Robert Sladek, MD
Assistant Professor of Medicine
Biographical Sketch
Rob Sladek is an Assistant Professor at the McGill University and
Genome Quebec Innovation Centre. He completed undergraduate studies in Engineering
Science and Medicine as well as a clinical fellowship in Endocrinology and
Metabolism, all at the University of Toronto. His postdoctoral training explored
the role of the Estrogen-related receptors in the regulation of fat metabolism and
reproduction (with Dr Vincent Gigu�re) and the application of high-throughput
genomics technologies to study complex traits (with Dr Tom Hudson). His current
research centers on the development of new technologies for studying the dynamics
of gene transcription networks in living cells (the Living Microarray Project) and
risk factors for type 2 diabetes (the Diabetes Gene Discovery Group).
Selected Scientific Contributions
Dr Sladek's scientific contributions centre on establishing the
role of gene transcription networks in complex traits. He identified key physiological
roles for the orphan nuclear receptor ERRalpha in regulating the balance between
lipolysis and lipogenesis and ERRbeta in regulating development of the chorion and
trophoblast. He has developed methods to identify transcriptional networks de novo
in panels of recombinant congenic mouse strains and to characterize transcriptional
effects of cis-regulatory genetic variants that underlie complex genetic traits. Most
recently, he collaborated with Drs Froguel, Polychronakos, Posner and Prentki to
complete the first genome-wide association study (GWAS) to identify risk loci for
type 2 diabetes.
Click here for PubMed listing
Research Interests
Current projects in the laboratory include:
The Living Microarray Project. In collaboration
with Hans De Sterck (Waterloo), Justin Wan (Waterloo), Tom Hudson (Toronto), Bernhard
Bodmann (Houston), Haig Djambazian and Sarav Sundararajan (McGill), I am developing
a high-throughput imaging platform to identify and characterize gene transcription
networks in living cells. The platform is able simultaneously image hundreds of
fluorescent reporter constructs during cell division and differentiation (including
myogenesis).
Functional characterization of risk loci for type 2
diabetes. In collaboration with Mike Wheeler (Toronto), Jarred Chicoine
and Albena Pramatarova (McGill), I am involved in characterizing the effects of
diabetes risk loci on beta-cell physiology and particularly the effects of SLC30A8
coding variants on zinc transport, beta-cell viability and insulin secretion.
The Gene Regulation in Disease (GRiD) project.
In collaboration with Tomi Pastinen, Jacek Majewski and Huan Chu Pham Dang (McGill),
I am involved in developing strategies to identify causative genetic polymorphisms
that underlie disease risk loci and determine their effects on cell physiology and
gene regulation.
Nanomedicine Sensors project. This collaboration,
with Peter Grutter, Bruce Lennox and John White seeks to develop novel sensors to
measure nucleic acid levels in vivo. These technologies, based on atomic force
microscopy and gold nanoparticles will be used to provide rapid and sensitive assays
to detect single nucleotide polymorphisms and to measure gene transcription from
endogenous loci in real time.
Diabetes Gene Discovery Group. This multicentre
collaboration, with Philippe Froguel, Ghislain Rocheleau, David Serre, Marcin Swiatek,
Christian Dina, Nabila Bouatia-Naji, David Meyre, Stephane Cauchy, Martine Vaxillaire,
Johan Rung, Lishaung Shen, Alexander Mazur and Constantin Polychronakos seeks to
identify genetic variants that predispose to type 2 diabetes.
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