Evidence map›Paper›PMID 27072809›Full record

ArticleMolecular ecology2016

Rapid genome-wide evolution in Brassica rapa populations following drought revealed by sequencing of ancestral and descendant gene pools.

Steven J Franks, Nolan C Kane, Niamh B O'Hara, Silas Tittes, Joshua S Rest

Abstract read
In one paragraph

Article in Molecular ecology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
–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

37 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
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  7. Article
  8. Climate change and plant genomic plasticity.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2025
    Review
  9. Review
  10. Article
  11. Adaptive radiation of theEcology and evolution · 2024
    Article
  12. Review
  13. Article
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  15. Review
  16. Article
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  18. Vegetable biology and breeding in the genomics era.Science China. Life sciences · 2023
    Review
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  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Steven J FranksDepartment of Biological Sciences, Fordham University, 441 E. Fordham Road, Bronx, NY, 10458, USA.
Nolan C KaneDepartment of Ecology and Evolution, The University of Colorado at Boulder, Ramaley N122, Boulder, CO, 80309, USA.
Niamh B O'HaraDepartment of Biological Sciences, Fordham University, 441 E. Fordham Road, Bronx, NY, 10458, USA.
Silas TittesDepartment of Ecology and Evolution, The University of Colorado at Boulder, Ramaley N122, Boulder, CO, 80309, USA.
Joshua S RestDepartment of Ecology and Evolution, Stony Brook University, 650 Life Sciences, Stony Brook, NY, 11794, USA.

Funding

Fitness and Modularity of Stochastic Variation in Protein Expression LevelsR01GM108904 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI REST, JOSHUA · 2014 to 2018
$927k
NIGMS NIH HHS R01 GM108904
6 · The paper itself

Abstract

There is increasing evidence that evolution can occur rapidly in response to selection. Recent advances in sequencing suggest the possibility of documenting genetic changes as they occur in populations, thus uncovering the genetic basis of evolution, particularly if samples are available from both before and after selection. Here, we had a unique opportunity to directly assess genetic changes in natural populations following an evolutionary response to a fluctuation in climate. We analysed genome-wide differences between ancestors and descendants of natural populations of Brassica rapa plants from two locations that rapidly evolved changes in multiple phenotypic traits, including flowering time, following a multiyear late-season drought in California. These ancestor-descendant comparisons revealed evolutionary shifts in allele frequencies in many genes. Some genes showing evolutionary shifts have functions related to drought stress and flowering time, consistent with an adaptive response to selection. Loci differentiated between ancestors and descendants (FST outliers) were generally different from those showing signatures of selection based on site frequency spectrum analysis (Tajima's D), indicating that the loci that evolved in response to the recent drought and those under historical selection were generally distinct. Very few genes showed similar evolutionary responses between two geographically distinct populations, suggesting independent genetic trajectories of evolution yielding parallel phenotypic changes. The results show that selection can result in rapid genome-wide evolutionary shifts in allele frequencies in natural populations, and highlight the usefulness of combining resurrection experiments in natural populations with genomics for studying the genetic basis of adaptive evolution.

Indexed as

DroughtsEvolution, MolecularGene PoolSelection, GeneticAdaptation, PhysiologicalBrassica rapaCaliforniaGene FrequencyGenetics, PopulationGenome, PlantadaptationBrassica rapaclimate changecontemporary evolutionnatural selectionpopulation genomicsrapid evolution

Identifiers

PMID27072809
PMCPMC4963267

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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.