Evidence map›Paper›PMID 21460039›Full record

ArticleGenes & development2011

Genome-wide analysis of translation reveals a critical role for deleted in azoospermia-like (Dazl) at the oocyte-to-zygote transition.

Jing Chen, Collin Melton, Nayoung Suh, Jeong Su Oh, Kathleen Horner, Fang Xie, Claudio Sette, Robert Blelloch, Marco Conti

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 153 papers.

0numbers the graph read from it
0cells of the map it votes in
153citing 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

153 citing papers in PubMed, 263 citations in OpenAlex.

  1. Article
  2. Translational Fidelity Decline in the Aging Oocyte and Embryo Development.International journal of molecular sciences · 2026
    Review
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93 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 2 countries.

Jing ChenCenter for Reproductive Sciences, University of California at San Francisco, San Francisco, California 94143, USA.
Collin Melton
Nayoung Suh
Jeong Su Oh
Kathleen Horner
Fang Xie
Claudio Sette
Robert Blelloch
Marco Conti
Broad Center · USUniversity of California, San Francisco · USFondazione Santa Lucia · IT

Funding

Trophoblast Differentiation in In Vivo and In Vitro Fertilized EmbryosU54HD055764 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BLELLOCH, ROBERT · 2007 to 2013
$11.5M
Role of the EGF Network in OvulationR01HD052909 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CONTI, MARCO · 2007 to 2011
$1.7M
Small RNAs in Stem Cell Differentiation and Neural DevelopmentR01NS057221 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BLELLOCH, ROBERT · 2007 to 2010
$1.4M
Cyclic AMP and the Control of the Meiotic Cell CycleR01GM080527 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CONTI, MARCO · 2007 to 2010
$1.2M
Determinants of Neural &Embryonic Stem Cell PotencyK08NS048118 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BLELLOCH, ROBERT · 2005 to 2009
$876k
NICHD NIH HHS R01 HD052909NICHD NIH HHS R01HD052909NICHD NIH HHS U54 HD055764NICHD NIH HHS U54-HD055764NIGMS NIH HHS R01 GM080527NIGMS NIH HHS R01-GM080527NINDS NIH HHS K08 NS048118NINDS NIH HHS K08 NS48118NINDS NIH HHS R01 NS057221NINDS NIH HHS R01NS057221PHS HHS U54-D055764Telethon GGP09154
6 · The paper itself

Abstract

Oocyte maturation, fertilization, and early embryonic development occur in the absence of gene transcription. Therefore, it is critical to understand at a global level the post-transcriptional events that are driving these transitions. Here we used a systems approach by combining polysome mRNA profiling and bioinformatics to identify RNA-binding motifs in mRNAs that either enter or exit the polysome pool during mouse oocyte maturation. Association of mRNA with the polysomes correlates with active translation. Using this strategy, we identified highly specific patterns of mRNA recruitment to the polysomes that are synchronized with the cell cycle. A large number of the mRNAs recovered with translating ribosomes contain motifs for the RNA-binding proteins DAZL (deleted in azoospermia-like) and CPEB (cytoplasmic polyadenylation element-binding protein). Although a Dazl role in early germ cell development is well established, no function has been described during oocyte-to-embryo transition. We demonstrate that CPEB1 regulates Dazl post-transcriptionally, and that DAZL is essential for meiotic maturation and embryonic cleavage. In the absence of DAZL synthesis, the meiotic spindle fails to form due to disorganization of meiotic microtubules. Therefore, Cpeb1 and Dazl function in a progressive, self-reinforcing pathway to promote oocyte maturation and early embryonic development.

Indexed as

Gene Expression RegulationGenome-Wide Association Study3' Untranslated RegionsAnimalsEmbryo, MammalianMiceOocytesPolyribosomesRNA-Binding ProteinsZygote3' Untranslated RegionsDAZL protein, mouseRNA-Binding Proteins

Identifiers

PMID21460039
PMCPMC3070937
OpenAlexW2133482368

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.