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Grant: Discovery Grants Program - Individual

Wilfrid Laurier University

$28,000.00

Figuring out genetic functional systems in Prokaryotes through computational genomics and metagenomics

EF 2016-17

Résumé
The proposed research program is concerned to two problems: (1) Since prokaryotic genomes within a species show high variability in gene content, and since such gene differences can make the difference between a harmless bacterial strain and a pathogenic one, we aim at understanding how different gene sets incorporate into the functional network of their host genome. To this end, we will examine high-quality computationally predicted associations by comparing against knowledge databases and literature, and by finding patterns revealing points of insertion into functional networks. We will concentrate on the role of transcription factors in the integration of genomic islands to their hosts. (2) Since we have developed powerful computational tools for predicting functional interactions in prokaryotic genomes, and there is an increasing abundance of semi-finished genomes, and metagenomic sequences, we aim at expanding these tools towards predicting such interactions with the same quality in any sequences, as when using complete genomes. These predictions will associate unknown genes to well understood functions and provide hints for their later characterization in the laboratory. The proposed work will benefit Canada and the world by providing instruments for finding different versions of gene modules attaining similar functions, from pathogenicity to functions of interest to industry such as cellulose degradation. Such information might help finding new ways for combating disease, or point to novel genes for biotechnological applications.
Programme
Discovery Grants Program - Individual
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
312480-2012
Name nom
MorenoHagelsieb, Gabriel
Department département
Biology
Organization id
35
Institution établissement
Wilfrid Laurier University
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2016
Competition year année de concours
2012
Award amount
28000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
405
Area of application group en
Environment
Area of application group fr
Environnement
Area of application en
Modelling and mathematical simulation of natural processes
Area of application fr
Modélisation et simulation mathématique des processus naturels
Research subject code
5004
Research subject group en
Genetics
Research subject group fr
Génétique
Research subject en
Genome analysis
Research subject fr
Analyse du génome
Partie
5
Nb partie
5
Application title
Figuring out genetic functional systems in Prokaryotes through computational genomics and metagenomics
Keyword
NSERC
Application summary
The proposed research program is concerned to two problems: (1) Since prokaryotic genomes within a species show high variability in gene content, and since such gene differences can make the difference between a harmless bacterial strain and a pathogenic one, we aim at understanding how different gene sets incorporate into the functional network of their host genome. To this end, we will examine high-quality computationally predicted associations by comparing against knowledge databases and literature, and by finding patterns revealing points of insertion into functional networks. We will concentrate on the role of transcription factors in the integration of genomic islands to their hosts. (2) Since we have developed powerful computational tools for predicting functional interactions in prokaryotic genomes, and there is an increasing abundance of semi-finished genomes, and metagenomic sequences, we aim at expanding these tools towards predicting such interactions with the same quality in any sequences, as when using complete genomes. These predictions will associate unknown genes to well understood functions and provide hints for their later characterization in the laboratory. The proposed work will benefit Canada and the world by providing instruments for finding different versions of gene modules attaining similar functions, from pathogenicity to functions of interest to industry such as cellulose degradation. Such information might help finding new ways for combating disease, or point to novel genes for biotechnological applications.