Daniela C. Zarnescu
Postdoctoral Research Fellow
(404) 727-4815 - phone
(404) 727-4717 - fax
zarnescu@cellbio.emory.edu

 

Research Interests
I am interested in Fragile-X syndrome, which includes mental and physical defects and is the most common form of inherited mental retardation. I recently conducted a genetic screen for dominant modifiers of the Drosophila Fmr1 misexpression phenotype in the compound eye. In screening 51, 000 mutant individuals I discovered 5 complementation groups consisting of at least 2 alleles each. The screen unraveled a major complementation group, which consists of 19 alleles and maps to the previously known lethal (2) giant larvae locus. Fmr1 protein and Lgl associate in vivo in flies and mice. In addition to the genetic interaction in the retina, Drosophila l(2)gl enhances the loss of function phenotype of dfmr1 mutants at the neuromuscular junction. Taken together, our data suggests that Lgl acts upstream of Fmr1, perhaps aiding in transport of mRNAs associated with Fmr1, or in anchoring the latter to specific membrane domains.

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