Literature DB >> 8116611

Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy.

T Ashizawa1, M Anvret, M Baiget, J M Barceló, H Brunner, A M Cobo, B Dallapiccola, R G Fenwick, U Grandell, H Harley.   

Abstract

In myotonic dystrophy (DM), the size of a CTG repeat in the DM kinase gene generally increases in successive generations with clinical evidence of anticipation. However, there have also been cases with an intergenerational contraction of the repeat. We examined 1,489 DM parent-offspring pairs, of which 95 (6.4%) showed such contractions in peripheral blood leukocytes (PBL). In 56 of the 95 pairs, clinical data allowed an analysis of their anticipation status. It is surprising that anticipation occurred in 27 (48%) of these 56 pairs, while none clearly showed a later onset of DM in the symptomatic offspring. The contraction occurred in 76 (10%) of 753 paternal transmissions and in 19 (3%) of 736 maternal transmissions. Anticipation was observed more frequently in maternal (85%) than in paternal (37%) transmissions (P < .001). The parental repeat size correlated with the size of intergenerational contraction (r2 = .50, P << .001), and the slope of linear regression was steeper in paternal (-.62) than in maternal (-.30) transmissions (P << .001). Sixteen DM parents had multiple DM offspring with the CTG repeat contractions. This frequency was higher than the frequency expected from the probability of the repeat contractions (6.4%) and the size of DM sib population (1.54 DM offspring per DM parent, in 968 DM parents). We conclude that (1) intergenerational contractions of the CTG repeat in leukocyte DNA frequently accompanies apparent anticipation, especially when DM is maternally transmitted, and (2) the paternal origin of the repeat and the presence of the repeat contraction in a sibling increase the probability of the CTG repeat contraction.

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Year:  1994        PMID: 8116611      PMCID: PMC1918128     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  38 in total

1.  Genetic risks for children of women with myotonic dystrophy.

Authors:  M C Koch; T Grimm; H G Harley; P S Harper
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

2.  Effects of the sex of myotonic dystrophy patients on the unstable triplet repeat in their affected offspring.

Authors:  T Ashizawa; P W Dunne; P A Ward; W K Seltzer; C S Richards
Journal:  Neurology       Date:  1994-01       Impact factor: 9.910

3.  No imprinting involved in the expression of DM-kinase mRNAs in mouse and human tissues.

Authors:  G Jansen; M Bartolomei; V Kalscheuer; G Merkx; N Wormskamp; E Mariman; D Smeets; H H Ropers; B Wieringa
Journal:  Hum Mol Genet       Date:  1993-08       Impact factor: 6.150

4.  Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM).

Authors:  H G Brunner; H T Brüggenwirth; W Nillesen; G Jansen; B C Hamel; R L Hoppe; C E de Die; C J Höweler; B A van Oost; B Wieringa
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

5.  Myotonic dystrophy: absence of CTG enlarged transcript in congenital forms, and low expression of the normal allele.

Authors:  H Hofmann-Radvanyi; C Lavedan; J P Rabès; D Savoy; C Duros; K Johnson; C Junien
Journal:  Hum Mol Genet       Date:  1993-08       Impact factor: 6.150

6.  Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene.

Authors:  L A Sabouri; M S Mahadevan; M Narang; D S Lee; L C Surh; R G Korneluk
Journal:  Nat Genet       Date:  1993-07       Impact factor: 38.330

7.  Somatic instability of CTG repeat in myotonic dystrophy.

Authors:  T Ashizawa; J R Dubel; Y Harati
Journal:  Neurology       Date:  1993-12       Impact factor: 9.910

8.  Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype.

Authors:  P Shelbourne; R Winqvist; E Kunert; J Davies; J Leisti; H Thiele; H Bachmann; J Buxton; B Williamson; K Johnson
Journal:  Hum Mol Genet       Date:  1992-10       Impact factor: 6.150

9.  Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

Authors:  J D Brook; M E McCurrach; H G Harley; A J Buckler; D Church; H Aburatani; K Hunter; V P Stanton; J P Thirion; T Hudson
Journal:  Cell       Date:  1992-02-21       Impact factor: 41.582

10.  Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy.

Authors:  M Anvret; G Ahlberg; U Grandell; B Hedberg; K Johnson; L Edström
Journal:  Hum Mol Genet       Date:  1993-09       Impact factor: 6.150

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  38 in total

1.  Segregation distortion of the CTG repeats at the myotonic dystrophy locus.

Authors:  R Chakraborty; D N Stivers; R Deka; L M Yu; M D Shriver; R E Ferrell
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

2.  Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues.

Authors:  Arturo López Castel; Masayuki Nakamori; Stephanie Tomé; David Chitayat; Geneviève Gourdon; Charles A Thornton; Christopher E Pearson
Journal:  Hum Mol Genet       Date:  2010-11-01       Impact factor: 6.150

3.  Decrease in the CGGn trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmission.

Authors:  M L Väisänen; R Haataja; J Leisti
Journal:  Am J Hum Genet       Date:  1996-09       Impact factor: 11.025

Review 4.  Myotonic dystrophy.

Authors:  Charles A Thornton
Journal:  Neurol Clin       Date:  2014-06-06       Impact factor: 3.806

5.  Instability of TCF4 Triplet Repeat Expansion With Parent-Child Transmission in Fuchs' Endothelial Corneal Dystrophy.

Authors:  Joanna S Saade; Chao Xing; Xin Gong; Zhengyang Zhou; V Vinod Mootha
Journal:  Invest Ophthalmol Vis Sci       Date:  2018-08-01       Impact factor: 4.799

6.  Absence of MutSβ leads to the formation of slipped-DNA for CTG/CAG contractions at primate replication forks.

Authors:  Meghan M Slean; Gagan B Panigrahi; Arturo López Castel; August B Pearson; Alan E Tomkinson; Christopher E Pearson
Journal:  DNA Repair (Amst)       Date:  2016-04-16

Review 7.  Myotonic dystrophy: disease repeat range, penetrance, age of onset, and relationship between repeat size and phenotypes.

Authors:  Kevin Yum; Eric T Wang; Auinash Kalsotra
Journal:  Curr Opin Genet Dev       Date:  2017-02-14       Impact factor: 5.578

8.  Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions.

Authors:  Jovan Pešović; S Perić; M Brkušanin; G Brajušković; V Rakočević-Stojanović; Dušanka Savić-Pavićević
Journal:  Neurogenetics       Date:  2017-09-23       Impact factor: 2.660

9.  Direct molecular analysis of myotonic dystrophy in the German population: important considerations in genetic counselling.

Authors:  A Meiner; C Wolf; N Carey; A Okitsu; K Johnson; P Shelbourne; B Kunath; W Sauermann; H Thiele; P Kupferling
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

10.  Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability.

Authors:  Karen N McFarland; Jilin Liu; Ivette Landrian; Rui Gao; Partha S Sarkar; Salmo Raskin; Mariana Moscovich; Emilia M Gatto; Hélio A G Teive; Adriana Ochoa; Astrid Rasmussen; Tetsuo Ashizawa
Journal:  Eur J Hum Genet       Date:  2013-02-27       Impact factor: 4.246

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