Grant: Discovery Grants Program - Individual
University of Alberta
$138,000.00
Exploring the evolution of the Contractile Vacuole.
FY 2023-24
Summary
Movement of material within the cell, as well as import, export, and cell surface presentation is mediated by the membrane trafficking system (MTS). Its appropriate and successful operation underpins effective cellular function, whether in plants of agricultural importance, parasites of economic impact or algae and protists key to ecosystem balance. Evolving an MTS was key to establishing the eukaryotic cellular configuration and giving rise to nearly all of the biological diversity that we see today. My research program examines the patterns and processes driving the evolution of the MTS. This work provides insights into the fundamental forces that shaped our cellular history and yields important information about modern cell biology. Intriguingly, we have uncovered protein machinery widely present outside of animals and fungi: the cell biology of membrane-trafficking in diverse eukaryotes may differ from well-characterized model systems in ways that are only beginning to be understood. Similarly, while some membrane-trafficking organelles are conserved across eukaryotes, poorly understood organelles are present outside the well-known model systems that are ripe for exploration. The Contractile Vacuole (CV) is an osmoregulatory organelle found in ecologically important freshwater and soil-dwelling organisms. However, it is often not reported as present in parasites or marine organisms, raising questions of whether organelles identified as contractile vacuoles are truly orthologous between diverse eukaryotes. We will use molecular evolutionary and transcriptomic analysis to examine the evolution and function of the CV by two short-term goals, each with sub-projects defined within them. 1: In order to test the simplest null hypothesis that the CV derived from a single homologous ancestor, a sampling of eukaryotes with CVs from across the eukaryotic tree will be investigated. Transcriptomics will be used to determine genes that are differentially expressed upon induction of CV function by osmotic stress. The identity and evolution of these genes will be assessed with the explicit prediction that a common core gene set associated with CV function would imply homology. 2: To complement this taxonomically broad approach, analysis will be focused on a single lineage possessing well-characterized CVs, the ciliates. Molecular evolutionary and transcriptomics across the full taxonomic range of ciliates will assess the machinery that is conserved in CV function, again predicting the presence of a conserved core set. By identifying the genes of importance in CV function and their distribution in eukaryotes, we gain information about the workings of an organelle present in ecologically crucial lineages of eukaryotes. By understanding the evolution of the CV, we will be able to integrate an important organelle into the larger framework of membrane-trafficking evolution and gain a better understanding into the rise of eukaryotic life on Earth.
Program
Discovery Grants Program - Individual
Recipient
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
RGPIN-2019-06109
Name nom
Dacks, Joel
Department département
Cell Biology - Cell Biology
Organization id
9
Institution établissement
University of Alberta
Province en
Alberta
Province fr
Alberta
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2023
Competition year année de concours
2019
Award amount
138000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR 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
4709
Research subject group en
Evolution and ecology
Research subject group fr
Taxonomy, systematics and phylogenetics
Research subject en
Évolution et écologie
Research subject fr
Taxonomie, systématique et phylogénétique
Application title
Exploring the evolution of the Contractile Vacuole.
Keyword
Endolysosomal organelle; Evolutionary Cell Biology; Freshwater organism; Genomics; Membrane-trafficking system; Osmoregulation; Protistology; RNASeq
Application summary
Movement of material within the cell, as well as import, export, and cell surface presentation is mediated by the membrane trafficking system (MTS). Its appropriate and successful operation underpins effective cellular function, whether in plants of agricultural importance, parasites of economic impact or algae and protists key to ecosystem balance. Evolving an MTS was key to establishing the eukaryotic cellular configuration and giving rise to nearly all of the biological diversity that we see today. My research program examines the patterns and processes driving the evolution of the MTS. This work provides insights into the fundamental forces that shaped our cellular history and yields important information about modern cell biology. Intriguingly, we have uncovered protein machinery widely present outside of animals and fungi: the cell biology of membrane-trafficking in diverse eukaryotes may differ from well-characterized model systems in ways that are only beginning to be understood. Similarly, while some membrane-trafficking organelles are conserved across eukaryotes, poorly understood organelles are present outside the well-known model systems that are ripe for exploration. The Contractile Vacuole (CV) is an osmoregulatory organelle found in ecologically important freshwater and soil-dwelling organisms. However, it is often not reported as present in parasites or marine organisms, raising questions of whether organelles identified as contractile vacuoles are truly orthologous between diverse eukaryotes. We will use molecular evolutionary and transcriptomic analysis to examine the evolution and function of the CV by two short-term goals, each with sub-projects defined within them. 1: In order to test the simplest null hypothesis that the CV derived from a single homologous ancestor, a sampling of eukaryotes with CVs from across the eukaryotic tree will be investigated. Transcriptomics will be used to determine genes that are differentially expressed upon induction of CV function by osmotic stress. The identity and evolution of these genes will be assessed with the explicit prediction that a common core gene set associated with CV function would imply homology. 2: To complement this taxonomically broad approach, analysis will be focused on a single lineage possessing well-characterized CVs, the ciliates. Molecular evolutionary and transcriptomics across the full taxonomic range of ciliates will assess the machinery that is conserved in CV function, again predicting the presence of a conserved core set. By identifying the genes of importance in CV function and their distribution in eukaryotes, we gain information about the workings of an organelle present in ecologically crucial lineages of eukaryotes. By understanding the evolution of the CV, we will be able to integrate an important organelle into the larger framework of membrane-trafficking evolution and gain a better understanding into the rise of eukaryotic life on Earth.