosomal DNA Variation and Its Association With Phenotypic Outcomes.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  15. Landscape and regulation of mRNA translation in the earlybioRxiv : the preprint server for biology · 2025
    Article
  16. Specialized ribosomes: integrating new insights and current challenges.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  17. Article
  18. Article
  19. High-resolution reconstruction of aRNA (New York, N.Y.) · 2024
    Article
  20. A dual ribosomal system in the zebrafish soma and germline.bioRxiv : the preprint server for biology · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Elif Sarinay CenikDepartment of Pathology, Stanford University Medical School, Stanford, CA, USA; Department of Molecular Biosciences, University of Texas Austin, Austin, TX, USA.
Xuefeng MengDepartment of Cellular and Molecular Medicine, School of Medicine, University of California, San Diego, San Diego, CA, USA.
Ngang Heok TangDepartment of Cellular and Molecular Medicine, School of Medicine, University of California, San Diego, San Diego, CA, USA.
Richard Nelson HallDepartment of Bioengineering, Stanford University, Stanford, CA, USA.
Joshua A ArribereDepartment of MCD Biology, University of California, Santa Cruz, Santa Cruz, CA, USA.
Can CenikDepartment of Molecular Biosciences, University of Texas Austin, Austin, TX, USA.
Yishi JinDepartment of Cellular and Molecular Medicine, School of Medicine, University of California, San Diego, San Diego, CA, USA.
Andrew FireDepartment of Pathology, Stanford University Medical School, Stanford, CA, USA. Electronic address: afire@stanford.edu.
University of California San Diego · USThe University of Texas at Austin · USStanford Medicine · USStanford University · USUniversity of California, Santa Cruz · US

Funding

GENE REGULATION DURING EARLY DEVELOPMENT OF C. ELEGANSR01GM037706 · NIGMS · STANFORD UNIVERSITY · PI FIRE, ANDREW Z. · 1987 to 2018
$11.0M
GABAERGIC NEURON DIFFERENTIATION IN C ELEGANSR01NS035546 · NINDS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI JIN, YISHI · 1996 to 2016
$5.3M
Cellular Response to Genetic ChangeR35GM130366 · NIGMS · STANFORD UNIVERSITY · PI ANDREW Z. FIRE · 2019 to 2026
$4.8M
GABAergic Neuron Differentiation in C.elegansR37NS035546 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JIN, YISHI · 2017 to 2021
$2.4M
NIGMS NIH HHS R01 GM037706NIGMS NIH HHS R35 GM130366NINDS NIH HHS R01 NS035546NINDS NIH HHS R37 NS035546
6 · The paper itself

Abstract

Caenorhabditis elegans provides an amenable system to explore whether newly composed ribosomes are required to progress through development. Despite the complex pattern of tissues that are formed during embryonic development, we found that null homozygotes lacking any of the five different ribosomal proteins (RPs) can produce fully functional first-stage larvae, with similar developmental competence seen upon complete deletion of the multi-copy ribosomal RNA locus. These animals, relying on maternal but not zygotic contribution of ribosomal components, are capable of completing embryogenesis. In the absence of new ribosomal components, the resulting animals are arrested before progression from the first larval stage and fail in two assays for postembryonic plasticity of neuronal structure. Mosaic analyses of larvae that are a mixture of ribosome-competent and non-competent cells suggest a global regulatory mechanism in which ribosomal insufficiency in a subset of cells triggers organism-wide growth arrest.

Indexed as

Embryonic DevelopmentOrganogenesisAnimalsBase SequenceCaenorhabditis elegansCaenorhabditis elegans ProteinsFemaleGene Expression Regulation, DevelopmentalLarvaMosaicismMutationPhenotypeRibosomal ProteinsRibosomesRNA, RibosomalTranscription, GeneticCaenorhabditis elegans ProteinsRibosomal ProteinsRNA, RibosomalCaenorhabditis eleganscell non-autonomouscheckpointembryomaternalrDNA locusribosomes

Identifiers

PMID30799226
PMCPMC6582967
OpenAlexW2915191659

What OpenQuestion 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 OpenQuestion graph.