Evidence map›Paper›PMID 25888139›Full record

ArticleBMC evolutionary biology2015

A Boolean gene regulatory model of heterosis and speciation.

Peter Martin Ferdinand Emmrich, Hannah Elizabeth Roberts, Vera Pancaldi

Abstract read
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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 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Peter Martin Ferdinand EmmrichDepartment of Plant Sciences, University of Cambridge, CB2 3EA, Cambridge, UK. peter.emmrich@jic.ac.uk.
Hannah Elizabeth RobertsDepartment of Plant Sciences, University of Cambridge, CB2 3EA, Cambridge, UK. h.roberts283@gmail.com.
Vera PancaldiDepartment of Plant Sciences, University of Cambridge, CB2 3EA, Cambridge, UK. vpancaldi@cnio.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundModelling genetic phenomena affecting biological traits is important for the development of agriculture as it allows breeders to predict the potential of breeding for certain traits. One such phenomenon is heterosis or hybrid vigor: crossing individuals from genetically distinct populations often results in improvements in quantitative traits, such as growth rate, biomass production and stress resistance. Heterosis has become a very useful tool in global agriculture, but its genetic basis remains controversial and its effects hard to predict. We have taken a computational approach to studying heterosis, developing a simulation of evolution, independent reassortment of alleles and hybridization of Gene Regulatory Networks (GRNs) in a Boolean framework. These artificial regulatory networks exhibit topological properties that reflect those observed in biology, and fitness is measured as the ability of a network to respond to external inputs in a pre-defined way.

resultsOur model reproduced common experimental observations on heterosis using only biologically justified parameters, such as mutation rates. Hybrid vigor was observed and its extent was seen to increase as parental populations diverged, up until a point of sudden collapse of hybrid fitness. Thus, the model also describes a process akin to speciation due to genetic incompatibility of the separated populations. We also reproduce, for the first time in a model, the fact that hybrid vigor cannot easily be fixed by within a breeding line, currently an important limitation of the use of hybrid crops. The simulation allowed us to study the effects of three standard models for the genetic basis of heterosis: dominance, over-dominance, and epistasis.

conclusionThis study describes the most detailed simulation of heterosis using gene regulatory networks to date and reproduces several phenomena associated with heterosis for the first time in a model. The level of detail in our model allows us to suggest possible warning signs of the impending collapse of hybrid vigor in breeding. In addition, the simulation provides a framework that can be extended to study other aspects of heterosis and alternative evolutionary scenarios.

Indexed as

Gene Regulatory NetworksHybrid VigorModels, GeneticBreedingComputer SimulationCrops, AgriculturalEpistasis, GeneticGenetic FitnessGenetic SpeciationHeterozygoteHybridization, Genetic

Identifiers

PMID25888139
PMCPMC4349475

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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.