Evidence map›Paper›PMID 31513571›Full record

ArticlePLoS genetics2019

Integrating transcriptomic network reconstruction and eQTL analyses reveals mechanistic connections between genomic architecture and Brassica rapa development.

Robert L Baker, Wen Fung Leong, Marcus T Brock, Matthew J Rubin, R J Cody Markelz, Stephen Welch, Julin N Maloof, Cynthia Weinig

Erratum issuedAbstract read
In one paragraph

Article in PLoS genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Robert L BakerDepartment of Biology, Miami University, Oxford, Ohio, United States of America.ORCID 0000-0001-7591-5035
Wen Fung LeongDepartment of Agronomy, Kansas State University, Manhattan, Kansas, United States of America.ORCID 0000-0003-0514-4057
Marcus T BrockDepartment of Botany, University of Wyoming, Laramie, Wyoming, United States of America.
Matthew J RubinDepartment of Botany, University of Wyoming, Laramie, Wyoming, United States of America.ORCID 0000-0001-5484-2324
R J Cody MarkelzDepartment of Plant Biology, University of California Davis, Davis, California, United States of America.
Stephen WelchDepartment of Agronomy, Kansas State University, Manhattan, Kansas, United States of America.
Julin N MaloofDepartment of Plant Biology, University of California Davis, Davis, California, United States of America.ORCID 0000-0002-9623-2599
Cynthia WeinigDepartment of Botany, University of Wyoming, Laramie, Wyoming, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plant developmental dynamics can be heritable, genetically correlated with fitness and yield, and undergo selection. Therefore, characterizing the mechanistic connections between the genetic architecture governing plant development and the resulting ontogenetic dynamics of plants in field settings is critically important for agricultural production and evolutionary ecology. We use hierarchical Bayesian Function-Valued Trait (FVT) models to estimate Brassica rapa growth curves throughout ontogeny, across two treatments, and in two growing seasons. We find genetic variation for plasticity of growth rates and final sizes, but not the inflection point (transition from accelerating to decelerating growth) of growth curves. There are trade-offs between growth rate and duration, indicating that selection for maximum yields at early harvest dates may come at the expense of late harvest yields and vice versa. We generate eigengene modules and determine which are co-expressed with FVT traits using a Weighted Gene Co-expression Analysis. Independently, we seed a Mutual Rank co-expression network model with FVT traits to identify specific genes and gene networks related to FVT. GO-analyses of eigengene modules indicate roles for actin/cytoskeletal genes, herbivore resistance/wounding responses, and cell division, while MR networks demonstrate a close association between metabolic regulation and plant growth. We determine that combining FVT Quantitative Trait Loci (QTL) and MR genes/WGCNA eigengene expression profiles better characterizes phenotypic variation than any single data type (i.e. QTL, gene, or eigengene alone). Our network analysis allows us to employ a targeted eQTL analysis, which we use to identify regulatory hotspots for FVT. We examine cis vs. trans eQTL that mechanistically link FVT QTL with structural trait variation. Colocalization of FVT, gene, and eigengene eQTL provide strong evidence for candidate genes influencing plant height. The study is the first to explore eQTL for FVT, and specifically do so in agroecologically relevant field settings.

Indexed as

Bayes TheoremBrassica rapaGene Expression ProfilingGene Expression Regulation, PlantGene Regulatory NetworksGenomicsGenotypePhenotypeQuantitative Trait LociTranscriptome

Identifiers

PMID31513571
PMCPMC6759183

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LicenceCC BY
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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.