Evidence map›Paper›PMID 24741069›Full record

ArticleJournal of cell science2014

The dynamics of MAPK inactivation at fertilization in mouse eggs.

Jose Raul Gonzalez-Garcia, Josephine Bradley, Michail Nomikos, Laboni Paul, Zoltan Machaty, F Anthony Lai, Karl Swann

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. The signal that stimulates mammalian embryo development.Frontiers in cell and developmental biology · 2024
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. 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

7 authors at 2 institutions in 2 countries.

Jose Raul Gonzalez-GarciaInstitute of Molecular and Experimental Medicine, School of Medicine, Cardiff University, Cardiff CF14 4XN, UK.
Josephine BradleyInstitute of Molecular and Experimental Medicine, School of Medicine, Cardiff University, Cardiff CF14 4XN, UK School of Biosciences, Cardiff University, Cardiff CF10 3AX, UK.
Michail NomikosInstitute of Molecular and Experimental Medicine, School of Medicine, Cardiff University, Cardiff CF14 4XN, UK.
Laboni PaulInstitute of Molecular and Experimental Medicine, School of Medicine, Cardiff University, Cardiff CF14 4XN, UK School of Biosciences, Cardiff University, Cardiff CF10 3AX, UK.
Zoltan MachatyDepartment of Animal Sciences, Purdue University, West Lafayette, IN 47907, USA.
F Anthony LaiInstitute of Molecular and Experimental Medicine, School of Medicine, Cardiff University, Cardiff CF14 4XN, UK.
Karl SwannInstitute of Molecular and Experimental Medicine, School of Medicine, Cardiff University, Cardiff CF14 4XN, UK swannk1@cf.ac.uk.
Cardiff University · GBPurdue University West Lafayette · US

Funding

Wellcome Trust
6 · The paper itself

Abstract

Egg activation at fertilization in mammals is initiated by prolonged Ca(2+) oscillations that trigger the completion of meiosis and formation of pronuclei. A fall in mitogen-activated protein kinase (MAPK) activity is essential for pronuclear formation, but the precise timing and mechanism of decline are unknown. Here, we have measured the dynamics of MAPK pathway inactivation during fertilization of mouse eggs using novel chemiluminescent MAPK activity reporters. This reveals that the MAPK activity decrease begins during the Ca(2+) oscillations, but MAPK does not completely inactivate until after pronuclear formation. The MAPKs present in eggs are Mos, MAP2K1 and MAP2K2 (MEK1 and MEK2, respectively) and MAPK3 and MAPK1 (ERK1 and ERK2, respectively). Notably, the MAPK activity decline at fertilization is not explained by upstream destruction of Mos, because a decrease in the signal from a Mos-luciferase reporter is not associated with egg activation. Furthermore, Mos overexpression does not affect the timing of MAPK inactivation or pronuclear formation. However, the late decrease in MAPK could be rapidly reversed by the protein phosphatase inhibitor, okadaic acid. These data suggest that the completion of meiosis in mouse zygotes is driven by an increased phosphatase activity and not by a decline in Mos levels or MEK activity.

Indexed as

AnimalsCalcium SignalingEnzyme InhibitorsFemaleFertilizationGenes, ReporterLuciferases, RenillaMaleMiceMice, Inbred C57BLMice, Inbred CBAMitogen-Activated Protein KinasesOkadaic AcidOncogene Proteins v-mosOvumPhosphoric Monoester HydrolasesEnzyme InhibitorsLuciferases, RenillaMitogen-Activated Protein KinasesOkadaic AcidOncogene Proteins v-mosPhosphoric Monoester HydrolasesEggFertilizationMAPKZygote

Identifiers

PMID24741069
PMCPMC4058113
OpenAlexW2143948352

What OpenQuestion 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 OpenQuestion graph.