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Altered translational repression of an RNA‐binding protein, Elav by AOA2‐causative Senataxin mutation
Author(s) -
Choudhury Saumitra Dey,
VS Ancy,
Mushtaq Zeeshan,
Kumar Vimlesh
Publication year - 2017
Publication title -
synapse
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.809
H-Index - 106
eISSN - 1098-2396
pISSN - 0887-4476
DOI - 10.1002/syn.21969
Subject(s) - biology , rna , amyotrophic lateral sclerosis , genetics , ataxia , transcription (linguistics) , gene , microbiology and biotechnology , psychological repression , mutation , mutant , tardbp , rna binding protein , gene expression , neuroscience , sod1 , medicine , linguistics , philosophy , disease , pathology
Abstract Mutations in Senataxin (SETX) gene causes two types of neurological disorders, Amyotrophic Lateral Sclerosis (ALS4) and Ataxia with Oculomotor Apraxia type 2 (AOA2). Recent studies in cultured cells suggest that SETX plays a crucial role at the interface of transcription and the DNA damage response. Whether SETX can alter translational of specific RNA is not known. In this study, we report that expressing AOA2‐causative truncated form of human SETX in Drosophila neurons alters the development of neuromuscular junction (NMJ) synapses. Interestingly, we found that expressing this truncated form of SETX in Drosophila muscles resulted in an alteration of translational repression of an RNA‐binding protein, Embryonic Lethal Abnormal Vision (Elav). Elav is transcribed in all tissues but remains translationally repressed except in neurons. Thus, our data suggest that an altered repression profile of RNA by SETX mutants could be one of the mechanisms underlying ALS4 or AOA2 pathogenesis.