Dr. Steve Bilodeau is an associate professor at Laval University (Department of Molecular Biology, Medical Biochemistry and Pathology, School of Medicine) and has been a principal investigator for the oncology axis of the Centre de recherche du CHU de Québec-Laval University, since 2012. In addition to being finalist for the Maud-Menten New Principal Investigator prize, Dr. Bilodeau holds the Canada Research Chair in transcriptional genomics.
Since his training at the prestigious Massachusetts Institute of Technology (MIT, 2007-2012), Dr. Bilodeau has studied the molecular mechanisms controlling gene expression during normal and disease development. Indeed, despite common genetic material, each cell has a unique gene expression program that is specific to its function. An imbalance in this program changes the daily operations of the cell; instructing a new role in the process. Therapeutic approaches currently focus on the destruction of defective cells or on treating symptoms associated with the disease. The premise of Dr. Bilodeau’s lab is that, if the gene expression program can be controlled, all cells, healthy or diseased, can be controlled as well.
Dr. Bilodeau’s research is funded by the Canadian Institutes of Health Research (CIHR) and the Natural Sciences and Engineering Research Council of Canada (NSERC). His work aims to integrate the multiple layers of information from the nuclear environment (chromosome structure, chromatin, regulators, etc.) in order to determine which genes are prioritized by a given cell during a transcriptional response triggered by an environmental change. More specifically, Dr. Bilodeau’s team seeks to understand the biological role of the three-dimensional organization of the genome in the communication between genes. The findings of Dr. Bilodeau’s team provide the basic information needed to understand the role of noncoding regulatory regions, which frequently harbor genetic events associated with multiple diseases, in maintaining the transcriptional program. This problem affects both developmental syndromes and cancers.
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ZNF768 links oncogenic RAS to cellular senescence.Journal Article
Nat Commun, 12 (1), 2021.
Modulating HSF1 levels impacts expression of the estrogen receptor α and antiestrogen response.Journal Article
Life Sci Alliance, 4 (5), 2021.
Proximity-dependent Mapping of the Androgen Receptor Identifies Kruppel-like Factor 4 as a Functional Partner.Journal Article
Mol Cell Proteomics, 20 , 2021.
Control of adipogenic commitment by a STAT3-VSTM2A axis.Journal Article
Am J Physiol Endocrinol Metab, 320 (2), 2021.
Defining the Transcriptional Ecosystem.Journal Article
Mol Cell, 72 (6), 2018.
Author Correction: Enhancer decommissioning by LSD1 during embryonic stem cell differentiation.Journal Article
Nature, 562 (7728), 2018.
Connected Gene Communities Underlie Transcriptional Changes in Cornelia de Lange Syndrome.Journal Article
Genetics, 207 (1), 2017.
FOXA and master transcription factors recruit Mediator and Cohesin to the core transcriptional regulatory circuitry of cancer cells.Journal Article
Sci Rep, 6 , 2016.
metagene Profiles Analyses Reveal Regulatory Element's Factor-Specific Recruitment Patterns.Journal Article
PLoS Comput Biol, 12 (8), 2016.
Mutant cohesin affects RNA polymerase II regulation in Cornelia de Lange syndrome.Journal Article
Sci Rep, 5 , 2015.
- Chaire de recherche du Canada en génomique transcriptionnelle, from 2017-09-01 to 2022-08-31
- Defining the global transcriptional response to perturbations, from 2021-04-01 to 2026-03-31
- Elucidation of bromodomain functions within SWI/SNF complexes, from 2020-04-01 to 2025-03-31
- Toward defining the transcriptional ecosystem, from 2019-04-01 to 2024-03-31
- Using BET bromodomain inhibitors to create phenotypic lethality in melanoma, from 2020-09-01 to 2022-08-31
Recently finished projects
- Efficient and reliable shearing of chromatin for highthroughput analysis, from 2019-03-28 to 2020-03-31
- Elucidation of bromodomain functions within SWI/SNF complexes (Prix), from 2020-03-01 to 2021-02-28
- Toward nutritional and epigenomic interventions in prostate cancer prevention and management, from 2017-10-01 to 2020-09-30