Evidence map›Paper›PMID 32381741›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Oocytes can efficiently repair DNA double-strand breaks to restore genetic integrity and protect offspring health.

Jessica M Stringer, Amy Winship, Nadeen Zerafa, Matthew Wakefield, Karla Hutt

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
7.7field-weighted citation impact, top 2% 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

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 129 citations in OpenAlex.

  1. Pooled it
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  7. Review
  8. Article
  9. The inflammatory clock: how cGAS-STING ticks in the aging ovary.Frontiers in cell and developmental biology · 2026
    Review
  10. Article
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  12. Article
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  16. Premature ovarian insufficiency.Nature reviews. Disease primers · 2024
    Review
  17. Article
  18. Article
  19. Article
  20. Article

1 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

5 authors at 2 institutions in 1 country.

Jessica M StringerOvarian Biology Laboratory, Biomedicine Discovery Institute, Monash University, Melbourne 3800, Australia.
Amy WinshipOvarian Biology Laboratory, Biomedicine Discovery Institute, Monash University, Melbourne 3800, Australia.ORCID 0000-0001-7848-1447
Nadeen ZerafaOvarian Biology Laboratory, Biomedicine Discovery Institute, Monash University, Melbourne 3800, Australia.
Matthew WakefieldDepartment of Obstetrics and Gynaecology, University of Melbourne, Royal Women's Hospital, Parkville, Victoria 3052, Australia.ORCID 0000-0001-6624-4698
Karla HuttOvarian Biology Laboratory, Biomedicine Discovery Institute, Monash University, Melbourne 3800, Australia; karla.hutt@monash.edu.
Australian Regenerative Medicine Institute · AURoyal Women's Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Female fertility and offspring health are critically dependent on an adequate supply of high-quality oocytes, the majority of which are maintained in the ovaries in a unique state of meiotic prophase arrest. While mechanisms of DNA repair during meiotic recombination are well characterized, the same is not true for prophase-arrested oocytes. Here we show that prophase-arrested oocytes rapidly respond to γ-irradiation-induced DNA double-strand breaks by activating Ataxia Telangiectasia Mutated, phosphorylating histone H2AX, and localizing RAD51 to the sites of DNA damage. Despite mobilizing the DNA repair response, even very low levels of DNA damage result in the apoptosis of prophase-arrested oocytes. However, we show that, when apoptosis is inhibited, severe DNA damage is corrected via homologous recombination repair. The repair is sufficient to support fertility and maintain health and genetic fidelity in offspring. Thus, despite the preferential induction of apoptosis following exogenously induced genotoxic stress, prophase-arrested oocytes are highly capable of functionally efficient DNA repair. These data implicate DNA repair as a key quality control mechanism in the female germ line and a critical determinant of fertility and genetic integrity.

Indexed as

DNA Breaks, Double-StrandedAnimalsApoptosisDNA RepairFemaleFertilityMaleMice, Inbred C57BLOocytesProphaseapoptosisDNA damageDNA repairfertilityoocytes

Identifiers

PMID32381741
PMCPMC7260990
OpenAlexW3022807397

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.