Keyword: Cell biology and genetics

Shaun Sanders

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The Sanders lab is interested in how neurons use the protein-lipid modification palmitoylation to target proteins to subcellular locations and to define how palmitoylation-dependent targeting contributes to physiological neuronal function and neuropathological conditions. Current projects include characterizing how palmitoylation of vesicular transport machinery regulates fast axonal transport and how palmitoylation of ion channels and their scaffold proteins regulates clustering at the axon initial segment, a critical site of neuronal excitability where action potentials are generated.

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Paul Hebert

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Morphological studies have provided an outline of biodiversity, but are incapable of surveying, managing and protecting it on a planetary scale. By exploiting two technologies that are gaining power exponentially – DNA sequencing and computational capacity – my research promises an ever-accelerating capacity to monitor and know life. In particular, I aim to automate species identification and discovery, and to employ this capacity to answer longstanding scientific questions. Automation is possible because sequence diversity in short, standardized gene regions (DNA barcodes) enables fast, cheap, and accurate species discrimination. New instruments can inexpensively gather millions of DNA sequences, enabling surveys of organismal diversity at speeds and scales that have been impossible.

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Ian Tetlow

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My lab examines the control mechanisms underpinning starch biosynthesis in leaf chloroplasts (which make starch during the daytime, and degrade it at night) of the model plant Arabidopsis thaliana, and non-photosynthetic amyloplasts of cereal endosperms such as maize, wheat, barley and rice which make storage starches. More specifically, we are interested in the biochemical control mechanisms governing the many enzymes and enzyme classes which make up the core pathway of starch biosynthesis. This involves investigating the role of protein-protein interactions and protein phosphorylation in coordinating the proteins involved in starch synthesis and degradation within the plastid to produce the highly ordered and complex structure of the starch granule.

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Scott Ryan

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While animal models have lead to huge advancements in our understanding of neurobiology, there is controversy over whether overexpression/silencing of gene expression is representative of diverse disease states. Indeed, the lack of availability of primary human neurons has made evaluating the pathological consequences of genomic mutations arduous. The use of human induced pluripotent stem cell (hiPSC) technology overcomes these limitations by providing a source of human neurons from both normal and disease genetic backgrounds. We currently focus on stem cell based models of Parkinson's Disease (PD) to study how mitochondrial stress mechanisms impact on neuronal function in human disease.

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Teresa Crease

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Research in the Crease lab uses freshwater crustaceans in the genus Daphnia as a model organism to study evolution of the ribosomal (r)DNA multigene family, and of the DNA transposon, Pokey, which inserts in a specific region of the Daphnia rDNA repeat as well as other genomic locations. Current projects involve comparing rates of evolution in ribosomal proteins that bind to conserved and variable regions of rRNA genes, determining the impact of breeding system (cyclic or obligate parthenogenesis) on the evolution of rDNA and Pokey transposons, determining the relationship between rDNA copy number and Pokey distribution, and measuring rates of Pokey transposition inside and outside of rDNA.

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Todd Gillis

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Ongoing projects include:
1) Examining cardiac remodeling in zebrafish and trout in response to thermal acclimation.
2) Characterizing the role of the troponin complex in regulating the function of striated muscle.
3) Examining the function of the hagfish heart during prolonged anoxia exposure.
4) Examining the change in diaphragm function during the onset of heart failure.
5) Characterizing how bitumen exposure of sockeye salmon early life stages influences cardiac development and aerobic fitness.

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Jennifer Geddes-McAlister

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We are interested in characterizing the mechanisms of pathogenesis, adaptation, and survival in fungal and bacterial microbes from a systems biology perspective through mass spectrometry-based quantitative proteomics. Specifically, research in the lab centres around the following areas:
1) Systems biology to elucidate microbial proteome dynamics and interactions;
2) Mechanistic characterization of pathogenic proteins; and
3) Mass spectrometry-based proteomics for drug discovery and repurposing.

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