Evidence map›Paper›PMID 27838628›Full record

ArticleGenetics2017

Variation and Evolution of the Meiotic Requirement for Crossing Over in Mammals.

Beth L Dumont

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
7.5field-weighted citation impact, top 3% 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

33 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
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  13. Background selection under evolving recombination rates.Proceedings. Biological sciences · 2022
    Article
  14. Review
  15. Article
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  17. Introgression reshapes recombination distribution in grapevine interspecific hybrids.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2019
    Article
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  19. Review
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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

1 author at 1 institution in 1 country.

Beth L DumontInitiative in Biological Complexity, North Carolina State University, Raleigh, North Carolina 27695 beth.dumont@jax.org.
North Carolina State University · US

Funding

Mechanisms of Recurrent, Parallel Loss of X/Y Pairing and Recombination at Meiosis in VolesR00GM110332 · NIGMS · JACKSON LABORATORY · PI DUMONT, BETHANY L · 2017 to 2019
$746k
Mechanisms of Recurrent, Parallel Loss of X/Y Pairing and Recombination at MeiosiK99GM110332 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI DUMONT, BETHANY L · 2014 to 2015
$164k
NIGMS NIH HHS K99 GM110332NIGMS NIH HHS R00 GM110332
6 · The paper itself

Abstract

The segregation of homologous chromosomes at the first meiotic division is dependent on the presence of at least one well-positioned crossover per chromosome. In some mammalian species, however, the genomic distribution of crossovers is consistent with a more stringent baseline requirement of one crossover per chromosome arm. Given that the meiotic requirement for crossing over defines the minimum frequency of recombination necessary for the production of viable gametes, determining the chromosomal scale of this constraint is essential for defining crossover profiles predisposed to aneuploidy and understanding the parameters that shape patterns of recombination rate evolution across species. Here, I use cytogenetic methods for in situ imaging of crossovers in karyotypically diverse house mice (Mus musculus domesticus) and voles (genus Microtus) to test how chromosome number and configuration constrain the distribution of crossovers in a genome. I show that the global distribution of crossovers in house mice is thresholded by a minimum of one crossover per chromosome arm, whereas the crossover landscape in voles is defined by a more relaxed requirement of one crossover per chromosome. I extend these findings in an evolutionary metaanalysis of published recombination and karyotype data for 112 mammalian species and demonstrate that the physical scale of the genomic crossover distribution has undergone multiple independent shifts from one crossover per chromosome arm to one per chromosome during mammalian evolution. Together, these results indicate that the chromosomal scale constraint on crossover rates is itself a trait that evolves among species, a finding that casts light on an important source of crossover rate variation in mammals.

Indexed as

Chromosome SegregationCrossing Over, GeneticAnimalsArvicolinaeBiological EvolutionEvolution, MolecularGenetic VariationGenomeMaleMeiosisMiceMutL Protein Homolog 1Nuclear ProteinsPhylogenyRecombination, GeneticSynaptonemal ComplexMlh1 protein, mouseMutL Protein Homolog 1Nuclear Proteinscrossing overhouse mousekaryotypemeiosisMicrotusMLH1Mus musculusrecombinationRobertsonian translocationvoles

Identifiers

PMID27838628
PMCPMC5223500
OpenAlexW2552473057

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.