Evidence map›Paper›PMID 20837996›Full record

ArticleGenetics2010

Floral genetic architecture: an examination of QTL architecture underlying floral (co)variation across environments.

Marcus T Brock, Jennifer M Dechaine, Federico L Iniguez-Luy, Julin N Maloof, John R Stinchcombe, Cynthia Weinig

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In one paragraph

Article in Genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Article
  2. Plastic responses to novel environments are biased towards phenotype dimensions with high additive genetic variation.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
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  5. Review
  6. Article
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  10. A genetic linkage map of Brassica carinata constructed with a doubled haploid population.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2012
    Article
  11. Article
  12. Article
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  14. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Marcus T BrockDepartment of Botany, University of Wyoming, Laramie, WY 82071, USA. mbrock2@uwyo.edu
Jennifer M Dechaine
Federico L Iniguez-Luy
Julin N Maloof
John R Stinchcombe
Cynthia Weinig

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic correlations are expected to be high among functionally related traits and lower between groups of traits with distinct functions (e.g., reproductive vs. resource-acquisition traits). Here, we explore the quantitative-genetic and QTL architecture of floral organ sizes, vegetative traits, and life history in a set of Brassica rapa recombinant inbred lines within and across field and greenhouse environments. Floral organ lengths were strongly positively correlated within both environments, and analysis of standardized G-matrices indicates that the structure of genetic correlations is ∼80% conserved across environments. Consistent with these correlations, we detected a total of 19 and 21 additive-effect floral QTL in the field and the greenhouse, respectively, and individual QTL typically affected multiple organ types. Interestingly, QTL×QTL epistasis also appeared to contribute to observed genetic correlations; i.e., interactions between two QTL had similar effects on filament length and two estimates of petal size. Although floral and nonfloral traits are hypothesized to be genetically decoupled, correlations between floral organ size and both vegetative and life-history traits were highly significant in the greenhouse; G-matrices of floral and vegetative traits as well as floral and life-history traits differed across environments. Correspondingly, many QTL (45% of those mapped in the greenhouse) showed environmental interactions, including approximately even numbers of floral and nonfloral QTL. Most instances of QTL×QTL epistasis for floral traits were environment dependent.

Indexed as

EnvironmentQuantitative Trait LociEpistasis, GeneticFlowers

Identifiers

PMID20837996
PMCPMC2998323

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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.