Literature DB >> 8290046

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

T Ashizawa1, P W Dunne, P A Ward, W K Seltzer, C S Richards.   

Abstract

The mutation responsible for myotonic dystrophy (DM) is an unstable expansion of the CTG repeat within the myotonin protein kinase gene. To examine whether the parental origin of the expanded repeat influences the repeat size in offspring, we studied 51 father-child and 59 mother-child pairs with DM. Small expansions in fathers resulted in larger size expansions in their offspring, while large paternal expansions resulted in less size change in their offspring. However, there was no correlation between maternal size expansion and size increase in offspring for either congenital or noncongenital DM. These data suggest that the sex of the affected parent influences the unstable expansion of the repeat in DM offspring. While some evidence suggests that DNA methylation status cannot explain this observation, the mechanism for differential maternal/paternal transmission expansion is currently unknown.

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Year:  1994        PMID: 8290046     DOI: 10.1212/wnl.44.1.120

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  15 in total

1.  FMR1 CGG-repeat instability in single sperm and lymphocytes of fragile-X premutation males.

Authors:  S L Nolin; G E Houck; A D Gargano; H Blumstein; C S Dobkin; W T Brown
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

Review 2.  Anticipation and CAG*CTG repeat expansion in schizophrenia and bipolar affective disorder.

Authors:  M Teresa Fortune; James L Kennedy; John B Vincent
Journal:  Curr Psychiatry Rep       Date:  2003-06       Impact factor: 5.285

3.  Instability of the (CTG)n repeat in congenital myotonic dystrophy.

Authors:  L J Wong; T Ashizawa
Journal:  Am J Hum Genet       Date:  1997-12       Impact factor: 11.025

4.  Paternal transmission of congenital myotonic dystrophy.

Authors:  C E de Die-Smulders; H J Smeets; W Loots; H B Anten; J F Mirandolle; J P Geraedts; C J Höweler
Journal:  J Med Genet       Date:  1997-11       Impact factor: 6.318

5.  CTG repeat instability and size variation timing in DNA repair-deficient mice.

Authors:  Cédric Savouret; Edith Brisson; Jeroen Essers; Roland Kanaar; Albert Pastink; Hein te Riele; Claudine Junien; Geneviève Gourdon
Journal:  EMBO J       Date:  2003-05-01       Impact factor: 11.598

6.  Parental age effects, but no evidence for an intrauterine effect in the transmission of myotonic dystrophy type 1.

Authors:  Fernando Morales; Melissa Vásquez; Patricia Cuenca; Domingo Campos; Carolina Santamaría; Gerardo Del Valle; Roberto Brian; Mauricio Sittenfeld; Darren G Monckton
Journal:  Eur J Hum Genet       Date:  2014-07-23       Impact factor: 4.246

7.  Influence of the sex of the transmitting grandparent in congenital myotonic dystrophy.

Authors:  A López de Munain; A M Cobo; J J Poza; D Navarrete; L Martorell; F Palau; J I Emparanza; M Baiget
Journal:  J Med Genet       Date:  1995-09       Impact factor: 6.318

8.  The fragile X premutation in carriers and its effect on mutation size in offspring.

Authors:  G S Fisch; K Snow; S N Thibodeau; M Chalifaux; J J Holden; D L Nelson; P N Howard-Peebles; A Maddalena
Journal:  Am J Hum Genet       Date:  1995-05       Impact factor: 11.025

9.  Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent.

Authors:  L J Wong; T Ashizawa; D G Monckton; C T Caskey; C S Richards
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

10.  Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10.

Authors:  Tohru Matsuura; Ping Fang; Xi Lin; Mehrdad Khajavi; Kuniko Tsuji; Astrid Rasmussen; Raji P Grewal; Madhureeta Achari; Maria E Alonso; Stefan M Pulst; Huda Y Zoghbi; David L Nelson; Benjamin B Roa; Tetsuo Ashizawa
Journal:  Am J Hum Genet       Date:  2004-05-04       Impact factor: 11.025

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