Evidence map›Paper›PMID 27664515›Full record

ArticleComparative biochemistry and physiology. Toxicology & pharmacology : CBP2017

Zinc availability during germline development impacts embryo viability in Caenorhabditis elegans.

Adelita D Mendoza, Teresa K Woodruff, Sarah M Wignall, Thomas V O'Halloran

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Quantifying Embryonic Lethality Rate in Caenorhabditis elegans.Journal of visualized experiments : JoVE · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Role of zinc in female reproduction.Biology of reproduction · 2021
    Review
  10. Article
  11. Review
  12. Zinc homeostasis and signaling in the roundworm C. elegans.Biochimica et biophysica acta. Molecular cell research · 2021
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. 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

4 authors at 1 institution in 1 country.

Adelita D MendozaDepartment of Molecular Biosciences, Northwestern University, Evanston, IL 60208, USA; The Chemistry of Life Processes Institute, Northwestern University, Evanston, IL 60208, USA.
Teresa K WoodruffDepartment of Molecular Biosciences, Northwestern University, Evanston, IL 60208, USA; The Chemistry of Life Processes Institute, Northwestern University, Evanston, IL 60208, USA; Department of Obstetrics and Gynecology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Sarah M WignallDepartment of Molecular Biosciences, Northwestern University, Evanston, IL 60208, USA. Electronic address: s-wignall@northwestern.edu.
Thomas V O'HalloranDepartment of Molecular Biosciences, Northwestern University, Evanston, IL 60208, USA; The Chemistry of Life Processes Institute, Northwestern University, Evanston, IL 60208, USA; Department of Chemistry, Northwestern University, Evanston, IL 60208, USA. Electronic address: t-ohalloran@northwestern.edu.
Northwestern University · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Northwestern University Clinical and Translational Science Institute (NUCATS)UL1TR001422 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2015 to 2023
$56.8M
CARCINOGENESIS TRAINING PROGRAMT32CA009560 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Kathleen Janee Green · 1986 to 2026
$8.4M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Mentoring For Success: Developing Fundamental Skills For Biomedical ResearchR25GM079300 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MCGEE, RICHARD · 2007 to 2020
$6.6M
METALLOREGULATION BY MERR AND FUR PROTEIN FAMILIESR37GM038784 · NIGMS · NORTHWESTERN UNIVERSITY · PI O'HALLORAN, THOMAS V · 2001 to 2010
$3.6M
Metalloregulation by MerR and Fur Protein FamiliesR01GM038784 · NIGMS · NORTHWESTERN UNIVERSITY · PI O'HALLORAN, THOMAS V · 1992 to 2025
$3.5M
Regulatory Roles of Zinc Fluxes in Metalloprotein Occupancy and Cell Cycle ProgressionR01GM115848 · NIGMS · NORTHWESTERN UNIVERSITY · PI O'HALLORAN, THOMAS V · 2015 to 2025
$2.8M
Zinc Regulation of Germline and Embryo Development in Caenorhabditis elegansF31GM112478 · NIGMS · NORTHWESTERN UNIVERSITY · PI MENDOZA, ADELITA D. · 2014 to 2016
$109k
NCATS NIH HHS UL1 TR001422NCI NIH HHS P30 CA060553NCI NIH HHS T32 CA009560NIGMS NIH HHS F31 GM112478NIGMS NIH HHS R01 GM038784NIGMS NIH HHS R01 GM115848NIGMS NIH HHS R25 GM079300NIGMS NIH HHS R37 GM038784NIH HHS P40 OD010440
6 · The paper itself

Abstract

Zinc is an essential metal that serves as a cofactor in a variety of cellular processes, including meiotic maturation. Cellular control of zinc uptake, availability and efflux is closely linked to meiotic progression in rodent and primate reproduction where large fluctuations in zinc levels are critical at several steps in the oocyte-to-embryo transition. Despite these well-documented roles of zinc fluxes during meiosis, only a few of the genes encoding key zinc receptors, membrane-spanning transporters, and downstream signaling pathway factors have been identified to date. Furthermore, little is known about analogous roles for zinc fluxes in the context of a whole organism. Here, we evaluate whether zinc availability regulates germline development and oocyte viability in the nematode Caenorhabditis elegans, an experimentally flexible model organism. We find that similar to mammals, mild zinc limitation in C. elegans profoundly impacts the reproductive axis: the brood size is significantly reduced under conditions of zinc limitation where other physiological functions are not perturbed. Zinc limitation in this organism has a more pronounced impact on oocytes than sperm and this leads to the decrease in viable embryo production. Moreover, acute zinc limitation of isolated zygotes prevents extrusion of the second polar body during meiosis and leads to aneuploid embryos. Thus, the zinc-dependent steps in C. elegans gametogenesis roughly parallel those described in meiotic-to-mitotic transitions in mammals.

Indexed as

GametogenesisAneuploidyAnimalsAnimals, Genetically ModifiedCaenorhabditis elegansCell SurvivalChelating AgentsChromosome SegregationEmbryo, NonmammalianEthylaminesFemaleGenotypeMaleOocytesPhenotypePyridinesChelating AgentsEthylaminesN,N,N',N'-tetrakis(2-pyridylmethyl)ethane-1,2-diaminePyridinesZinc

Identifiers

PMID27664515
PMCPMC5210184
OpenAlexW2522802817

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.