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Grant: Discovery Grants Program - Individual

University of Lethbridge

$36,000.00

Structure, function and evolution of small RNAs in unicellular eukaryotes

FY 2018-19

Summary
Ribonucleic acid (RNA) molecules called non-coding RNAs (ncRNAs) have diverse functions, controlling a variety of cellular processes in all organisms. Many eukaryotic genomes contain more genomic DNA sequence specifying the production of ncRNAs than specifying proteins and yet, the detailed function of most of these ncRNAs remains unknown. Consequently, identifying and determining functions of ncRNAs is becoming an increasingly important area of functional genomics - relating genomic DNA sequence to biological function - and is a primary objective of my research program. We will study ncRNAs in the unicellular eukaryotes called protists, organisms that comprise the bulk of eukaryotic evolutionary diversity. Nobel prize-winning discoveries were the result of first characterizing ncRNAs and their cellular functions in protists, such as self-splicing (autocatalytic) introns and telomerase RNA, both first identified in Tetrahymena thermophila. Two main classes of ncRNAs that we will investigate are the small nucleolar (sno) and small nuclear (sn) RNAs. SnoRNAs are known to have a functional role in the synthesis of ribosomes - the complexes responsible for protein synthesis in the cell. We will use an in vivo approach to determine the specific roles of individual snoRNAs during ribosome synthesis in the protist Euglena gracilis, an organism with a particularly complex ribosome assembly pathway. SnRNAs are core components of the eukaryote-specific cellular structure(s) termed the spliceosome. Spliceosomes are required for the removal of intervening sequences (introns) from protein-coding RNAs, a process called splicing. We will characterize splicing and spliceosome components in the early-diverging protist Giardia lamblia. This organism is particularly interesting because it possesses a very unusual splicing system, contains relatively few introns, and appears to be undergoing intron loss as it reduces its genome size and further adapts to its parasitic lifestyle. We will also characterize gene expression pathways and cellular components used for ncRNA synthesis in these protists, and exploit their evolutionary positions to derive insights about ncRNA and spliceosome evolution in eukaryotes.
Program
Discovery Grants Program - Individual
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
355757-2013
Name nom
Russell, Anthony
Department département
Biological Sciences
Organization id
12
Institution établissement
University of Lethbridge
Province en
Alberta
Province fr
Alberta
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2018
Competition year année de concours
2013
Award amount
36000
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
5002
Research subject group en
Genetics
Research subject group fr
Génétique
Research subject en
Molecular genetics
Research subject fr
Génétique moléculaire
Partie
5
Nb partie
5
Application title
Structure, function and evolution of small RNAs in unicellular eukaryotes
Keyword
NSERC
Application summary
Ribonucleic acid (RNA) molecules called non-coding RNAs (ncRNAs) have diverse functions, controlling a variety of cellular processes in all organisms. Many eukaryotic genomes contain more genomic DNA sequence specifying the production of ncRNAs than specifying proteins and yet, the detailed function of most of these ncRNAs remains unknown. Consequently, identifying and determining functions of ncRNAs is becoming an increasingly important area of functional genomics - relating genomic DNA sequence to biological function - and is a primary objective of my research program. We will study ncRNAs in the unicellular eukaryotes called protists, organisms that comprise the bulk of eukaryotic evolutionary diversity. Nobel prize-winning discoveries were the result of first characterizing ncRNAs and their cellular functions in protists, such as self-splicing (autocatalytic) introns and telomerase RNA, both first identified in Tetrahymena thermophila. Two main classes of ncRNAs that we will investigate are the small nucleolar (sno) and small nuclear (sn) RNAs. SnoRNAs are known to have a functional role in the synthesis of ribosomes - the complexes responsible for protein synthesis in the cell. We will use an in vivo approach to determine the specific roles of individual snoRNAs during ribosome synthesis in the protist Euglena gracilis, an organism with a particularly complex ribosome assembly pathway. SnRNAs are core components of the eukaryote-specific cellular structure(s) termed the spliceosome. Spliceosomes are required for the removal of intervening sequences (introns) from protein-coding RNAs, a process called splicing. We will characterize splicing and spliceosome components in the early-diverging protist Giardia lamblia. This organism is particularly interesting because it possesses a very unusual splicing system, contains relatively few introns, and appears to be undergoing intron loss as it reduces its genome size and further adapts to its parasitic lifestyle. We will also characterize gene expression pathways and cellular components used for ncRNA synthesis in these protists, and exploit their evolutionary positions to derive insights about ncRNA and spliceosome evolution in eukaryotes.