Sylvie Doublié, Ph.D.

Rubriques

Sylvie Doublié, Ph.D.
Title
Professor
Department
Department of Microbiology and Molecular Genetics
Institution
University of Vermont
Address
E314A Given Building
89 Beaumont Avenue
City, State, ZIP
Burlington, VT 5405
Phone
(802) 656-9531
Email
[email protected]
Website
http://www.uvm.edu/microbiology/directory/mmg-faculty-directory/faculty-details/?people_id=89
Research field
Structural Biology
Award year
2000

Research

The major thrust of my research program is to study modifications in DNA or RNA in the context of the enzymes and proteins that generate and recognize them. Researchers in my lab are pursuing three general areas of investigation. 1) DNA polymerases, which otherwise faithfully replicate DNA, stumble when they encounter oxidative DNA lesions. Polymerases either will be blocked at the site of lesion, or bypass it. The latter case, referred to as translesion synthesis, may initiate an oncogenic process if the wrong base is inserted opposite the lesion. One aim is focused on uncovering the fundamental mechanisms underpinning translesion synthesis, which is paramount to understanding the initial events of mutagenesis. A second aim of the lab is studying Base Excision Repair (BER). Several DNA repair mechanisms are in place to minimize damage in DNA before DNA polymerases replicate the genome. One of these processes is called Base Excision Repair (BER). The goal of this project is to delineate the structural features of the DNA glycosylases that are involved in recognition of DNA base damage produced by ionizing radiation. Lastly, we are investigating Messenger RNA (mRNA) modifications. During processing of the 3’-end of mRNA, an endonucleolytic cleavage event precedes the addition of a poly(A) tail. Such maturation of 3’-ends is a key regulatory step in the expression of many genes. The cleavage and polyadenylation reactions are carried out by a multicomponent machinery of remarkable complexity. Our goal is to understand how the different components of the machinery interact to cleave then polyadenylate messenger RNAs.

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