Evidence map›Paper›PMID 39052672›Full record

ArticlePLoS genetics2024

Maternal regulation of the vertebrate oocyte-to-embryo transition.

Ricardo Fuentes, Florence L Marlow, Elliott W Abrams, Hong Zhang, Manami Kobayashi, Tripti Gupta, Lee D Kapp, Zachary DiNardo, Ronald Heller, Ruth Cisternas and 7 more

Abstract read
In one paragraph

Article in PLoS genetics, 2024. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. 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

17 authors.

Ricardo FuentesDepartment of Cell and Developmental Biology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0000-0002-3378-0299
Florence L MarlowDepartment of Cell and Developmental Biology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, United States of America.
Elliott W AbramsDepartment of Cell and Developmental Biology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0000-0002-8866-8421
Hong ZhangDepartment of Cell and Developmental Biology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, United States of America.
Manami KobayashiDepartment of Cell and Developmental Biology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, United States of America.
Tripti GuptaDepartment of Cell and Developmental Biology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, United States of America.
Lee D KappDepartment of Cell and Developmental Biology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0009-0006-6005-6630
Zachary DiNardoDepartment of Cell and Developmental Biology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0009-0008-3128-3986
Ronald HellerDepartamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile.
Ruth CisternasDepartamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile.
Priscila García-CastroDepartamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile.
Fabián Segovia-MirandaDepartamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile.ORCID https://orcid.org/0000-0003-1546-0475
Felipe Montecinos-FranjolaLaboratory of Cell Structure and Dynamics, National Institute on Deafness and Other Communication Disorders (NIDCD), National Institutes of Health, Bethesda, Maryland, United States of America.ORCID https://orcid.org/0000-0002-1823-103X
William VoughtDepartment of Cell and Developmental Biology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, United States of America.
Charles E VejnarDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut, United States of America.
Antonio J GiraldezDepartment of Genetics, Yale University School of Medicine, New Haven, Connecticut, United States of America.
Mary C MullinsDepartment of Cell and Developmental Biology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0000-0002-9979-1564

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Molecular mechanisms of the maternal to zygotic transitionR35GM122580 · NIGMS · YALE UNIVERSITY · PI Antonio J Giraldez · 2017 to 2026
$8.1M
TRAINING PROGRAM IN DEVELOPMENTAL BIOLOGYT32HD007516 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI RAPER, JONATHAN A · 1998 to 2012
$5.6M
Oocyte polarity and BMP-mediated dorsoventral patterningR35GM131908 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI Mary C. Mullins · 2019 to 2026
$5.6M
Adult genome-wide phenotypic analysis of molecularly defined mutant genesR01HD069321 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI MULLINS, MARY C. · 2011 to 2015
$3.1M
Deciphering the regulatory code that specifies different cell fates in development using single cell genomicsR01HD100035 · NICHD · YALE UNIVERSITY · PI GIRALDEZ, ANTONIO J, KRISHNASWAMY, SMITA · 2020 to 2024
$2.8M
Functional analysis of the zebrafish genome through RNA-seq and ribosome profileR01HD074078 · NICHD · YALE UNIVERSITY · PI GIRALDEZ, ANTONIO J · 2012 to 2016
$2.3M
Multimodal Analysis of the Genome Architecture Using Expansion MicroscopyR01HG012969 · NHGRI · YALE UNIVERSITY · PI Joerg Bewersdorf, Antonio J Giraldez · 2024 to 2026
$2.1M
Analysis of the gene networks regulating the maternal to zygotic transitionR01GM103789 · NIGMS · YALE UNIVERSITY · PI GIRALDEZ, ANTONIO J · 2012 to 2015
$1.7M
Molecular Identity of Maternal Regulators of the Egg to Embryo TransitionR21HD094096 · NICHD · UNIVERSITY OF PENNSYLVANIA · PI MULLINS, MARY C. · 2017 to 2018
$443k
Regulating the mid-blastula transition in zebrafishF32GM077835 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI ABRAMS, ELLIOTT W · 2006 to 2007
$99k
Maternal Control of Ventral Cell Fate Specification in the ZebrafishF32GM080926 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI KAPP, LEE · 2007 to 2008
$96k
NCATS NIH HHS UL1 TR001863NHGRI NIH HHS R01 HG012969NICHD NIH HHS R01 HD069321NICHD NIH HHS R01 HD074078NICHD NIH HHS R01 HD100035NICHD NIH HHS R21 HD094096NICHD NIH HHS T32 HD007516NIGMS NIH HHS F32 GM077835NIGMS NIH HHS F32 GM080926NIGMS NIH HHS R01 GM103789NIGMS NIH HHS R35 GM122580NIGMS NIH HHS R35 GM131908
6 · The paper itself

Abstract

Maternally-loaded factors in the egg accumulate during oogenesis and are essential for the acquisition of oocyte and egg developmental competence to ensure the production of viable embryos. However, their molecular nature and functional importance remain poorly understood. Here, we present a collection of 9 recessive maternal-effect mutants identified in a zebrafish forward genetic screen that reveal unique molecular insights into the mechanisms controlling the vertebrate oocyte-to-embryo transition. Four genes, over easy, p33bjta, poached and black caviar, were found to control initial steps in yolk globule sizing and protein cleavage during oocyte maturation that act independently of nuclear maturation. The krang, kazukuram, p28tabj, and spotty genes play distinct roles in egg activation, including cortical granule biology, cytoplasmic segregation, the regulation of microtubule organizing center assembly and microtubule nucleation, and establishing the basic body plan. Furthermore, we cloned two of the mutant genes, identifying the over easy gene as a subunit of the Adaptor Protein complex 5, Ap5m1, which implicates it in regulating intracellular trafficking and yolk vesicle formation. The novel maternal protein Krang/Kiaa0513, highly conserved in metazoans, was discovered and linked to the function of cortical granules during egg activation. These mutant genes represent novel genetic entry points to decipher the molecular mechanisms functioning in the oocyte-to-embryo transition, fertility, and human disease. Additionally, our genetic adult screen not only contributes to the existing knowledge in the field but also sets the basis for future investigations. Thus, the identified maternal genes represent key players in the coordination and execution of events prior to fertilization.

Indexed as

OocytesOogenesisZebrafishZebrafish ProteinsAnimalsEmbryonic DevelopmentEmbryo, NonmammalianFemaleGene Expression Regulation, DevelopmentalMaternal InheritanceMutationZebrafish Proteins

Identifiers

PMID39052672
PMCPMC11302925

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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.