Evidence map›Paper›PMID 40018873›Full record

ArticleThe plant genome2025

A pangenome reveals LTR repeat dynamics as a major driver of genome evolution in Chenopodium.

Kate E Jaggi, Karol Krak, Helena Štorchová, Bohumil Mandák, Ashley Marcheschi, Alexander Belyayev, Eric N Jellen, John Sproul, David Jarvis, Peter J Maughan

Abstract read
In one paragraph

Article in The plant genome, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Chromosome-level genome assembly of the AustralianFrontiers in plant science · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

10 authors.

Kate E JaggiDepartment of Plant and Wildlife Sciences, Brigham Young University, Provo, Utah, USA.
Karol KrakInstitute of Botany of the Czech Academy of Sciences, Průhonice, Czech Republic.
Helena ŠtorchováInstitute of Experimental Botany, Czech Academy of Sciences, Prague, Czech Republic.
Bohumil MandákInstitute of Botany of the Czech Academy of Sciences, Průhonice, Czech Republic.
Ashley MarcheschiDepartment of Plant and Wildlife Sciences, Brigham Young University, Provo, Utah, USA.
Alexander BelyayevInstitute of Botany of the Czech Academy of Sciences, Průhonice, Czech Republic.
Eric N JellenDepartment of Plant and Wildlife Sciences, Brigham Young University, Provo, Utah, USA.ORCID https://orcid.org/0000-0002-7906-4845
John SproulDepartment of Biology, Brigham Young University, Provo, Utah, USA.
David JarvisDepartment of Plant and Wildlife Sciences, Brigham Young University, Provo, Utah, USA.
Peter J MaughanDepartment of Plant and Wildlife Sciences, Brigham Young University, Provo, Utah, USA.ORCID https://orcid.org/0000-0003-3714-3411

Funding

Czech Science Foundation 20-20286SCzech Science Foundation RVO67985939National Institute of Food and Agriculture 1022158TowArds Next 997 GENeration Crops CZ.02.01.01/00/22_008/0004581
6 · The paper itself

Abstract

The genus Chenopodium L. is characterized by its wide geographic distribution and ecological adaptability. Species such as quinoa (Chenopodium quinoa Willd.) have served as domesticated staple crops for centuries. Wild Chenopodium species exhibit diverse niche adaptations and are important genetic reservoirs for beneficial agronomic traits, including disease resistance and climate hardiness. To harness the potential of the wild taxa for crop improvement, we developed a Chenopodium pangenome through the assembly and comparative analyses of 12 Chenopodium species that encompass the eight known genome types (A-H). Six of the species are new chromosome-scale assemblies, and many are polyploids; thus, a total of 20 genomes were included in the pangenome analyses. We show that the genomes vary dramatically in size with the D genome being the smallest (∼370 Mb) and the B genome being the largest (∼700 Mb) and that genome size was correlated with independent expansions of the Copia and Gypsy LTR retrotransposon families, suggesting that transposable elements have played a critical role in the evolution of the Chenopodium genomes. We annotated a total of 33,457 pan-Chenopodium gene families, of which ∼65% were classified as shell (2% private). Phylogenetic analysis clarified the evolutionary relationships among the genome lineages, notably resolving the taxonomic placement of the F genome while highlighting the uniqueness of the A genome in the Western Hemisphere. These genomic resources are particularly important for understanding the secondary and tertiary gene pools available for the improvement of the domesticated chenopods while furthering our understanding of the evolution and complexity within the genus.

Indexed as

ChenopodiumEvolution, MolecularGenome, PlantTerminal Repeat SequencesGenome SizePhylogenyRetroelementsRetroelements

Identifiers

PMID40018873
PMCPMC11869160

What OpenQuestion holds

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Registered trials

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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.