Evidence map›Paper›PMID 24957527›Full record

ArticleThe EMBO journal2014

Global characterization of the oocyte-to-embryo transition in Caenorhabditis elegans uncovers a novel mRNA clearance mechanism.

Marlon Stoeckius, Dominic Grün, Marieluise Kirchner, Salah Ayoub, Francesca Torti, Fabio Piano, Margareta Herzog, Matthias Selbach, Nikolaus Rajewsky

Abstract read
In one paragraph

Article in The EMBO journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing 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

55 citing papers in PubMed.

  1. Article
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  3. Article
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  5. Article
  6. Article
  7. Article
  8. Landscape and regulation of mRNA translation in the earlybioRxiv : the preprint server for biology · 2025
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. A spatiotemporally resolved atlas of mRNA decay in thebioRxiv : the preprint server for biology · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. A Compilation of the Diverse miRNA Functions inInternational journal of molecular sciences · 2023
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Marlon StoeckiusSystems Biology of Gene Regulatory Elements, Max Delbrück Center Berlin, Berlin, Germany.
Dominic GrünSystems Biology of Gene Regulatory Elements, Max Delbrück Center Berlin, Berlin, Germany.
Marieluise KirchnerCell Signalling and Mass Spectrometry, Max Delbrück Center Berlin, Berlin, Germany.
Salah AyoubSystems Biology of Gene Regulatory Elements, Max Delbrück Center Berlin, Berlin, Germany.
Francesca TortiSystems Biology of Gene Regulatory Elements, Max Delbrück Center Berlin, Berlin, Germany.
Fabio PianoCenter for Genomics and Systems Biology, Department of Biology New York University, New York, NY, USA Division of Science, New York University Abu Dhabi, Abu Dhabi, United Arab Emirates.
Margareta HerzogSystems Biology of Gene Regulatory Elements, Max Delbrück Center Berlin, Berlin, Germany.
Matthias SelbachCell Signalling and Mass Spectrometry, Max Delbrück Center Berlin, Berlin, Germany.
Nikolaus RajewskySystems Biology of Gene Regulatory Elements, Max Delbrück Center Berlin, Berlin, Germany rajewsky@mdc-berlin.de.

Funding

A Systematic RNAi-based Map of C. elegans EmbryogenesisR01HD046236 · NICHD · NEW YORK UNIVERSITY · PI GUNSALUS, KRISTIN C, PIANO, FABIO · 2004 to 2013
$4.5M
NICHD NIH HHS R01 HD046236NICHD NIH HHS R01HD046236
6 · The paper itself

Abstract

The oocyte-to-embryo transition (OET) is thought to be mainly driven by post-transcriptional gene regulation. However, expression of both RNAs and proteins during the OET has not been comprehensively assayed. Furthermore, specific molecular mechanisms that regulate gene expression during OET are largely unknown. Here, we quantify and analyze transcriptome-wide, expression of mRNAs and thousands of proteins in Caenorhabditis elegans oocytes, 1-cell, and 2-cell embryos. This represents a first comprehensive gene expression atlas during the OET in animals. We discovered a first wave of degradation in which thousands of mRNAs are cleared shortly after fertilization. Sequence analysis revealed a statistically highly significant presence of a polyC motif in the 3' untranslated regions of most of these degraded mRNAs. Transgenic reporter assays demonstrated that this polyC motif is required and sufficient for mRNA degradation after fertilization. We show that orthologs of human polyC-binding protein specifically bind this motif. Our data suggest a mechanism in which the polyC motif and binding partners direct degradation of maternal mRNAs. Our data also indicate that endogenous siRNAs but not miRNAs promote mRNA clearance during the OET.

Indexed as

RNA Stability3' Untranslated RegionsAnimalsAnimals, Genetically ModifiedCaenorhabditis elegansCaenorhabditis elegans ProteinsEmbryo, NonmammalianFemaleFertilizationGene Expression ProfilingGene Expression Regulation, DevelopmentalMicroRNAsOocytesPoly CProteomeRNA-Binding Proteins3' Untranslated RegionsCaenorhabditis elegans ProteinsMicroRNAsPoly CProteomeRNA-Binding ProteinsRNA, Messenger, StoredRNA, Small InterferingCaenorhabditis elegansembryogenesismaternal mRNAoocyte‐to‐embryo transitionposttranscriptional gene regulation

Identifiers

PMID24957527
PMCPMC4195759

What OpenQuestion holds

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Registered trials

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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.