Trinucleotide repeat instability underlies >20 human hereditary disorders. These diseases include many neurological and neurodegenerative situations, such as those caused by pathogenic polyglutamine (polyQ) domains encoded by expanded CAG repeats. Although mechanisms of instability have been intensely studied, our knowledge remains limited in part due to the lack of unbiased genome-wide screens in multicellular eukaryotes. Drosophila melanogaster displays triplet repeat instability with features that recapitulate repeat instability seen in patients with disease. Here we report an enhanced fly model with substantial instability based on a noncoding 270 CAG (UAS - CAG 270) repeat construct under control of a germline-specific promoter. We find that expression of pathogenic polyQ protein modulates repeat instability of CAG 270 in trans, indicating that pathogenic-length polyQ proteins may globally modulate repeat instability in the genome in vivo. We further performed an unbiased genetic screen for novel modifiers of instability. These studies indicate that different aspects of repeat instability are under independent genetic control, and identify CG15262, a protein with a NOT2/3/5 conserved domain, as a modifier of CAG repeat instability in vivo. Copyright,
Genetics (Print): a periodical record of investigations bearing on heredity and variation
Department of Medical Oncology

Jung, J., van Jaarsveld, M., Shieh, S.-Y., Xu, K., & Bonini, N. M. (2011). Defining genetic factors that modulate intergenerational CAG repeat instability in Drosophila melanogaster. Genetics (Print): a periodical record of investigations bearing on heredity and variation, 187(1), 61–71. doi:10.1534/genetics.110.121418