Evidence map›Paper›PMID 18430927›Full record

ArticleGenetics2008

Distinct functions of MLH3 at recombination hot spots in the mouse.

Anton Svetlanov, Frederic Baudat, Paula E Cohen, Bernard de Massy

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

43 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
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  6. HEIP1 orchestrates pro-crossover protein activity during mammalian meiosis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
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  9. Article
  10. Article
  11. Article
  12. Article
  13. Cell genomics · 2023
    Article
  14. Article
  15. Article
  16. Failure to recombine is a common feature of human oogenesis.American journal of human genetics · 2021
    Article
  17. Meiotic Crossover Patterning.Frontiers in cell and developmental biology · 2021
    Review
  18. Article
  19. Article
  20. 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

4 authors at 2 institutions in 2 countries.

Anton SvetlanovDepartment of Biomedical Sciences, Cornell University, Ithaca, New York 14850, USA.
Frederic Baudat
Paula E Cohen
Bernard de Massy
Cornell University · USInstitut de Génétique Humaine · FR

Funding

The MLH1-MLH3 Heterodimer in Mammalian Meiotic Recombination and GameogenesisR01HD041012 · NICHD · YESHIVA UNIVERSITY · PI Paula Elaine Cohen · 2003 to 2026
$7.9M
The MLH1-MLH3 Heterodimer in Mammalian Meiotic Recombination and GametogenesisR56HD041012 · NICHD · CORNELL UNIVERSITY · PI COHEN, PAULA ELAINE · 2008 to 2008
$322k
NICHD NIH HHS HD41012NICHD NIH HHS R01 HD041012NICHD NIH HHS R56 HD041012
6 · The paper itself

Abstract

The four mammalian MutL homologs (MLH1, MLH3, PMS1, and PMS2) participate in a variety of events, including postreplicative DNA repair, prevention of homeologous recombination, and crossover formation during meiosis. In this latter role, MLH1-MLH3 heterodimers predominate and are essential for prophase I progression. Previous studies demonstrated that mice lacking Mlh1 exhibit a 90% reduction in crossing over at the Psmb9 hot spot while noncrossovers, which do not result in exchange of flanking markers but arise from the same double-strand break event, are unaffected. Using a PCR-based strategy that allows for detailed analysis of crossovers and noncrossovers, we show here that Mlh3(-/-) exhibit a 85-94% reduction in the number of crossovers at the Psmb9 hot spot. Most of the remaining crossovers in Mlh3(-/-) meiocytes represent simple exchanges similar to those seen in wild-type mice, with a small fraction (6%) representing complex events that can extend far from the initiation zone. Interestingly, we detect an increase of noncrossovers in Mlh3(-/-) spermatocytes. These results suggest that MLH3 functions predominantly with MLH1 to promote crossovers, while noncrossover events do not require these activities. Furthermore, these results indicate that approximately 10% of crossovers in the mouse are independent of MLH3, suggesting the existence of alternative crossover pathways in mammals.

Indexed as

AnimalsCarrier ProteinsChromosome MappingCrossing Over, GeneticFemaleMiceMutL ProteinsOogenesisOvaryRecombination, GeneticSpermatogenesisCarrier ProteinsMlh3 protein, mouseMutL Proteins

Identifiers

PMID18430927
PMCPMC2323788
OpenAlexW1968215412

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.