hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations.
Acta Neuropathol
; 125(3): 413-23, 2013 Mar.
Article
en En
| MEDLINE
| ID: mdl-23381195
ABSTRACT
Genetic analysis revealed the hexanucleotide repeat expansion GGGGCC within the regulatory region of the gene C9orf72 as the most common cause of familial amyotrophic lateral sclerosis and the second most common cause of frontotemporal lobar degeneration. Since repeat expansions might cause RNA toxicity via sequestration of RNA-binding proteins, we searched for proteins capable of binding to GGGGCC repeats. In vitro-transcribed biotinylated RNA containing hexanucleotide GGGGCC or, as control, AAAACC repeats were incubated with nuclear protein extracts. Using stringent filtering protocols 20 RNA-binding proteins with a variety of different functions in RNA metabolism, translation and transport were identified. A subset of these proteins was further investigated by immunohistochemistry in human autopsy brains. This revealed that hnRNP A3 formed neuronal cytoplasmic and intranuclear inclusions in the hippocampus of patients with C9orf72 repeat extensions. Confocal microcopy showed that these inclusions belong to the group of the so far enigmatic p62-positive/TDP-43 negative inclusions characteristically seen in autopsy cases of diseased C9orf72 repeat expansion carriers. Thus, we have identified one protein component of these pathognomonic inclusions.
Texto completo:
1
Bases de datos:
MEDLINE
Asunto principal:
Secuencias Repetitivas de Ácidos Nucleicos
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Proteínas
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Cuerpos de Inclusión
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Ribonucleoproteína Heterogénea-Nuclear Grupo A-B
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Proteínas Adaptadoras Transductoras de Señales
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Degeneración Lobar Frontotemporal
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Hipocampo
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Esclerosis Amiotrófica Lateral
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Mutación
Tipo de estudio:
Prognostic_studies
Límite:
Humans
Idioma:
En
Revista:
Acta Neuropathol
Año:
2013
Tipo del documento:
Article
País de afiliación:
Alemania