Literature DB >> 23629807

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

Kenji Jinnai1, Maki Mitani, Naonobu Futamura, Kunihiko Kawamoto, Itaru Funakawa, Kyoko Itoh.   

Abstract

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.
Copyright © 2012 Wiley Periodicals, Inc.

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Mesh:

Year:  2013        PMID: 23629807     DOI: 10.1002/mus.23717

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  13 in total

1.  Allele length of the DMPK CTG repeat is a predictor of progressive myotonic dystrophy type 1 phenotypes.

Authors:  Gayle Overend; Cécilia Légaré; Jean Mathieu; Luigi Bouchard; Cynthia Gagnon; Darren G Monckton
Journal:  Hum Mol Genet       Date:  2019-07-01       Impact factor: 6.150

2.  Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study.

Authors:  Marka van Blitterswijk; Mariely DeJesus-Hernandez; Ellis Niemantsverdriet; Melissa E Murray; Michael G Heckman; Nancy N Diehl; Patricia H Brown; Matthew C Baker; NiCole A Finch; Peter O Bauer; Geidy Serrano; Thomas G Beach; Keith A Josephs; David S Knopman; Ronald C Petersen; Bradley F Boeve; Neill R Graff-Radford; Kevin B Boylan; Leonard Petrucelli; Dennis W Dickson; Rosa Rademakers
Journal:  Lancet Neurol       Date:  2013-09-05       Impact factor: 44.182

Review 3.  Modifiers of CAG/CTG Repeat Instability: Insights from Mammalian Models.

Authors:  Vanessa C Wheeler; Vincent Dion
Journal:  J Huntingtons Dis       Date:  2021

4.  Brain MRI abnormalities in the adult form of myotonic dystrophy type 1: A longitudinal case series study.

Authors:  Renata Conforti; Mario de Cristofaro; Adriana Cristofano; Barbara Brogna; Angela Sardaro; Gioacchino Tedeschi; Sossio Cirillo; Alfonso Di Costanzo
Journal:  Neuroradiol J       Date:  2016-01-11

5.  Increased EEG Theta Spectral Power in Sleep in Myotonic Dystrophy Type 1.

Authors:  Joseph Cheung; Chad Ruoff; Hyatt Moore; Katharine A Hagerman; Jennifer Perez; Sarada Sakamuri; Simon C Warby; Emmanuel Mignot; John Day; Jacinda Sampson
Journal:  J Clin Sleep Med       Date:  2018-02-15       Impact factor: 4.062

6.  De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1.

Authors:  Sarah A Cumming; Mark J Hamilton; Yvonne Robb; Helen Gregory; Catherine McWilliam; Anneli Cooper; Berit Adam; Josephine McGhie; Graham Hamilton; Pawel Herzyk; Michael R Tschannen; Elizabeth Worthey; Richard Petty; Bob Ballantyne; Jon Warner; Maria Elena Farrugia; Cheryl Longman; Darren G Monckton
Journal:  Eur J Hum Genet       Date:  2018-07-02       Impact factor: 4.246

7.  Functional impairment in patients with myotonic dystrophy type 1 can be assessed by an ataxia rating scale (SARA).

Authors:  Giovanni DiPaolo; Cecilia Jimenez-Moreno; Nikoletta Nikolenko; Antonio Atalaia; Darren G Monckton; Michela Guglieri; Hanns Lochmüller
Journal:  J Neurol       Date:  2017-02-06       Impact factor: 4.849

8.  Differences in splicing defects between the grey and white matter in myotonic dystrophy type 1 patients.

Authors:  Masamitsu Nishi; Takashi Kimura; Masataka Igeta; Mitsuru Furuta; Koichi Suenaga; Tsuyoshi Matsumura; Harutoshi Fujimura; Kenji Jinnai; Hiroo Yoshikawa
Journal:  PLoS One       Date:  2020-05-14       Impact factor: 3.240

9.  Genetic determinants of disease severity in the myotonic dystrophy type 1 OPTIMISTIC cohort.

Authors:  Sarah A Cumming; Cecilia Jimenez-Moreno; Kees Okkersen; Stephan Wenninger; Ferroudja Daidj; Fiona Hogarth; Roberta Littleford; Gráinne Gorman; Guillaume Bassez; Benedikt Schoser; Hanns Lochmüller; Baziel G M van Engelen; Darren G Monckton
Journal:  Neurology       Date:  2019-08-08       Impact factor: 9.910

10.  Variant repeats within the DMPK CTG expansion protect function in myotonic dystrophy type 1.

Authors:  Jacob N Miller; Ellen van der Plas; Mark Hamilton; Timothy R Koscik; Laurie Gutmann; Sarah A Cumming; Darren G Monckton; Peggy C Nopoulos
Journal:  Neurol Genet       Date:  2020-08-12
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