Grant: Discovery Grants Program - Individual
Dalhousie University
$66,000.00
The role of ancient supergenes and genomic structural variation in contemporary intra-specific biodiversity
FY 2023-24
Summary
Understanding individual-based genetic differences within wild populations is central to our understanding of biodiversity, how species form, and successful resource management. Genomic structural variation represents the largest source of inter-individual genetic variation and is defined as genomic regions that differ in copy number, orientation, or chromosomal location. Chromosomal rearrangements can capture suites of co-adapted alleles providing protection from recombination, and a source of modular standing variation facilitating the formation of complex phenotypes. The overarching theme of my research program is to examine the role of chromosomal structural variation in adaptive diversity within widely distributed and often high gene flow aquatic species. The hypothesis being examined is that adaptive differences in aquatic species that are characterized by high dispersal potential are commonly associated with existing and often ancient chromosomal structural variants that protect suits of co-adapted alleles from recombination providing a source of existing modular standing variation. Species identified for inclusion were chosen to represent a wide range of dispersal potential and levels of gene flow, and as such, a long-term goal of this program is to evaluate the association between structure variation, life history as it relates to dispersal potential and gene flow, and the formation of complex phenotypes. Specifically, the main objectives are to: 1) evaluate and develop bioinformatic and statistical solutions for detecting, and analyzing structural variation; 2) identify structural variants across the genomes of a diverse suite of marine taxa and explore their phylogenies; 3) explore associations among chromosomal structural variation and environmental, life history variation, and genome wide gene expression. Comparisons across these taxa will allow an examination of the interplay between gene flow, selection, and structural variation in the formation of complex phenotypes. Potential theoretical and applied outcomes of this work include an improved understanding of how chromosomal re-arrangements may modulate the interplay between selection, drift, and gene flow in marine species, and the identification of phenotypically linked variants or keystone supergenes which may provide unprecedented opportunity for integration into existing management and assessment paradigms.
Program
Discovery Grants Program - Individual
Recipient
Location
Nova Scotia, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
RGPIN-2019-03998
Name nom
Bradbury, Ian
Department département
Biology
Organization id
79
Institution établissement
Dalhousie University
Province en
Nova Scotia
Province fr
Nouvelle-Écosse
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2023
Competition year année de concours
2019
Award amount
66000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1503
Committee name en
Evolution and Ecology
Committee name fr
Évolution et écologie
Area of application code
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
5004
Research subject group en
Genetics
Research subject group fr
Genome analysis
Research subject en
Génétique
Research subject fr
Analyse du génome
Application title
The role of ancient supergenes and genomic structural variation in contemporary intra-specific biodiversity
Keyword
adaptation; Chromosomal rearrangements; genomic structural variation; marine conservation; Population genetics; Population genomics
Application summary
Understanding individual-based genetic differences within wild populations is central to our understanding of biodiversity, how species form, and successful resource management. Genomic structural variation represents the largest source of inter-individual genetic variation and is defined as genomic regions that differ in copy number, orientation, or chromosomal location. Chromosomal rearrangements can capture suites of co-adapted alleles providing protection from recombination, and a source of modular standing variation facilitating the formation of complex phenotypes. The overarching theme of my research program is to examine the role of chromosomal structural variation in adaptive diversity within widely distributed and often high gene flow aquatic species. The hypothesis being examined is that adaptive differences in aquatic species that are characterized by high dispersal potential are commonly associated with existing and often ancient chromosomal structural variants that protect suits of co-adapted alleles from recombination providing a source of existing modular standing variation. Species identified for inclusion were chosen to represent a wide range of dispersal potential and levels of gene flow, and as such, a long-term goal of this program is to evaluate the association between structure variation, life history as it relates to dispersal potential and gene flow, and the formation of complex phenotypes. Specifically, the main objectives are to: 1) evaluate and develop bioinformatic and statistical solutions for detecting, and analyzing structural variation; 2) identify structural variants across the genomes of a diverse suite of marine taxa and explore their phylogenies; 3) explore associations among chromosomal structural variation and environmental, life history variation, and genome wide gene expression. Comparisons across these taxa will allow an examination of the interplay between gene flow, selection, and structural variation in the formation of complex phenotypes. Potential theoretical and applied outcomes of this work include an improved understanding of how chromosomal re-arrangements may modulate the interplay between selection, drift, and gene flow in marine species, and the identification of phenotypically linked variants or keystone supergenes which may provide unprecedented opportunity for integration into existing management and assessment paradigms.