Grant: Canada Research Chairs
Université de Sherbrooke
$200,000.00
Bioinformatics of Non-Coding RNA
FY 2024-25
Summary
Sequencing of whole genomes represented an unprecedented step in the understanding of an organism’s molecular identity. Unexpectedly, over the past two decades, the scientific community discovered that in mammals, non-coding genes are much more numerous than anticipated. The finality of non-coding genes is not to encode proteins, as is the case for most well characterized genes, but rather to produce RNAs that play regulatory roles in their RNA form. However, the set of non-coding genes is still being discovered and functionally characterized. Importantly, we now know that just as changes in the regulation of coding genes can cause disease, the same is true for non-coding genes. The objective of the Canada Research Chair in Bioinformatics of Non-coding RNA is to better understand the contribution of non-coding RNAs to cell function in health and disease. To reach that goal, three main projects will be developed:
1) Large-scale annotation of non-coding genes and cross-species comparison. Non-coding RNAs can be difficult to study using standard tools due to their complex folded structures, multiple copies in genomes and overlap with other genes. To improve genomic annotations, my group will produce large-scale sequencing datasets and computational tools adapted to these features, applying them first in human and then in other species.
2) Functional analysis of small nucleolar RNAs (snoRNAs). Recent years have provided strong evidence of diverse roles in gene expression regulation for a small number of snoRNAs. My group will study this class of non-coding RNAs in a large-scale manner through the integration of diverse sequencing datasets, using bioinformatics and machine learning approaches across different species.
3) Large-scale profiling of RNAs under disease states. The consideration of all RNAs including diverse non-coding RNAs has the potential to open many new doors for the understanding, early detection and treatment of diseases. Through several collaborations, we are using our expertise in non-coding RNA bioinformatics to profile RNAs in pathologies including ovarian cancer, glioblastoma and rheumatoid arthritis.
At the intersection of molecular, health and computer sciences, this research program will considerably improve non-coding RNA understanding across species, enabling their evolutionary, regulatory and functional analysis. This in turn will provide a clearer picture of their cellular roles in health and disease.
Program
Canada Research Chairs
Recipient
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
CRC-2022-00039
Name nom
Scott, Michelle
Department département
Biochemistry and Functional Genomics - Université de Sherbrooke
Organization id
68
Institution établissement
Université de Sherbrooke
Province en
Québec
Province fr
Québec
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2024
Competition year année de concours
2022
Award amount
200000
Program id
CRC
Program name en
Canada Research Chairs
Program name fr
Chaires de recherche du Canada
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
9998
Committee name en
Canada Research Chair Selection Committee
Committee name fr
Comité de sélection des Chaires de recherche du Canada
Area of application code
9999
Area of application group en
Not available
Area of application group fr
Non disponible
Area of application en
Not available
Area of application fr
Non disponible
Research subject code
9999
Research subject group en
Not available
Research subject group fr
Non disponible
Research subject en
Not available
Research subject fr
Non disponible
Field of research list codes
RDF1060504
Field of research list names en
Ethology and sociobiology
Field of research list names fr
Éthologie et sociobiologie
Socioeconomic objective list codes
RDS10704
Socioeconomic objective list names en
Specific population health
Socioeconomic objective list names fr
Santé de populations précises
Application title
Bioinformatics of Non-Coding RNA
Keywords
small nucleolar RNAs (snoRNAs); transcriptomics; gene expression regulation; RNA-RNA interactions; machine learning; reproducibility; genomic annotations; RNA-protein interactions; disease biomarkers; gene evolution
Application summary
Sequencing of whole genomes represented an unprecedented step in the understanding of an organism’s molecular identity. Unexpectedly, over the past two decades, the scientific community discovered that in mammals, non-coding genes are much more numerous than anticipated. The finality of non-coding genes is not to encode proteins, as is the case for most well characterized genes, but rather to produce RNAs that play regulatory roles in their RNA form. However, the set of non-coding genes is still being discovered and functionally characterized. Importantly, we now know that just as changes in the regulation of coding genes can cause disease, the same is true for non-coding genes. The objective of the Canada Research Chair in Bioinformatics of Non-coding RNA is to better understand the contribution of non-coding RNAs to cell function in health and disease. To reach that goal, three main projects will be developed:
1) Large-scale annotation of non-coding genes and cross-species comparison. Non-coding RNAs can be difficult to study using standard tools due to their complex folded structures, multiple copies in genomes and overlap with other genes. To improve genomic annotations, my group will produce large-scale sequencing datasets and computational tools adapted to these features, applying them first in human and then in other species.
2) Functional analysis of small nucleolar RNAs (snoRNAs). Recent years have provided strong evidence of diverse roles in gene expression regulation for a small number of snoRNAs. My group will study this class of non-coding RNAs in a large-scale manner through the integration of diverse sequencing datasets, using bioinformatics and machine learning approaches across different species.
3) Large-scale profiling of RNAs under disease states. The consideration of all RNAs including diverse non-coding RNAs has the potential to open many new doors for the understanding, early detection and treatment of diseases. Through several collaborations, we are using our expertise in non-coding RNA bioinformatics to profile RNAs in pathologies including ovarian cancer, glioblastoma and rheumatoid arthritis.
At the intersection of molecular, health and computer sciences, this research program will considerably improve non-coding RNA understanding across species, enabling their evolutionary, regulatory and functional analysis. This in turn will provide a clearer picture of their cellular roles in health and disease.