Details

Autor(en) / Beteiligte

• Rodriguez, Caitlin M
• Wright, Shannon E
• Kearse, Michael G
• Haenfler, Jill M
• Flores, Brittany N
• Liu, Yu
• Ifrim, Marius F
• Glineburg, Mary R
• Krans, Amy
• Jafar-Nejad, Paymaan
• Sutton, Michael A
• Bassell, Gary J
• Parent, Jack M
• Rigo, Frank
• Barmada, Sami J
• Todd, Peter K

Titel

A native function for RAN translation and CGG repeats in regulating fragile X protein synthesis

Ist Teil von

• Nature neuroscience, 2020-03, Vol.23 (3), p.386-397

Ort / Verlag

United States

Erscheinungsjahr

2020

Quelle

MEDLINE

Beschreibungen/Notizen

• Repeat-associated non-AUG-initiated translation of expanded CGG repeats (CGG RAN) from the FMR1 5'-leader produces toxic proteins that contribute to neurodegeneration in fragile X-associated tremor/ataxia syndrome. Here we describe how unexpanded CGG repeats and their translation play conserved roles in regulating fragile X protein (FMRP) synthesis. In neurons, CGG RAN acts as an inhibitory upstream open reading frame to suppress basal FMRP production. Activation of mGluR5 receptors enhances FMRP synthesis. This enhancement requires both the CGG repeat and CGG RAN initiation sites. Using non-cleaving antisense oligonucleotides (ASOs), we selectively blocked CGG RAN. This ASO blockade enhanced endogenous FMRP expression in human neurons. In human and rodent neurons, CGG RAN-blocking ASOs suppressed repeat toxicity and prolonged survival. These findings delineate a native function for CGG repeats and RAN translation in regulating basal and activity-dependent FMRP synthesis, and they demonstrate the therapeutic potential of modulating CGG RAN translation in fragile X-associated disorders.