Literature DB >> 7825583

Mapping of the gene for Machado-Joseph disease within a 3.6-cM interval flanked by D14S291/D14S280 and D14S81, on the basis of studies of linkage and linkage disequilibrium in 24 Japanese families.

H Sasaki1, A Wakisaka, A Takada, T Yoshiki, T Ihara, Y Suzuki, T Hamada, K Iwabuchi, K Onari, J Tada.   

Abstract

The gene locus of Machado-Joseph disease (MJD) has recently been mapped within a 29-cM subregion of 14q chromosome. We did a linkage study of 24 multigenerational MJD Japanese pedigrees, in an attempt to narrow the candidate region of this gene. Pairwise and multipoint linkage analysis, together with haplotype segregation analysis, led to the conclusion that the MJD gene is located at the 6.8-cM interval between D14S256 and D14S81 (Zmax = 24.78, multipoint linkage analysis). D14S291 and D14S280, located at the center of this interval, showed no obligate recombination with the MJD gene (Zmax = 5.93 for D14S291 and 9.99 for D14S280). A weak, but significant, linkage disequilibrium of MJD gene was noted with D14S81 (P < .05) but not with D14S291 or D14S280. These results suggest that a 3.6-cM interval flanked by D14S291/D14S280 and D14S81 is the most likely location of the MJD gene and that it is closest to D14S81.

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Year:  1995        PMID: 7825583      PMCID: PMC1801343     

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


  32 in total

1.  Machado disease. A hereditary ataxia in Portuguese emigrants to Massachusetts.

Authors:  K K Nakano; D M Dawson; A Spence
Journal:  Neurology       Date:  1972-01       Impact factor: 9.910

2.  Anticipation in spinocerebellar ataxia type 2.

Authors:  S M Pulst; A Nechiporuk; S Starkman
Journal:  Nat Genet       Date:  1993-09       Impact factor: 38.330

3.  Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p.

Authors:  L P Ranum; L A Duvick; S S Rich; L J Schut; M Litt; H T Orr
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

4.  [Linkage study of Machado-Joseph disease: genetic evidence for the locus different from SCA1].

Authors:  H Sasaki; A Wakisaka; K Tashiro; T Hamada; T Katoh
Journal:  Rinsho Shinkeigaku       Date:  1992-01

5.  Mapping, cloning and genetic characterization of the region containing the Wilson disease gene.

Authors:  K Petrukhin; S G Fischer; M Pirastu; R E Tanzi; I Chernov; M Devoto; L M Brzustowicz; E Cayanis; E Vitale; J J Russo
Journal:  Nat Genet       Date:  1993-12       Impact factor: 38.330

6.  A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus.

Authors:  G Stevanin; E Le Guern; N Ravisé; H Chneiweiss; A Dürr; G Cancel; A Vignal; A L Boch; M Ruberg; C Penet
Journal:  Am J Hum Genet       Date:  1994-01       Impact factor: 11.025

7.  Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

Authors:  M Y Chung; L P Ranum; L A Duvick; A Servadio; H Y Zoghbi; H T Orr
Journal:  Nat Genet       Date:  1993-11       Impact factor: 38.330

8.  Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1.

Authors:  S Gispert; R Twells; G Orozco; A Brice; J Weber; L Heredero; K Scheufler; B Riley; R Allotey; C Nothers
Journal:  Nat Genet       Date:  1993-07       Impact factor: 38.330

9.  The gene for Machado-Joseph disease maps to human chromosome 14q.

Authors:  Y Takiyama; M Nishizawa; H Tanaka; S Kawashima; H Sakamoto; Y Karube; H Shimazaki; M Soutome; K Endo; S Ohta
Journal:  Nat Genet       Date:  1993-07       Impact factor: 38.330

10.  Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p.

Authors:  S Nagafuchi; H Yanagisawa; K Sato; T Shirayama; E Ohsaki; M Bundo; T Takeda; K Tadokoro; I Kondo; N Murayama
Journal:  Nat Genet       Date:  1994-01       Impact factor: 38.330

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  4 in total

1.  The placenta growth factor gene of the mouse.

Authors:  T DiPalma; M Tucci; G Russo; D Maglione; C T Lago; A Romano; S Saccone; G Della Valle; L De Gregorio; T A Dragani; G Viglietto; M G Persico
Journal:  Mamm Genome       Date:  1996-01       Impact factor: 2.957

2.  Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph disease.

Authors:  G Stevanin; E Cassa; G Cancel; N Abbas; A Dürr; E Jardim; Y Agid; P S Sousa; A Brice
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

3.  Spinocerebellar ataxia 1 (SCA1) in the Japanese in Hokkaido may derive from a single common ancestry.

Authors:  A Wakisaka; H Sasaki; A Takada; T Fukazawa; Y Suzuki; T Hamada; K Iwabuchi; K Tashiro; T Yoshiki
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

4.  Molecular analysis of three patients with interstitial deletions of chromosome band 14q31.

Authors:  B C Byth; M T Costa; I E Teshima; W G Wilson; N P Carter; D W Cox
Journal:  J Med Genet       Date:  1995-07       Impact factor: 6.318

  4 in total

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