Repeat-associated non-AUG translation in neuromuscular diseases: mechanisms and therapeutic insights

Author:

Fujino Yuzo12,Mori Kohji3,Nagai Yoshitaka14

Affiliation:

1. Faculty of Medicine, Kindai University Department of Neurology, 377-2 Ohnohigashi, Osaka-sayama, Osaka 589-8511, Japan

2. Kyoto Prefectural University of Medicine Department of Neurology, , 465 Kajii-cho, Kamigyo-ku, Kyoto, Kyoto 602-8566, Japan

3. Osaka University Graduate School of Medicine Department of Psychiatry, , D3, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan

4. Life Science Research Institute, Kindai University 377-2 Ohnohigashi , Osaka-Sayama, Osaka 589-8511, Japan

Abstract

Summary Expanded short tandem repeats cause more than 50 monogenic diseases, which are mostly neuromuscular diseases. In the non-coding repeat expansion diseases, in which the expanded repeat sequence is located outside of the coding region, the toxicity of the transcribed repeat-containing RNAs had been the focus of research. However, recent studies have revealed that repeat RNAs can be translated into repeat polypeptides, despite the lack of an AUG initiation codon, by non-canonical repeat-associated non-AUG translation (RAN translation). RAN translated repeat polypeptides have actually been confirmed in patients’ tissues. Moreover, various cellular and animal disease models have demonstrated the toxicity of these peptides, suggesting the pathogenic roles of RAN translation in the repeat expansion diseases. In this review, we will outline RAN translation, from the viewpoint of its molecular mechanisms to its potential as a therapeutic target for the repeat expansion diseases.

Funder

Japan Society for the Promotion of Science

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Biochemistry,General Medicine

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