Literature DB >> 8544186

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

A López de Munain1, A M Cobo, J J Poza, D Navarrete, L Martorell, F Palau, J I Emparanza, M Baiget.   

Abstract

To analyse the influence of the sex of the transmitting grandparents on the occurrence of the congenital form of myotonic dystrophy (CDM), we have studied complete three generation pedigrees of 49 CDM cases, analysing: (1) the sex distribution in the grandparents' generation, and (2) the intergenerational amplification of the CTG repeat, measured in its absolute and relative values, between grandparents and the mothers of CDM patients and between the latter and their CDM children. The mean relative intergenerational increase in the 32 grandparent-mother pairs was significantly greater than in the 56 mother-CDM pairs (Mann-Whitney U test, p < 0.001). The mean expansion of the grandfathers (103 CTG repeats) was also significantly different from that seen in the grandmothers' group (154 CTG repeats) (Mann-Whitney U test, p < 0.01). This excess of non-manifesting males between the CDM grandparents' generation with a smaller CTG length than the grandmothers could suggest that the premutation has to be transmitted by a male to reach the degree of instability responsible for subsequent intergenerational CTG expansions without size constraints characteristic of the CDM range.

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Year:  1995        PMID: 8544186      PMCID: PMC1051667          DOI: 10.1136/jmg.32.9.689

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  23 in total

1.  Explanation for exclusive maternal origin for congenital form of myotonic dystrophy.

Authors:  J C Mulley; A Staples; A Donnelly; A K Gedeon; B K Hecht; G A Nicholson; E A Haan; G R Sutherland
Journal:  Lancet       Date:  1993-01-23       Impact factor: 79.321

2.  Sex-related difference in intergenerational expansion of myotonic dystrophy gene.

Authors:  A M Cobo; M Baiget; A López de Munain; J J Poza; J I Emparanza; K Johnson
Journal:  Lancet       Date:  1993-05-01       Impact factor: 79.321

3.  Structure and genomic sequence of the myotonic dystrophy (DM kinase) gene.

Authors:  M S Mahadevan; C Amemiya; G Jansen; L Sabourin; S Baird; C E Neville; N Wormskamp; B Segers; M Batzer; J Lamerdin
Journal:  Hum Mol Genet       Date:  1993-03       Impact factor: 6.150

4.  Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.

Authors:  M Mahadevan; C Tsilfidis; L Sabourin; G Shutler; C Amemiya; G Jansen; C Neville; M Narang; J Barceló; K O'Hoy
Journal:  Science       Date:  1992-03-06       Impact factor: 47.728

5.  Myotonic dystrophy: size- and sex-dependent dynamics of CTG meiotic instability, and somatic mosaicism.

Authors:  C Lavedan; H Hofmann-Radvanyi; P Shelbourne; J P Rabes; C Duros; D Savoy; I Dehaupas; S Luce; K Johnson; C Junien
Journal:  Am J Hum Genet       Date:  1993-05       Impact factor: 11.025

6.  Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring.

Authors:  J B Redman; R G Fenwick; Y H Fu; A Pizzuti; C T Caskey
Journal:  JAMA       Date:  1993-04-21       Impact factor: 56.272

7.  Different sex-dependent constraints in CTG length variation as explanation for congenital myotonic dystrophy.

Authors:  C Lavedan; H Hofmann-Radvanyi; J P Rabes; J Roume; C Junien
Journal:  Lancet       Date:  1993-01-23       Impact factor: 79.321

8.  Intergenerational stability of the myotonic dystrophy protomutation.

Authors:  J M Barceló; M S Mahadevan; C Tsilfidis; A E MacKenzie; R G Korneluk
Journal:  Hum Mol Genet       Date:  1993-06       Impact factor: 6.150

9.  Cloning of the essential myotonic dystrophy region and mapping of the putative defect.

Authors:  C Aslanidis; G Jansen; C Amemiya; G Shutler; M Mahadevan; C Tsilfidis; C Chen; J Alleman; N G Wormskamp; M Vooijs
Journal:  Nature       Date:  1992-02-06       Impact factor: 49.962

10.  Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy.

Authors:  H G Harley; S A Rundle; J C MacMillan; J Myring; J D Brook; S Crow; W Reardon; I Fenton; D J Shaw; P S Harper
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

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  6 in total

1.  Frequency of myotonic dystrophy gene carriers in cataract patients.

Authors:  A M Cobo; J J Poza; A Blanco; A López de Munain; A Saénz; M Azpitarte; J Marchessi; J F Martí Massó
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

2.  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

3.  Long CTG tracts from the myotonic dystrophy gene induce deletions and rearrangements during recombination at the APRT locus in CHO cells.

Authors:  James L Meservy; R Geoffrey Sargent; Ravi R Iyer; Fung Chan; Gregory J McKenzie; Robert D Wells; John H Wilson
Journal:  Mol Cell Biol       Date:  2003-05       Impact factor: 4.272

4.  CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy.

Authors:  Lise Barbé; Stella Lanni; Arturo López-Castel; Silvie Franck; Claudia Spits; Kathelijn Keymolen; Sara Seneca; Stephanie Tomé; Ioana Miron; Julie Letourneau; Minggao Liang; Sanaa Choufani; Rosanna Weksberg; Michael D Wilson; Zdenek Sedlacek; Cynthia Gagnon; Zuzana Musova; David Chitayat; Patrick Shannon; Jean Mathieu; Karen Sermon; Christopher E Pearson
Journal:  Am J Hum Genet       Date:  2017-03-02       Impact factor: 11.025

Review 5.  DM1 Phenotype Variability and Triplet Repeat Instability: Challenges in the Development of New Therapies.

Authors:  Stéphanie Tomé; Geneviève Gourdon
Journal:  Int J Mol Sci       Date:  2020-01-10       Impact factor: 5.923

6.  DMPK hypermethylation in sperm cells of myotonic dystrophy type 1 patients.

Authors:  Shira Yanovsky-Dagan; Eliora Cohen; Pauline Megalli; Gheona Altarescu; Oshrat Schonberger; Talia Eldar-Geva; Silvina Epsztejn-Litman; Rachel Eiges
Journal:  Eur J Hum Genet       Date:  2021-11-15       Impact factor: 5.351

  6 in total

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