We found a match
Your institution may have rights to this item. Sign in to continue.
- Title
Transcriptional dysregulation by a nucleus-localized aminoacyl-tRNA synthetase associated with Charcot-Marie-Tooth neuropathy.
- Authors
Bervoets, Sven; Wei, Na; Erfurth, Maria-Luise; Yusein-Myashkova, Shazie; Ermanoska, Biljana; Mateiu, Ligia; Asselbergh, Bob; Blocquel, David; Kakad, Priyanka; Penserga, Tyrone; Thomas, Florian P; Guergueltcheva, Velina; Tournev, Ivailo; Godenschwege, Tanja; Jordanova, Albena; Yang, Xiang-Lei
- Abstract
Charcot-Marie-Tooth disease (CMT) is a length-dependent peripheral neuropathy. The aminoacyl-tRNA synthetases constitute the largest protein family implicated in CMT. Aminoacyl-tRNA synthetases are predominantly cytoplasmic, but are also present in the nucleus. Here we show that a nuclear function of tyrosyl-tRNA synthetase (TyrRS) is implicated in a Drosophila model of CMT. CMT-causing mutations in TyrRS induce unique conformational changes, which confer capacity for aberrant interactions with transcriptional regulators in the nucleus, leading to transcription factor E2F1 hyperactivation. Using neuronal tissues, we reveal a broad transcriptional regulation network associated with wild-type TyrRS expression, which is disturbed when a CMT-mutant is expressed. Pharmacological inhibition of TyrRS nuclear entry with embelin reduces, whereas genetic nuclear exclusion of mutant TyrRS prevents hallmark phenotypes of CMT in the Drosophila model. These data highlight that this translation factor may contribute to transcriptional regulation in neurons, and suggest a therapeutic strategy for CMT. Tyrosyl-tRNA synthetase (TyrRS) is a translation factor and predominantly cytoplasmic, but can also be found in the nucleus. Here authors show using a fly model of Charcot-Marie-Tooth (CMT) disease that nuclear localization of mutant TyrRS contributes to the CMT-like phenotype.
- Subjects
GENE regulatory networks; CELL nuclei; AMINOACYL-tRNA synthetases; CHARCOT-Marie-Tooth disease; NEUROPATHY
- Publication
Nature Communications, 2019, Vol 10, Issue 1, pN.PAG
- ISSN
2041-1723
- Publication type
Article
- DOI
10.1038/s41467-019-12909-9