Evidence map›Paper›PMID 19551325›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2009

Oocytes and early embryos selectively express the survival factor BCL2L10.

Yannis Guillemin, Philippe Lalle, Germain Gillet, Jean-François Guerin, Samir Hamamah, Abdel Aouacheria

Abstract read
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In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 4% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Molecular Characterization and Expression Changes of theCurrent issues in molecular biology · 2024
    Article
  4. Review
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  6. Review
  7. A balanced translocation disrupting BCL2L10 and PNLDC1 segregates with affective psychosis.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2017
    Article
  8. Article
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  12. Differentially expressed micoRNAs in human oocytes.Journal of assisted reproduction and genetics · 2011
    Article
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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

6 authors at 5 institutions in 1 country.

Yannis GuilleminIBCP, Institut de Biologie et Chimie des Protéines, CNRS, UMR 5086 Université de Lyon 1, IFR 128, CNRS, IBCP, 7 passage du Vercors, Lyon, F-69367, France.
Philippe Lalle
Germain Gillet
Jean-François Guerin
Samir Hamamah
Abdel Aouacheria
Université Claude Bernard Lyon 1 · FRCentre National de la Recherche Scientifique · FRDélégation Régionale Auvergne-Rhône-Alpes · FRInserm · FRInstitut de Biologie et de Chimie des Protéines · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Apoptosis has been reported in oocytes and human preimplantation embryos both in vitro and in vivo. BCL-2 family proteins are likely to play a pivotal role in controlling oocyte and early embryo degeneration. However, no BCL-2-related survival factors have been identified that would specifically function during oocyte maturation, after fertilization and during early embryogenesis. Here, we performed a comprehensive tissue expression pattern analysis of the BCL-2 family at the mRNA level. While expression of various members was detected in human oocytes and during early primate embryogenesis, our data indicate that BCL2L10 is the predominant maternally loaded Bcl-2 family transcript, revealing an evolutionary conserved expression profile at the egg-to-zygote transition. We provide evidence that BCL2L10 is associated with the microtubule binding protein translationally controlled tumor protein and mitochondria, with a stage-specific redistribution along the pericortical regulatory ooplasm. In dying oocytes, BCL2L10 colocalized with proapoptotic BAX and neutralization of BCL2L10 accelerated oocyte death. We propose BCL2L10 as a novel and prime candidate related to oocyte maturation, fertility, and embryo developmental competence.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsCell DeathEmbryo, MammalianEmbryonic DevelopmentHumansMiceMitochondrial ProteinsOocytesProto-Oncogene Proteins c-bcl-2Tissue DistributionBCL2-like 10 proteinMitochondrial ProteinsProto-Oncogene Proteins c-bcl-2

Identifiers

PMID19551325
OpenAlexW2038106756

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.