Literature DB >> 25662336

Age-, tissue- and length-dependent bidirectional somatic CAG•CTG repeat instability in an allelic series of R6/2 Huntington disease mice.

Eloise Larson1, Ian Fyfe2, A Jennifer Morton3, Darren G Monckton4.   

Abstract

The expansion of simple sequence CAG•CTG repeats is associated with a number of inherited disorders including Huntington disease (HD), myotonic dystrophy type 1 and several of the spinocerebellar ataxias. Inherited disease-associated alleles usually exceed 40 repeats and may be in excess of 1,000 repeats in some disorders. Inherited allele length is inversely proportional to age at onset, and frequent germline expansions account for the striking anticipation observed in affected families. Expanded disease associated alleles are also somatically unstable via a pathway that is age dependent and tissue specific, and also appears to be expansion biased. Somatic expansions are thought to contribute toward both tissue specificity and disease progression. Here we have examined the somatic mutational dynamics in brain and peripheral tissues from an allelic series of R6/2 HD transgenic mice inheriting from 52 to >700 CAG repeats. We found age-dependent, tissue-specific somatic instability, with particularly large expansions observed in the striatum and cortex. We also found a positive increase in somatic instability with increasing allele length. Surprisingly, however, the degree of somatic variation did not increase in a linear fashion, but leveled off with increasing allele length. Most unexpectedly, the almost exclusive bias toward the accumulation of expansions observed in mice inheriting smaller alleles was lost, and a high frequency of large somatic contractions was observed in mice inheriting very large alleles (>500 repeats). These data highlight the bidirectional nature of CAG•CTG repeat instability and the subtle balance that exists between expansion and contraction in vivo. Defining the dynamics and tissue specificity of expansion and contraction is important for understanding the role of genetic instability in pathophysiology and in particular the development of novel therapies based on suppressing expansions and/or promoting contractions.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Huntington disease (HD); Mutation; Polyglutamine expansion; R6/2 mice; Somatic instability; Trinucleotide repeat expansion

Mesh:

Year:  2015        PMID: 25662336     DOI: 10.1016/j.nbd.2015.01.004

Source DB:  PubMed          Journal:  Neurobiol Dis        ISSN: 0969-9961            Impact factor:   5.996


  16 in total

Review 1.  Modifiers of CAG/CTG Repeat Instability: Insights from Mammalian Models.

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

2.  Ophthalmic features of spinocerebellar ataxia type 7.

Authors:  A Campos-Romo; E O Graue-Hernandez; L Pedro-Aguilar; J C Hernandez-Camarena; D Rivera-De la Parra; V Galvez; R Diaz; A Jimenez-Corona; J Fernandez-Ruiz
Journal:  Eye (Lond)       Date:  2017-08-11       Impact factor: 3.775

3.  Propensity for somatic expansion increases over the course of life in Huntington disease.

Authors:  Radhia Kacher; François-Xavier Lejeune; Sandrine Noël; Cécile Cazeneuve; Alexis Brice; Sandrine Humbert; Alexandra Durr
Journal:  Elife       Date:  2021-05-13       Impact factor: 8.140

4.  The pathogenic exon 1 HTT protein is produced by incomplete splicing in Huntington's disease patients.

Authors:  Andreas Neueder; Christian Landles; Rhia Ghosh; David Howland; Richard H Myers; Richard L M Faull; Sarah J Tabrizi; Gillian P Bates
Journal:  Sci Rep       Date:  2017-05-02       Impact factor: 4.379

5.  Analysis of mutational dynamics at the DMPK (CTG)n locus identifies saliva as a suitable DNA sample source for genetic analysis in myotonic dystrophy type 1.

Authors:  Eyleen Corrales; Melissa Vásquez; Baili Zhang; Carolina Santamaría-Ulloa; Patricia Cuenca; Ralf Krahe; Darren G Monckton; Fernando Morales
Journal:  PLoS One       Date:  2019-05-02       Impact factor: 3.240

6.  A selective inhibitor of histone deacetylase 3 prevents cognitive deficits and suppresses striatal CAG repeat expansions in Huntington's disease mice.

Authors:  Nuria Suelves; Lucy Kirkham-McCarthy; Robert S Lahue; Silvia Ginés
Journal:  Sci Rep       Date:  2017-07-20       Impact factor: 4.379

7.  XJB-5-131-mediated improvement in physiology and behaviour of the R6/2 mouse model of Huntington's disease is age- and sex- dependent.

Authors:  Aris A Polyzos; Nigel I Wood; Paul Williams; Peter Wipf; A Jennifer Morton; Cynthia T McMurray
Journal:  PLoS One       Date:  2018-04-09       Impact factor: 3.240

8.  Patterns of CAG repeat instability in the central nervous system and periphery in Huntington's disease and in spinocerebellar ataxia type 1.

Authors:  Ricardo Mouro Pinto; Larissa Arning; James V Giordano; Pedram Razghandi; Marissa A Andrew; Tammy Gillis; Kevin Correia; Jayalakshmi S Mysore; Debora-M Grote Urtubey; Constanze R Parwez; Sarah M von Hein; H Brent Clark; Huu Phuc Nguyen; Eckart Förster; Allison Beller; Suman Jayadaev; C Dirk Keene; Thomas D Bird; Diane Lucente; Jean-Paul Vonsattel; Harry Orr; Carsten Saft; Elisabeth Petrasch-Parwez; Vanessa C Wheeler
Journal:  Hum Mol Genet       Date:  2020-08-29       Impact factor: 6.150

9.  A slipped-CAG DNA-binding small molecule induces trinucleotide-repeat contractions in vivo.

Authors:  Masayuki Nakamori; Gagan B Panigrahi; Stella Lanni; Terence Gall-Duncan; Hideki Hayakawa; Hana Tanaka; Jennifer Luo; Takahiro Otabe; Jinxing Li; Akihiro Sakata; Marie-Christine Caron; Niraj Joshi; Tanya Prasolava; Karen Chiang; Jean-Yves Masson; Marc S Wold; Xiaoxiao Wang; Marietta Y W T Lee; John Huddleston; Katherine M Munson; Scott Davidson; Mehdi Layeghifard; Lisa-Monique Edward; Richard Gallon; Mauro Santibanez-Koref; Asako Murata; Masanori P Takahashi; Evan E Eichler; Adam Shlien; Kazuhiko Nakatani; Hideki Mochizuki; Christopher E Pearson
Journal:  Nat Genet       Date:  2020-02-14       Impact factor: 38.330

10.  Relatively semi-conservative replication and a folded slippage model for short tandem repeats.

Authors:  Hongxi Zhang; Douyue Li; Xiangyan Zhao; Saichao Pan; Xiaolong Wu; Shan Peng; Hanrou Huang; Ruixue Shi; Zhongyang Tan
Journal:  BMC Genomics       Date:  2020-08-17       Impact factor: 3.969

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