Evidence map›Paper›PMID 42365000›Full record

ArticleNature communications2026

Wild tomato genome assemblies reveal structural variants and repeat content act as recombination barriers.

Willem M J van Rengs, Roven Rommel Fuentes, Zahra Zangishei, Elias Primetis, Yazhong Wang, Joiselle B Fernandes, Tamara Susanto, Qichao Lian, Sieglinde Effgen, Bruno Huettel and 3 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Willem M J van Rengs *Department of Chromosome Biology, Max Planck Institute for Plant Breeding Research, Carl-von-Linné-Weg 10, Cologne, Germany.
Roven Rommel Fuentes *Department of Chromosome Biology, Max Planck Institute for Plant Breeding Research, Carl-von-Linné-Weg 10, Cologne, Germany.ORCID 0009-0002-8512-619X
Zahra Zangishei *Faculty of Mathematics and Natural Sciences, Institute of Biological Data Science, CEPLAS, Heinrich Heine University Düsseldorf, Düsseldorf, Germany.ORCID 0000-0003-3882-8164
Elias Primetis *Department of Chromosome Biology, Max Planck Institute for Plant Breeding Research, Carl-von-Linné-Weg 10, Cologne, Germany.ORCID 0000-0003-0502-2447
Yazhong WangDepartment of Chromosome Biology, Max Planck Institute for Plant Breeding Research, Carl-von-Linné-Weg 10, Cologne, Germany.ORCID 0000-0001-8150-7230
Joiselle B FernandesDepartment of Chromosome Biology, Max Planck Institute for Plant Breeding Research, Carl-von-Linné-Weg 10, Cologne, Germany.ORCID 0000-0003-2540-2439
Tamara SusantoDepartment of Chromosome Biology, Max Planck Institute for Plant Breeding Research, Carl-von-Linné-Weg 10, Cologne, Germany.ORCID 0000-0002-4785-1166
Qichao LianDepartment of Chromosome Biology, Max Planck Institute for Plant Breeding Research, Carl-von-Linné-Weg 10, Cologne, Germany.ORCID 0000-0003-0737-8332
Sieglinde EffgenDepartment of Chromosome Biology, Max Planck Institute for Plant Breeding Research, Carl-von-Linné-Weg 10, Cologne, Germany.
Bruno HuettelMax Planck Genome-center, Max Planck Institute for Plant Breeding Research, Carl-von-Linné-Weg 10, Cologne, Germany.ORCID 0000-0001-7165-1714
Saleh AlseekhMax-Planck-Institute of Molecular Plant Physiology, Am Mühlenberg, Potsdam-Golm, Germany.ORCID 0000-0003-2067-5235
Björn UsadelFaculty of Mathematics and Natural Sciences, Institute of Biological Data Science, CEPLAS, Heinrich Heine University Düsseldorf, Düsseldorf, Germany. b.usadel@fz-juelich.de.ORCID 0000-0003-0921-8041
Charles J UnderwoodDepartment of Chromosome Biology, Max Planck Institute for Plant Breeding Research, Carl-von-Linné-Weg 10, Cologne, Germany. cunderwood@mpipz.mpg.de.ORCID 0000-0001-5730-6279

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) 452682775Deutsche Forschungsgemeinschaft (German Research Foundation) 465339501Deutsche Forschungsgemeinschaft (German Research Foundation) EXC 390686111EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 101076355
6 · The paper itself

Abstract

Crop wild relatives are used to improve cultivated plants and precise tracking of genetic introgression requires high-quality genome assemblies. Here we present de novo genome assemblies of two wild tomato species - the broadly stress-resistant Solanum pennellii (LA0716) and the salt-resistant Solanum cheesmaniae (LA1039). The improved S. pennellii genome adds 146 Mbp to the twelve chromosomes compared with the original reference. The alignment of the new assemblies with multiple gold-standard assemblies identified shared and species-specific structural variants. Analysis of repeat content demonstrates independent explosions of Tekay retrotransposons in S. pennellii and S. peruvianum. Genome sequencing of 709 recombinant plants derived from male and female backcrosses of three different hybrids reveals higher crossover rate in female meiosis. Conserved female-enhanced recombination regions were discovered and coldspots were attributed to megabase-scale inversions and insertion-deletion polymorphisms. Our S. pennellii and S. cheesmaniae genome assemblies reveal how repeat content diverged in nature and during breeding, and uncovers how both reproductive gender and structural variants dictate recombination landscapes in tomato hybrids.

Indexed as

Genome, PlantRecombination, GeneticSolanumSolanum lycopersicumChromosomes, PlantRetroelementsRetroelements

Identifiers

PMID42365000
PMCPMC13310191

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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.