Mailing address: University of Waterloo: Biology 1 – 377B, 200 University Ave. W. Waterloo, Ontario, Canada, N2L 3G1
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Phone: 519.573.3349
Office: Biology 1, room 377B, University of Waterloo
CANCELLED
Presented by:
Joseph Bondy-Denomy, PhD
Assistant Professor
University of California, San Francisco
Dept. of Microbiology & Immunology
Membrane bound organelles are a central tenant of eukaryotic cell biology, and largely absent from prokaryotes. However, protein-encased structures have been identified in bacteria, for example encapsulins and carboxysomes that localize enzymes, but none that compartmentalize nucleic acid. However, recent work has described the discovery of a prokaryotic proteinaceous compartment that mirrors a nucleus, localizing DNA replication and transcription into a centrally located, segregated structure, while translation happens in the cytoplasm. Intriguingly, this structure is made inside a bacterium, but not by the bacterium. This process is entirely directed by a bacterial virus, or bacteriophage. I will discuss this remarkable structure and our recent findings that this proteinaceous nucleus-like compartment segregates phage DNA from restriction and CRISPR-Cas nucleases, providing the most broad spectrum resistance to bacterial immune pathways described to date. This will be contrasted with specific inhibitors of CRISPR-Cas function, or “anti-CRISPR” proteins, also encoded by phage that our group has identified.
The University of Waterloo acknowledges that much of our work takes place on the traditional territory of the Neutral, Anishinaabeg and Haudenosaunee peoples. Our main campus is situated on the Haldimand Tract, the land granted to the Six Nations that includes six miles on each side of the Grand River. Our active work toward reconciliation takes place across our campuses through research, learning, teaching, and community building, and is centralized within our Office of Indigenous Relations.