Evidence map›Paper›PMID 38124484›Full record

ArticleG3 (Bethesda, Md.)2024

Deleterious phenotypes in wild Arabidopsis arenosa populations are common and linked to runs of homozygosity.

A Cristina Barragan, Maximilian Collenberg, Rebecca Schwab, Sonja Kersten, Merijn H L Kerstens, Doubravka Požárová, Ilja Bezrukov, Felix Bemm, Filip Kolár, Detlef Weigel

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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  3. Biology · 2025
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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

10 authors.

A Cristina BarraganDepartment of Molecular Biology, Max Planck Institute for Biology, 72076 Tübingen, Germany.ORCID 0000-0003-1656-9261
Maximilian CollenbergDepartment of Molecular Biology, Max Planck Institute for Biology, 72076 Tübingen, Germany.
Rebecca SchwabDepartment of Molecular Biology, Max Planck Institute for Biology, 72076 Tübingen, Germany.
Sonja KerstenDepartment of Molecular Biology, Max Planck Institute for Biology, 72076 Tübingen, Germany.
Merijn H L KerstensDepartment of Molecular Biology, Max Planck Institute for Biology, 72076 Tübingen, Germany.ORCID 0000-0003-4131-1721
Doubravka PožárováDepartment of Botany, Faculty of Science, Charles University, 128 01 Prague, Czech Republic.
Ilja BezrukovDepartment of Molecular Biology, Max Planck Institute for Biology, 72076 Tübingen, Germany.
Felix BemmDepartment of Molecular Biology, Max Planck Institute for Biology, 72076 Tübingen, Germany.
Filip KolárDepartment of Botany, Faculty of Science, Charles University, 128 01 Prague, Czech Republic.
Detlef WeigelDepartment of Molecular Biology, Max Planck Institute for Biology, 72076 Tübingen, Germany.ORCID 0000-0002-2114-7963

Funding

Collaborative Research Center 1101 CRC1101Czech Science Foundation 20-22783SDeutsche ForschungsgemeinschaftERC Advanced Grant IMMUNEMESIS 340602Max Planck Society
6 · The paper itself

Abstract

In this study, we aimed to systematically assess the frequency at which potentially deleterious phenotypes appear in natural populations of the outcrossing model plant Arabidopsis arenosa, and to establish their underlying genetics. For this purpose, we collected seeds from wild A. arenosa populations and screened over 2,500 plants for unusual phenotypes in the greenhouse. We repeatedly found plants with obvious phenotypic defects, such as small stature and necrotic or chlorotic leaves, among first-generation progeny of wild A. arenosa plants. Such abnormal plants were present in about 10% of maternal sibships, with multiple plants with similar phenotypes in each of these sibships, pointing to a genetic basis of the observed defects. A combination of transcriptome profiling, linkage mapping and genome-wide runs of homozygosity patterns using a newly assembled reference genome indicated a range of underlying genetic architectures associated with phenotypic abnormalities. This included evidence for homozygosity of certain genomic regions, consistent with alleles that are identical by descent being responsible for these defects. Our observations suggest that deleterious alleles with different genetic architectures are segregating at appreciable frequencies in wild A. arenosa populations.

Indexed as

ArabidopsisChromosome MappingPhenotypeSeedsabnormal phenotypesArabidopsis arenosareference genomeruns of homozygositywild populations

Identifiers

PMID38124484
PMCPMC10917499

What Socratic holds

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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 Socratic graph.