101. Toxic expanded GGGGCC repeat transcription is mediated by the PAF1 complex in C9orf72-associated FTD
- Author
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Casey Cook, Michael Parisi, Luis F. Martinez-Ramirez, Ananth R. Srinivasan, Nicholas J. Kramer, Nancy M. Bonini, Jeannie Chew, Amit Berson, Aaron D. Gitler, Yongqing Zhu, Matthews Lan, Mercedes Prudencio, Lindsey D. Goodman, and Leonard Petrucelli
- Subjects
0301 basic medicine ,RNA polymerase II ,Article ,03 medical and health sciences ,Mice ,0302 clinical medicine ,Transcription (biology) ,C9orf72 ,Transcriptional regulation ,Animals ,Humans ,Gene ,DNA Repeat Expansion ,biology ,C9orf72 Protein ,General Neuroscience ,RNA ,Nuclear Proteins ,Molecular biology ,Chromatin ,030104 developmental biology ,Drosophila melanogaster ,Gene Expression Regulation ,Frontotemporal Dementia ,biology.protein ,Trinucleotide repeat expansion ,Neuroscience ,030217 neurology & neurosurgery ,Transcription Factors - Abstract
An expanded GGGGCC hexanucleotide of more than 30 repeats (termed (G4C2)30+) within C9orf72 is the most prominent mutation in familial frontotemporal degeneration (FTD) and amyotrophic lateral sclerosis (ALS) (termed C9+). Through an unbiased large-scale screen of (G4C2)49-expressing Drosophila we identify the CDC73/PAF1 complex (PAF1C), a transcriptional regulator of RNA polymerase II, as a suppressor of G4C2-associated toxicity when knocked-down. Depletion of PAF1C reduces RNA and GR dipeptide production from (G4C2)30+ transgenes. Notably, in Drosophila, the PAF1C components Paf1 and Leo1 appear to be selective for the transcription of long, toxic repeat expansions, but not shorter, nontoxic expansions. In yeast, PAF1C components regulate the expression of both sense and antisense repeats. PAF1C is upregulated following (G4C2)30+ expression in flies and mice. In humans, PAF1 is also upregulated in C9+-derived cells, and its heterodimer partner, LEO1, binds C9+ repeat chromatin. In C9+ FTD, PAF1 and LEO1 are upregulated and their expression positively correlates with the expression of repeat-containing C9orf72 transcripts. These data indicate that PAF1C activity is an important factor for transcription of the long, toxic repeat in C9+ FTD. The (G4C2)30+ repeat expansion is the most prominent mutation in familial FTD and ALS. Here the PAF1 complex is identified as a transcriptional regulator of this unique mutation. Data from FTD tissue positive for the C9orf72 mutation support the relevance of this complex in disease.
- Published
- 2019