Grant: Discovery Grants Program - Individual
University of New Brunswick
$41,000.00
Functional analysis of gene duplications
FY 2011-12
Summary
The completion of the human genome sequence has provided us with a wealth of data about the number, types, and organization of the genes required to encode a human. Functional analysis of the genomes of other organisms, such as the fruit fly Drosophila melanogaster and the worm Caenorhabditis elegans, is also being done to try to make sense of the human genome. Comparisons of these different genomes will also help us to determine how genomes of all organisms evolved.
Current theories of genome evolution include the concept that new genes arise by a process of gene duplication. Gene duplication can occur by different processes, including doubling of the whole genome, duplication of a part of a chromosome, or copying of a single gene. Once a gene is duplicated, one of the copies can be inactivated or, in rare cases, it can acquire a new function by a change in its DNA, or mutation. It is thought new functions of duplicated genes are an important force in the diversification of life. Another source of genetic diversity comes from virus-like sequences, called retrotransposons, found in our genome and those of other organisms. These sequences copy themselves and insert into other sites of the genome. However, they can also make copies of gene products which insert into new sites. This type of gene duplication is called retroduplication. The patterns of their evolution and the mechanism of their production aren't yet well defined.
Now that we have several genome sequences in hand, we can ask 1) what parts of retroduplicated genes changed by mutation? 2) do retroduplicated genes have the same or different functions? 3) if a retroduplicated gene acquires mutations that knock out its original function, can it have a new function? 4) what are the mechanisms for retroduplication? This research program will address these questions using the Drosophila genome and genes from other insect species. Computer analysis of gene sequences and the tools of genetics and molecular biology will be used to answer these questions. The answers will help us to understand the process of how genes diversify in function and its significance for organismal evolution.
Program
Discovery Grants Program - Individual
Recipient
Location
New Brunswick, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
171277-2009
Name nom
Clark, Denise
Department département
Biology (Fredericton)
Organization id
75
Institution établissement
University of New Brunswick
Province en
New Brunswick
Province fr
Nouveau-Brunswick
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2011
Competition year année de concours
2009
Award amount
41000
Program id
RGPIN
Program nane 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
33
Committee name en
Molec. & Develop. Genetics
Committee name fr
Gén. moléculaire et dévelop.
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
5002
Research subject group en
Genetics
Research subject group fr
Génétique
Research subject en
Molecular genetics
Research subject fr
Génétique moléculaire
Partie
3
Nb partie
5
Application title
Functional analysis of gene duplications
Keyword
NSERC
Application summary
The completion of the human genome sequence has provided us with a wealth of data about the number, types, and organization of the genes required to encode a human. Functional analysis of the genomes of other organisms, such as the fruit fly Drosophila melanogaster and the worm Caenorhabditis elegans, is also being done to try to make sense of the human genome. Comparisons of these different genomes will also help us to determine how genomes of all organisms evolved.
Current theories of genome evolution include the concept that new genes arise by a process of gene duplication. Gene duplication can occur by different processes, including doubling of the whole genome, duplication of a part of a chromosome, or copying of a single gene. Once a gene is duplicated, one of the copies can be inactivated or, in rare cases, it can acquire a new function by a change in its DNA, or mutation. It is thought new functions of duplicated genes are an important force in the diversification of life. Another source of genetic diversity comes from virus-like sequences, called retrotransposons, found in our genome and those of other organisms. These sequences copy themselves and insert into other sites of the genome. However, they can also make copies of gene products which insert into new sites. This type of gene duplication is called retroduplication. The patterns of their evolution and the mechanism of their production aren't yet well defined.
Now that we have several genome sequences in hand, we can ask 1) what parts of retroduplicated genes changed by mutation? 2) do retroduplicated genes have the same or different functions? 3) if a retroduplicated gene acquires mutations that knock out its original function, can it have a new function? 4) what are the mechanisms for retroduplication? This research program will address these questions using the Drosophila genome and genes from other insect species. Computer analysis of gene sequences and the tools of genetics and molecular biology will be used to answer these questions. The answers will help us to understand the process of how genes diversify in function and its significance for organismal evolution.