Evidence map›Paper›PMID 32347793›Full record

ArticleeLife2020

Maternal spindle transfer overcomes embryo developmental arrest caused by ooplasmic defects in mice.

Nuno Costa-Borges, Katharina Spath, Irene Miguel-Escalada, Enric Mestres, Rosa Balmaseda, Anna Serafín, Maria Garcia-Jiménez, Ivette Vanrell, Jesús González, Klaus Rink and 2 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 5% 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

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

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Pronuclear Transfer and Maternal Spindle Transfer in the Mouse.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Mitochondrial Genetic Drift after Nuclear Transfer in Oocytes.International journal of molecular sciences · 2020
    Review
  16. Review
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

12 authors at 3 institutions in 2 countries.

Nuno Costa-BorgesEmbryotools, Parc Cientific de Barcelona, Barcelona, Spain.ORCID 0000-0002-2073-7515
Katharina SpathNuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom.
Irene Miguel-EscaladaGenomics and Bioinformatics, Centre for Genomic Regulation, Barcelona, Spain.ORCID 0000-0003-3461-6404
Enric MestresEmbryotools, Parc Cientific de Barcelona, Barcelona, Spain.ORCID 0000-0001-6140-6416
Rosa BalmasedaPCB Animal Facility, Parc Cientific de Barcelona, Barcelona, Spain.
Anna SerafínPCB Animal Facility, Parc Cientific de Barcelona, Barcelona, Spain.
Maria Garcia-JiménezEmbryotools, Parc Cientific de Barcelona, Barcelona, Spain.ORCID 0000-0003-3321-8869
Ivette VanrellEmbryotools, Parc Cientific de Barcelona, Barcelona, Spain.
Jesús GonzálezPCB Animal Facility, Parc Cientific de Barcelona, Barcelona, Spain.
Klaus RinkEmbryotools, Parc Cientific de Barcelona, Barcelona, Spain.
Dagan WellsNuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom.
Gloria CalderónEmbryotools, Parc Cientific de Barcelona, Barcelona, Spain.ORCID 0000-0003-3235-0323
Barcelona Biomedical Research Park · ESUniversity of Oxford · GBCentre for Genomic Regulation · ES

Funding

Causes and consequences of mitochondrial dysfunction in oocytes and cumulus cellsR01HD092550 · NICHD · BRIGHAM AND WOMEN'S HOSPITAL · PI GINSBURG, ELIZABETH S, RACOWSKY, CATHERINE · 2017 to 2021
$2.6M
European Regional Development Fund RD-15-1-0011NICHD NIH HHS R01 HD092550NIH HHS 1R01HD092550-01
6 · The paper itself

Abstract

The developmental potential of early embryos is mainly dictated by the quality of the oocyte. Here, we explore the utility of the maternal spindle transfer (MST) technique as a reproductive approach to enhance oocyte developmental competence. Our proof-of-concept experiments show that replacement of the entire cytoplasm of oocytes from a sensitive mouse strain overcomes massive embryo developmental arrest characteristic of non-manipulated oocytes. Genetic analysis confirmed minimal carryover of mtDNA following MST. Resulting mice showed low heteroplasmy levels in multiple organs at adult age, normal histology and fertility. Mice were followed for five generations (F5), revealing that heteroplasmy was reduced in F2 mice and was undetectable in the subsequent generations. This pre-clinical model demonstrates the high efficiency and potential of the MST technique, not only to prevent the transmission of mtDNA mutations, but also as a new potential treatment for patients with certain forms of infertility refractory to current clinical strategies.

Indexed as

AnimalsDNA, MitochondrialEmbryonic DevelopmentFemaleMiceMitochondrial Replacement TherapyMutationOocytesPregnancyDNA, Mitochondrialcell biologydevelopmental biologyembryo developmentheteroplasmyInfertilitymitochondrial DNAmouseoocytesSpindle transfer

Identifiers

PMID32347793
PMCPMC7259950
OpenAlexW3019458629

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.