Evidence map›Paper›PMID 25567288›Full record

ArticleScientific reports2015

Meiotic interstrand DNA damage escapes paternal repair and causes chromosomal aberrations in the zygote by maternal misrepair.

Francesco Marchetti, Jack Bishop, John Gingerich, Andrew J Wyrobek

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
16.1field-weighted citation impact, top 1% 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

27 citing papers in PubMed, 66 citations in OpenAlex.

  1. Effects of Cytotoxic Therapies on the Sperm Genome and Epigenome.Advances in experimental medicine and biology · 2026
    Review
  2. Article
  3. Article
  4. Male aging in germ cells: What are we inheriting?Genetics and molecular biology · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. The Effect of Sperm DNA Fragmentation onFrontiers in endocrinology · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Observational
  14. Review
  15. Article
  16. Article
  17. Review
  18. Use of Confocal Microscopy to Evaluate Equine Zygote Development After Sperm Injection of Oocytes Matured In Vivo or In Vitro.Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada · 2017
    Article
  19. Article
  20. 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

4 authors at 3 institutions in 2 countries.

Francesco Marchetti1] Environmental Health Science Research Bureau, Health Canada, Ottawa, Ontario, Canada, K1A 0K9 [2] Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, USA 94720 [3] Biosciences Department, Lawrence Livermore National Laboratory, Livermore, California 94550, USA.
Jack BishopNational Toxicology Program, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA.
John GingerichEnvironmental Health Science Research Bureau, Health Canada, Ottawa, Ontario, Canada, K1A 0K9.
Andrew J Wyrobek1] Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, USA 94720 [2] Biosciences Department, Lawrence Livermore National Laboratory, Livermore, California 94550, USA.
Health Canada · CALawrence Berkeley National Laboratory · USNational Institute of Environmental Health Sciences · US

Funding

NIEHS NIH HHS Y01-ES-102-00
6 · The paper itself

Abstract

De novo point mutations and chromosomal structural aberrations (CSA) detected in offspring of unaffected parents show a preferential paternal origin with higher risk for older fathers. Studies in rodents suggest that heritable mutations transmitted from the father can arise from either paternal or maternal misrepair of damaged paternal DNA, and that the entire spermatogenic cycle can be at risk after mutagenic exposure. Understanding the susceptibility and mechanisms of transmission of paternal mutations is important in family planning after chemotherapy and donor selection for assisted reproduction. We report that treatment of male mice with melphalan (MLP), a bifunctional alkylating agent widely used in chemotherapy, induces DNA lesions during male mouse meiosis that persist unrepaired as germ cells progress through DNA repair-competent phases of spermatogenic development. After fertilization, unrepaired sperm DNA lesions are mis-repaired into CSA by the egg's DNA repair machinery producing chromosomally abnormal offspring. These findings highlight the importance of both pre- and post-fertilization DNA repair in assuring the genomic integrity of the conceptus.

Indexed as

AnimalsChromosome AberrationsDNA DamageDNA RepairMaleMeiosisMelphalanMiceSpermatozoaZygoteMelphalan

Identifiers

PMID25567288
PMCPMC4286742
OpenAlexW1997128871

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.