Evidence map›Paper›PMID 23071443›Full record

ArticlePLoS genetics2012

The many landscapes of recombination in Drosophila melanogaster.

Josep M Comeron, Ramesh Ratnappan, Samuel Bailin

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 345 papers.

0numbers the graph read from it
0cells of the map it votes in
345citing papers in PubMed
20.9field-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

345 citing papers in PubMed, 596 citations in OpenAlex.

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  11. OutbredbioRxiv : the preprint server for biology · 2026
    Article
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  16. Why recombination hotspots?PLoS genetics · 2026
    Review
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  20. Article

285 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Josep M ComeronDepartment of Biology, University of Iowa, Iowa City, Iowa, USA. josep-comeron@uiowa.edu
Ramesh Ratnappan
Samuel Bailin
University of Iowa · US

Funding

Fine-scale recombination rate variation within and between Drosophila speciesRC2GM092501 · NIGMS · UNIVERSITY OF IOWA · PI COMERON, JOSEP M, JONES, CORBIN D · 2009 to 2010
$1.8M
NIGMS NIH HHS RC2 GM092501NIGMS NIH HHS RC2GM092501
6 · The paper itself

Abstract

Recombination is a fundamental biological process with profound evolutionary implications. Theory predicts that recombination increases the effectiveness of selection in natural populations. Yet, direct tests of this prediction have been restricted to qualitative trends due to the lack of detailed characterization of recombination rate variation across genomes and within species. The use of imprecise recombination rates can also skew population genetic analyses designed to assess the presence and mode of selection across genomes. Here we report the first integrated high-resolution description of genomic and population variation in recombination, which also distinguishes between the two outcomes of meiotic recombination: crossing over (CO) and gene conversion (GC). We characterized the products of 5,860 female meioses in Drosophila melanogaster by genotyping a total of 139 million informative SNPs and mapped 106,964 recombination events at a resolution down to 2 kilobases. This approach allowed us to generate whole-genome CO and GC maps as well as a detailed description of variation in recombination among individuals of this species. We describe many levels of variation in recombination rates. At a large-scale (100 kb), CO rates exhibit extreme and highly punctuated variation along chromosomes, with hot and coldspots. We also show extensive intra-specific variation in CO landscapes that is associated with hotspots at low frequency in our sample. GC rates are more uniformly distributed across the genome than CO rates and detectable in regions with reduced or absent CO. At a local scale, recombination events are associated with numerous sequence motifs and tend to occur within transcript regions, thus suggesting that chromatin accessibility favors double-strand breaks. All these non-independent layers of variation in recombination across genomes and among individuals need to be taken into account in order to obtain relevant estimates of recombination rates, and should be included in a new generation of population genetic models of the interaction between selection and linkage.

Indexed as

Recombination, GeneticAnimalsBase SequenceChromosomesCrossing Over, GeneticDrosophila melanogasterEvolution, MolecularFemaleGene ConversionGenomeMaleNucleotide MotifsPolymorphism, Genetic

Identifiers

PMID23071443
PMCPMC3469467
OpenAlexW1964558095

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.