Somatic instability of CTG repeats in the cerebellum of myotonic dystrophy type 1

Introduction: We statistically analyzed somatic instability of the CTG expansion in the central nervous system and visceral organs in 7 patients with myotonic dystrophy type 1 and also report intracerebellar instability in 2 patients. Methods: CTG repeat expansion was estimated in the samples from a...

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Veröffentlicht in:Muscle & nerve 2013-07, Vol.48 (1), p.105-108
Hauptverfasser: Jinnai, Kenji, Mitani, Maki, Futamura, Naonobu, Kawamoto, Kunihiko, Funakawa, Itaru, Itoh, Kyoko
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container_end_page 108
container_issue 1
container_start_page 105
container_title Muscle & nerve
container_volume 48
creator Jinnai, Kenji
Mitani, Maki
Futamura, Naonobu
Kawamoto, Kunihiko
Funakawa, Itaru
Itoh, Kyoko
description Introduction: We statistically analyzed somatic instability of the CTG expansion in the central nervous system and visceral organs in 7 patients with myotonic dystrophy type 1 and also report intracerebellar instability in 2 patients. Methods: CTG repeat expansion was estimated in the samples from autopsied brains and visceral organs by Southern blot analysis. Pathological study was performed. Samples were taken from several sites in the cerebellum to examine intracerebellar instability. Results: The CTG repeat expansion was shortest in the cerebellar cortex among all tissues examined. With regard to the intracerebellar difference, the shortest expansion was seen in the cortices of the hemisphere and vermis, whereas it was moderate in the dentate nucleus and longest in the white matter of the hemisphere and middle cerebellar peduncle. Conclusions: The shortest expansion might be attributable to packed granule cells in the cerebellar cortex. Further analysis of cell‐specific methylation states might elucidate the enigma of somatic instability. Muscle Nerve, 2013
doi_str_mv 10.1002/mus.23717
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Methods: CTG repeat expansion was estimated in the samples from autopsied brains and visceral organs by Southern blot analysis. Pathological study was performed. Samples were taken from several sites in the cerebellum to examine intracerebellar instability. Results: The CTG repeat expansion was shortest in the cerebellar cortex among all tissues examined. With regard to the intracerebellar difference, the shortest expansion was seen in the cortices of the hemisphere and vermis, whereas it was moderate in the dentate nucleus and longest in the white matter of the hemisphere and middle cerebellar peduncle. Conclusions: The shortest expansion might be attributable to packed granule cells in the cerebellar cortex. Further analysis of cell‐specific methylation states might elucidate the enigma of somatic instability. 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Methods: CTG repeat expansion was estimated in the samples from autopsied brains and visceral organs by Southern blot analysis. Pathological study was performed. Samples were taken from several sites in the cerebellum to examine intracerebellar instability. Results: The CTG repeat expansion was shortest in the cerebellar cortex among all tissues examined. With regard to the intracerebellar difference, the shortest expansion was seen in the cortices of the hemisphere and vermis, whereas it was moderate in the dentate nucleus and longest in the white matter of the hemisphere and middle cerebellar peduncle. Conclusions: The shortest expansion might be attributable to packed granule cells in the cerebellar cortex. Further analysis of cell‐specific methylation states might elucidate the enigma of somatic instability. 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subjects Aged
Brain
cerebellum
Cerebellum - pathology
Cerebellum - physiology
CTG repeat
Female
Humans
Male
Middle Aged
Muscular dystrophy
Myotonic Dystrophy - genetics
Myotonic Dystrophy - pathology
myotonic dystrophy type 1
somatic instability
Trinucleotide Repeat Expansion - genetics
title Somatic instability of CTG repeats in the cerebellum of myotonic dystrophy type 1
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