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Grant: Discovery Grants Program - Individual

University of Regina

$32,000.00

How the dynamics of DNA shape control bacterial gene expression

EF 2017-18

Résumé
DNA contains the genes that are the blueprints for all living things. Less well known is that DNA does more than store information: it also plays an active role in deciding when to express the information it carries. This control of gene expression occurs through the 3-dimensional shaping and bending of DNA. Our lab studies how bacteria use the dynamic shaping of DNA to respond to changes in their environment. In other words, we research the molecular mechanisms that allow bacteria to perceive, interpret, and then respond to their surroundings. Understanding these mechanisms is critical for determining why some ""good"" bacteria suddenly turn ""bad"" and cause infection, how antibiotic resistance and pathogenicity genes function in different species, and how gene networks can be engineered in bacteria for bioremediation and industrial applications.In this grant we will study the molecular mechanisms by which proteins recognize and bind their DNA targets, how DNA shape influences these interactions, and, conversely, how protein binding modifies DNA shape. We will study the model bacteria Haemophilus influenzae, Escherichia coli, and Salmonella enterica because of the powerful genetic tools available for manipulating these organisms in the lab. This work will employ cutting-edge genomics techniques for visualizing protein and DNA function on a genome-wide scale, as well as molecular biology techniques for characterizing protein-DNA interactions. This research has far-reaching implications because the fundamental molecular mechanisms we study operate in all organisms.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Saskatchewan, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
435784-2013
Name nom
Cameron, Andrew
Department département
Biology
Organization id
17
Institution établissement
University of Regina
Province en
Saskatchewan
Province fr
Saskatchewan
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2017
Competition year année de concours
2013
Award amount
32000
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
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
Research subject code
5200
Research subject group en
Microbiology
Research subject group fr
Microbiologie
Research subject en
Microbiology
Research subject fr
Microbiologie
Partie
5
Nb partie
6
Application title
How the dynamics of DNA shape control bacterial gene expression
Keyword
NSERC
Application summary
DNA contains the genes that are the blueprints for all living things. Less well known is that DNA does more than store information: it also plays an active role in deciding when to express the information it carries. This control of gene expression occurs through the 3-dimensional shaping and bending of DNA. Our lab studies how bacteria use the dynamic shaping of DNA to respond to changes in their environment. In other words, we research the molecular mechanisms that allow bacteria to perceive, interpret, and then respond to their surroundings. Understanding these mechanisms is critical for determining why some ""good"" bacteria suddenly turn ""bad"" and cause infection, how antibiotic resistance and pathogenicity genes function in different species, and how gene networks can be engineered in bacteria for bioremediation and industrial applications.In this grant we will study the molecular mechanisms by which proteins recognize and bind their DNA targets, how DNA shape influences these interactions, and, conversely, how protein binding modifies DNA shape. We will study the model bacteria Haemophilus influenzae, Escherichia coli, and Salmonella enterica because of the powerful genetic tools available for manipulating these organisms in the lab. This work will employ cutting-edge genomics techniques for visualizing protein and DNA function on a genome-wide scale, as well as molecular biology techniques for characterizing protein-DNA interactions. This research has far-reaching implications because the fundamental molecular mechanisms we study operate in all organisms.