Abstract
Microsatellite expansions cause more than 40 neurological disorders, including Huntington's disease, myotonic dystrophy, and C9ORF72 amyotrophic lateral sclerosis/frontotemporal dementia (ALS/FTD). These repeat expansion mutations can produce repeat-associated non-ATG (RAN) proteins in all three reading frames, which accumulate in disease-relevant tissues. There has been considerable interest in RAN protein products and their downstream consequences, particularly for the dipeptide proteins found in C9ORF72 ALS/FTD. Understanding how RAN translation occurs, what cellular factors contribute to RAN protein accumulation, and how these proteins contribute to disease should lead to a better understanding of the basic mechanisms of gene expression and human disease.
Keywords:
C9ORF72 ALS/FTD; Huntington's disease; RAN translation; amyotrophic lateral sclerosis (ALS) (Lou Gehrig disease); mouse models; myotonic dystrophy; nucleocytoplasmic transport; spinocerebellar ataxia; translation; translation initiation; trinucleotide repeat disease.
© 2018 Cleary et al.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Amyotrophic Lateral Sclerosis / genetics
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C9orf72 Protein
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DNA Repeat Expansion*
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Dipeptides
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Frontotemporal Dementia / genetics
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Gene Expression
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Huntington Disease / genetics
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Microsatellite Repeats*
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Mutation
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Myotonic Dystrophy / genetics
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Nervous System Diseases* / genetics
Substances
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C9orf72 Protein
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C9orf72 protein, human
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Dipeptides
Supplementary concepts
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Frontotemporal Dementia With Motor Neuron Disease