Evidence map›Paper›PMID 23852387›Full record

ArticleGenetics2013

Association of maternal mRNA and phosphorylated EIF4EBP1 variants with the spindle in mouse oocytes: localized translational control supporting female meiosis in mammals.

Edward J Romasko, Dasari Amarnath, Uros Midic, Keith E Latham

Abstract read
In one paragraph

Article in Genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 45 citations in OpenAlex.

  1. Declining ribosome function limits oocyte longevity.bioRxiv : the preprint server for biology · 2026
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  17. Role of mTOR Signaling in Female Reproduction.Frontiers in endocrinology · 2019
    Review
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  20. 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.

Edward J RomaskoFels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140.
Dasari Amarnath
Uros Midic
Keith E Latham
Temple University · US

Funding

The Primate Embryo Gene Expression ResourceR24RR015253 · NCRR · TEMPLE UNIV OF THE COMMONWEALTH · PI LATHAM, KEITH E · 2000 to 2011
$4.9M
Primate Embryo Gene Expression ResourceR24OD012221 · OD · TEMPLE UNIV OF THE COMMONWEALTH · PI LATHAM, KEITH E · 2012 to 2016
$3.0M
Nuclear Reprogramming and Phenotype in Cloned EmbryosR01HD043092 · NICHD · TEMPLE UNIV OF THE COMMONWEALTH · PI LATHAM, KEITH E · 2003 to 2013
$3.0M
Genetic and Molecular Approach to Identify Ooplasm Reprogramming FactorsRC1HD063371 · NICHD · TEMPLE UNIV OF THE COMMONWEALTH · PI LATHAM, KEITH E · 2009 to 2010
$1.0M
NCRR NIH HHS R24 RR015253NCRR NIH HHS R24RR015253NICHD NIH HHS R01 HD043092NICHD NIH HHS R01-HD43092NICHD NIH HHS RC1 HD063371NICHD NIH HHS RC1-HD063371-02NIH HHS R24 OD-012221NIH HHS R24 OD012221
6 · The paper itself

Abstract

In contrast to other species, localized maternal mRNAs are not believed to be prominent features of mammalian oocytes. We find by cDNA microarray analysis enrichment for maternal mRNAs encoding spindle and other proteins on the mouse oocyte metaphase II (MII) spindle. We also find that the key translational regulator, EIF4EBP1, undergoes a dynamic and complex spatially regulated pattern of phosphorylation at sites that regulate its association with EIF4E and its ability to repress translation. These phosphorylation variants appear at different positions along the spindle at different stages of meiosis. These results indicate that dynamic spatially restricted patterns of EIF4EBP1 phosphorylation may promote localized mRNA translation to support spindle formation, maintenance, function, and other nearby processes. Regulated EIF4EBP1 phosphorylation at the spindle may help coordinate spindle formation with progression through the cell cycle. The discovery that EIF4EBP1 may be part of an overall mechanism that integrates and couples cell cycle progression to mRNA translation and subsequent spindle formation and function may be relevant to understanding mechanisms leading to diminished oocyte quality, and potential means of avoiding such defects. The localization of maternal mRNAs at the spindle is evolutionarily conserved between mammals and other vertebrates and is also seen in mitotic cells, indicating that EIF4EBP1 control of localized mRNA translation is likely key to correct segregation of genetic material across cell types.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCarrier ProteinsCell CycleCell Cycle ProteinsEukaryotic Initiation Factor-4EEukaryotic Initiation FactorsFemaleMeiosisMiceMicrotubulesOligonucleotide Array Sequence AnalysisOocytesPhosphoproteinsPhosphorylationRNA, MessengerAdaptor Proteins, Signal TransducingCarrier ProteinsCell Cycle ProteinsEif4ebp1 protein, mouseEukaryotic Initiation Factor-4EEukaryotic Initiation FactorsPhosphoproteinsRNA, Messengercell cyclelocalized maternal mRNAmeiosis, spindleMicroarrayprotein phosphorylationtranslational control

Identifiers

PMID23852387
PMCPMC3781964
OpenAlexW2130255559

What OpenQuestion holds

Textmetadata
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.