Biology Seminar Series

Biology Seminar Series

Categories: Lectures and Seminars | Intended for

Friday, March 14, 2014

3:30 PM - 4:30 PM | Add to calendar

4440q Carleton Technology and Training Centre

1125 Colonel By Dr, Ottawa, ON

Contact Information

Dr. Bruce McKay, 613-520-2478,


No registration required.



About this Event

Host Organization: Biology Department

The role of protein arginine methyltransferases in cancer

Dr. Mitch Baldwin, Cellular and Molecular Medicine, University of Ottawa

Friday, March 14th – 3:30PM – CTTC 4440Q

Faculty Host: Bruce McKay

Cancer • Post-Translational Modification • Alternative Splicing


Abstract from recent paper: Protein arginine methylation is catalyzed by protein arginine methyltransferases (PRMTs) and plays an important role in many cellular processes. Aberrant PRMT expression has been observed in several common cancer types; however, their precise contribution to the cell transformation process is not well understood. We previously reported that the PRMT1 gene generates several alternatively spliced isoforms, and our initial biochemical characterization of these isoforms revealed that they exhibit distinct substrate specificity and subcellular localization. We focus here on the PRMT1v2 isoform, which is the only predominantly cytoplasmic isoform, and we have found that its relative expression is increased in breast cancer cell lines and tumors. Specific depletion of PRMT1v2 using RNA interference caused a significant decrease in cancer cell survival due to an induction of apoptosis. Furthermore, depletion of PRMT1v2 in an aggressive cancer cell line significantly decreased cell invasion. We also demonstrate that PRMT1v2 overexpression in a non-aggressive cancer cell line was sufficient to render them more invasive. Importantly, this novel activity is specific to PRMT1v2, as overexpression of other isoforms did not enhance invasion. Moreover, this activity requires both proper subcellular localization and methylase activity. Lastly, PRMT1v2 overexpression altered cell morphology and reduced cell-cell adhesion, a phenomenon that we convincingly linked with reduced β-catenin protein expression. Overall, we demonstrate a specific role for PRMT1v2 in breast cancer cell survival and invasion, underscoring the importance of identifying and characterizing the distinct functional differences between PRMT1 isoforms.