Evidence map›Paper›PMID 18247060›Full record

ArticleCell and tissue research2008

Completion of meiosis in male zebrafish (Danio rerio) despite lack of DNA mismatch repair gene mlh1.

Marcelo C Leal, Harma Feitsma, Edwin Cuppen, Luiz R França, Rüdiger W Schulz

Open access · hybridAbstract read
In one paragraph

Article in Cell and tissue research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Meiotic Recombination in Teleosts.Advances in experimental medicine and biology · 2026
    Review
  2. Long Non-Coding RNAInternational journal of molecular sciences · 2025
    Article
  3. Direct male development in chromosomally ZZ zebrafish.Frontiers in cell and developmental biology · 2024
    Article
  4. Achiasmatic meiosis in the unisexual Amazon molly, Poecilia formosa.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2022
    Article
  5. Article
  6. Meiotic Chromosome Dynamics in Zebrafish.Frontiers in cell and developmental biology · 2021
    Review
  7. Zebrafish Cancer Predisposition Models.Frontiers in cell and developmental biology · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. brca2 in zebrafish ovarian development, spermatogenesis, and tumorigenesis.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
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 4 institutions in 3 countries.

Marcelo C LealScience Faculty, Department Biology, Section Endocrinology & Metabolism, Utrecht University, Kruyt Building, Room Z-203, Padualaan 8, NL-3584 CH Utrecht, The Netherlands.
Harma Feitsma
Edwin Cuppen
Luiz R França
Rüdiger W Schulz
Hubrecht Institute for Developmental Biology and Stem Cell Research · NLNorwegian Institute of Marine Research · NOUniversidade Federal de Minas Gerais · BRUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mlh1 is a member of DNA mismatch repair (MMR) machinery and is also essential for the stabilization of crossovers during the first meiotic division. Recently, we have shown that zebrafish mlh1 mutant males are completely infertile because of a block in metaphase I, whereas females are fertile but have aneuploid progeny. When studying fertility in males in a two-fold more inbred background, we have however observed low numbers of fertilized eggs (approximately 0.4%). Histological examination of the testis has revealed that all spermatogenic stages prior to spermatids (spermatogonia, primary spermatocytes, and secondary spermatocytes) are significantly increased in the mutant, whereas the total weight of spermatids and spermatozoa is highly decreased (1.8 mg in wild-type vs. 0.1 mg in mutants), a result clearly different from our previous study in which outbred males lack secondary spermatocytes or postmeiotic cells. Thus, a delay of both meiotic divisions occurs rather than complete arrest during meiosis I in these males. Eggs fertilized with mutant sperm develop as malformed embryos and are aneuploid making this male phenotype much more similar to that previously described in the mutant females. Therefore, crossovers are still essential for proper meiosis, but meiotic cell divisions can progress without it, suggesting that this mutant is a suitable model for studying the cellular mechanisms of completing meiosis without crossover stabilization.

Indexed as

DNA Mismatch RepairAdaptor Proteins, Signal TransducingAneuploidyAnimalsAnimals, Genetically ModifiedApoptosisEmbryo, NonmammalianFemaleFertilityHistonesIn Situ Nick-End LabelingMaleMeiosisMutL Protein Homolog 1Nuclear ProteinsOrgan SizeAdaptor Proteins, Signal TransducingHistonesMlh1 protein, zebrafishMutL Protein Homolog 1Nuclear ProteinsZebrafish Proteins

Identifiers

PMID18247060
PMCPMC2668577
OpenAlexW2130395542

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.