Evidence map›Paper›PMID 26049736›Full record

ArticleBMC evolutionary biology2015

Dearth of polymorphism associated with a sustained response to selection for flowering time in maize.

Eleonore Durand, Maud I Tenaillon, Xavier Raffoux, Stéphanie Thépot, Matthieu Falque, Philippe Jamin, Aurélie Bourgais, Adrienne Ressayre, Christine Dillmann

Abstract read
In one paragraph

Article in BMC evolutionary biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

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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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Genomics of Long- and Short-Term Adaptation in Maize and Teosintes.Methods in molecular biology (Clifton, N.J.) · 2020
    Review
  6. Article
  7. Article
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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

9 authors.

Eleonore DurandINRA, Ferme du Moulon, Gif sur Yvette, 91190, France. eleonore.durand@univ-lille1.fr.
Maud I TenaillonCNRS, Ferme du Moulon, Gif sur Yvette, 91190, France. tenaillon@moulon.inra.fr.
Xavier RaffouxINRA, Ferme du Moulon, Gif sur Yvette, 91190, France. raffoux@moulon.inra.fr.
Stéphanie ThépotINRA, Ferme du Moulon, Gif sur Yvette, 91190, France. stephanie.thepot@gmail.com.
Matthieu FalqueINRA, Ferme du Moulon, Gif sur Yvette, 91190, France. falque@moulon.inra.fr.
Philippe JaminINRA, Ferme du Moulon, Gif sur Yvette, 91190, France. jamin@moulon.inra.fr.
Aurélie BourgaisCNRS, Ferme du Moulon, Gif sur Yvette, 91190, France. bourgais@moulon.inra.fr.
Adrienne RessayreINRA, Ferme du Moulon, Gif sur Yvette, 91190, France. ressayre@moulon.inra.fr.
Christine DillmannUniv Paris-Sud, Ferme du Moulon, Gif sur Yvette, 91190, France. dillmann@moulon.inra.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLong term selection experiments bring unique insights on the genetic architecture of quantitative traits and their evolvability. Indeed, they are utilized to (i) monitor changes in allele frequencies and assess the effects of genomic regions involved traits determinism; (ii) evaluate the role of standing variation versus new mutations during adaptation; (iii) investigate the contribution of non allelic interactions. Here we describe genetic and phenotypic evolution of two independent Divergent Selection Experiments (DSEs) for flowering time conducted during 16 years from two early maize inbred lines.

resultsOur experimental design uses selfing as the mating system and small population sizes, so that two independent families evolved within each population, Late and Early. Observed patterns are strikingly similar between the two DSEs. We observed a significant response to selection in both directions during the first 7 generations of selection. Within Early families, the response is linear through 16 generations, consistent with the maintenance of genetic variance. Within Late families and despite maintenance of significant genetic variation across 17 generations, the response to selection reached a plateau after 7 generations. This plateau is likely caused by physiological limits. Residual heterozygosity in the initial inbreds can partly explain the observed responses as evidenced by 42 markers derived from both Methyl-Sensitive Amplification- and Amplified Fragment Length- Polymorphisms. Among the 42, a subset of 13 markers most of which are in high linkage disequilibrium, display a strong association with flowering time variation. Their fast fixation throughout DSEs' pedigrees results in strong genetic differentiation between populations and families.

conclusionsOur results reveal a paradox between the sustainability of the response to selection and the associated dearth of polymorphisms. Among other hypotheses, we discuss the maintenance of heritable variation by few mutations with strong epistatic interactions whose effects are modified by continuous changes of the genetic background through time.

Indexed as

FlowersPolymorphism, GeneticSelection, GeneticBiological EvolutionEpigenesis, GeneticGene FrequencyLinkage DisequilibriumMutationZea mays

Identifiers

PMID26049736
PMCPMC4458035

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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.