Literature DB >> 18286225

Segregation distortion of wild-type alleles at the Machado-Joseph disease locus: a study in normal families from the Azores islands (Portugal).

Conceição Bettencourt1, Raquel Nunes Fialho2,3, Cristina Santos4, Rafael Montiel4, Jácome Bruges-Armas2,3, Patrícia Maciel5, Manuela Lima4.   

Abstract

Machado-Joseph disease (MJD) is caused by an expansion of a triplet repeat with a CAG motif at the ATXN3 gene. The putative segregation ratio distortion (SRD) of alleles can play an important role in the non-Mendelian behaviour of triplet repeat loci. To study the stability and infer the segregation patterns of wild-type MJD alleles, the size of the (CAG)(n) tract was analysed in 102 normal sibships, representing 428 meioses. No mutational events were detected during the transmission of alleles. Segregation analysis showed that the smaller alleles were preferentially transmitted (56.9%). Considering maternal meioses alone, such preference was still detected (55.7%) but without statistical significance. A positive correlation was observed for the difference in length between the two alleles constituting the transmitters' genotype (D) and the frequency of transmission of the smaller alleles. The results suggest that small D values are not enough to modify the probability of allele transmission. When transmissions involving genotypes with D <or= 2 were excluded, SRD in favour of the smaller allele became significant for both maternal and paternal transmissions. Therefore, the genotypic composition of the transmitters in a sample to be analysed should influence the ability to detect SRD, acting as a confounding factor.

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Year:  2008        PMID: 18286225     DOI: 10.1007/s10038-008-0261-7

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  32 in total

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Authors:  H Ellegren
Journal:  Trends Genet       Date:  2000-12       Impact factor: 11.639

2.  Non-Mendelian transmission at the Machado-Joseph disease locus in normal females: preferential transmission of alleles with smaller CAG repeats.

Authors:  D C Rubinsztein; J Leggo
Journal:  J Med Genet       Date:  1997-03       Impact factor: 6.318

Review 3.  Dynamic mutations: a new class of mutations causing human disease.

Authors:  R I Richards; G R Sutherland
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4.  Improved single-strand DNA sizing accuracy in capillary electrophoresis.

Authors:  B B Rosenblum; F Oaks; S Menchen; B Johnson
Journal:  Nucleic Acids Res       Date:  1997-10-01       Impact factor: 16.971

5.  Diagnosis of five spinocerebellar ataxia disorders by multiplex amplification and capillary electrophoresis.

Authors:  Michael O Dorschner; Deborah Barden; Karen Stephens
Journal:  J Mol Diagn       Date:  2002-05       Impact factor: 5.568

6.  French Machado-Joseph disease patients do not exhibit gametic segregation distortion: a sperm typing analysis.

Authors:  R P Grewal; G Cancel; E P Leeflang; A Dürr; M S McPeek; D Draghinas; X Yao; G Stevanin; M O Alnot; A Brice; N Arnheim
Journal:  Hum Mol Genet       Date:  1999-09       Impact factor: 6.150

7.  De novo expansion of intermediate alleles in spinocerebellar ataxia 7.

Authors:  G Stevanin; P Giunti; G D Belal; A Dürr; M Ruberg; N Wood; A Brice
Journal:  Hum Mol Genet       Date:  1998-10       Impact factor: 6.150

8.  Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease.

Authors:  Y Takiyama; S Igarashi; E A Rogaeva; K Endo; E I Rogaev; H Tanaka; R Sherrington; K Sanpei; Y Liang; M Saito
Journal:  Hum Mol Genet       Date:  1995-07       Impact factor: 6.150

9.  Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations.

Authors:  H Takano; G Cancel; T Ikeuchi; D Lorenzetti; R Mawad; G Stevanin; O Didierjean; A Dürr; M Oyake; T Shimohata; R Sasaki; R Koide; S Igarashi; S Hayashi; Y Takiyama; M Nishizawa; H Tanaka; H Zoghbi; A Brice; S Tsuji
Journal:  Am J Hum Genet       Date:  1998-10       Impact factor: 11.025

10.  Meiotic drive at the myotonic dystrophy locus.

Authors:  M Gennarelli; B Dallapiccola; M Baiget; L Martorell; G Novelli
Journal:  J Med Genet       Date:  1994-12       Impact factor: 6.318

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  11 in total

Review 1.  Machado-Joseph Disease: from first descriptions to new perspectives.

Authors:  Conceição Bettencourt; Manuela Lima
Journal:  Orphanet J Rare Dis       Date:  2011-06-02       Impact factor: 4.123

2.  Sequence analysis of 5' regulatory regions of the Machado-Joseph disease gene (ATXN3).

Authors:  Conceição Bettencourt; Mafalda Raposo; Nadiya Kazachkova; Cristina Santos; Teresa Kay; João Vasconcelos; Patrícia Maciel; Karina C Donis; Maria Luiza Saraiva-Pereira; Laura B Jardim; Jorge Sequeiros; Jácome Bruges-Armas; Manuela Lima
Journal:  Cerebellum       Date:  2012-12       Impact factor: 3.847

3.  Promoter Variation and Expression Levels of Inflammatory Genes IL1A, IL1B, IL6 and TNF in Blood of Spinocerebellar Ataxia Type 3 (SCA3) Patients.

Authors:  Mafalda Raposo; Conceição Bettencourt; Amanda Ramos; Nadiya Kazachkova; João Vasconcelos; Teresa Kay; Jácome Bruges-Armas; Manuela Lima
Journal:  Neuromolecular Med       Date:  2016-05-31       Impact factor: 3.843

4.  Promoter Variant Alters Expression of the Autophagic BECN1 Gene: Implications for Clinical Manifestations of Machado-Joseph Disease.

Authors:  Nadiya Kazachkova; Mafalda Raposo; Amanda Ramos; Rafael Montiel; Manuela Lima
Journal:  Cerebellum       Date:  2017-12       Impact factor: 3.847

5.  Triplet Repeat Primed PCR (TP-PCR) in Molecular Diagnostic Testing for Spinocerebellar Ataxia Type 3 (SCA3).

Authors:  Ana Rosa Vieira Melo; Amanda Ramos; Nadiya Kazachkova; Mafalda Raposo; Bruno Filipe Bettencourt; Ana Rita Rendeiro; Teresa Kay; João Vasconcelos; Jácome Bruges-Armas; Manuela Lima
Journal:  Mol Diagn Ther       Date:  2016-12       Impact factor: 4.074

6.  Genetic Variation in ATXN3 (Ataxin-3) 3'UTR: Insights into the Downstream Regulatory Elements of the Causative Gene of Machado-Joseph Disease/Spinocerebellar Ataxia Type 3.

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Journal:  Cerebellum       Date:  2022-01-16       Impact factor: 3.847

Review 7.  Transmission ratio distortion: review of concept and implications for genetic association studies.

Authors:  Lam Opal Huang; Aurélie Labbe; Claire Infante-Rivard
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8.  The (CAG)n tract of Machado-Joseph Disease gene (ATXN3): a comparison between DNA and mRNA in patients and controls.

Authors:  Conceição Bettencourt; Cristina Santos; Rafael Montiel; Teresa Kay; João Vasconcelos; Patrícia Maciel; Manuela Lima
Journal:  Eur J Hum Genet       Date:  2009-11-25       Impact factor: 4.246

9.  Analysis of segregation patterns in Machado-Joseph disease pedigrees.

Authors:  Conceição Bettencourt; Cristina Santos; Teresa Kay; João Vasconcelos; Manuela Lima
Journal:  J Hum Genet       Date:  2008-08-09       Impact factor: 3.172

10.  Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): a two-case report.

Authors:  Conceição Bettencourt; Cristina Santos; Paula Coutinho; Patrizia Rizzu; João Vasconcelos; Teresa Kay; Teresa Cymbron; Mafalda Raposo; Peter Heutink; Manuela Lima
Journal:  BMC Neurol       Date:  2011-10-24       Impact factor: 2.474

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