Imed Gallouzi

Academic title(s): 

Professor, Associate Chair (Education), Department of Biochemistry

Imed Gallouzi
Contact Information
Address: 

McIntyre Medical Sciences Building
3655 promenade Sir-William-Osler
Office: Room 915B; Lab: Room 915
Montreal, Quebec H3G 1Y6

Email address: 
imed.gallouzi [at] mcgill.ca
Phone: 
Office: 514-398-4537
Lab: 514-398-4989
Department: 
Biochemistry
Goodman Cancer Institute
Area(s): 
Cancer
Cell and Molecular Biology
Degree(s): 

1998 - PhD, Graduate School of Biology and Health, Montpellier, France

Current research: 

mRNA metabolism during the cell cycle; cell differentiation

Our general research area is mRNA metabolism during the cell cycle and cell differentiation. We use the tools of molecular and cell biology to study problems in this field. The long-term research goals focus on understanding the cellular mechanisms involved in the regulation of mRNA half-lives and how they affect cell growth and differentiation.

mRNA stability influences gene expression in virtually all organisms, from bacteria to mammals. In mammalian cells, the abundance of a particular mRNA can fluctuate dramatically due to a change in mRNA half-life, without any change in transcription. The processes that regulate mRNA half-lives can thus affect how a cell grows, differentiates and responds to its environment.

Understanding these processes requires a combination of different approaches; molecular biology and biochemistry techniques will help to understand the molecular mechanisms by which mRNA stability and degradation are regulated during cell division and differentiation and the cell biological technology will help to establish the connection between them. Towards these goals, we are using and developing in vitro, in vivo and ex-vivo methods to facilitate the identification and the characterization of factors involved in the stabilization as well as in the degradation of mRNAs in mammalian cells.

Although these two phenomena are well-studied separately, very little is known about how they are integrated inside the cell. We do not know the factors that bridge and thus allow cross talk between the two processes. Since many cancer cells exhibit changes in mRNA half-lives, a precise balance between the two processes is needed to preserve cell integrity. Therefore, it is important to define the link between mRNA stabilization and degradation, and to establish how both are regulated inside the cell. Making this connection will help to clarify how and why many cancers start and will provide new targets for future therapy.

 

Selected publications: 
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