Literature DB >> 8808607

Search for unstable DNA in schizophrenia families with evidence for genetic anticipation.

A Petronis1, A S Bassett, W G Honer, J B Vincent, Y Tatuch, T Sasaki, D J Ying, T A Klempan, J L Kennedy.   

Abstract

Evidence for genetic anticipation has recently become an important subject of research in clinical psychiatric genetics. Renewed interest in anticipation was evoked by molecular genetic findings of a novel type of mutation termed "unstable DNA." The unstable DNA model can be construed as the "best fit" for schizophrenia twin and family epidemiological data. We have performed a large-scale Southern blot hybridization, asymmetrical PCR-based, and repeat expansion-detection screening for (CAG)n/(CTG)n and (CCG)n/(CGG)n expansions in eastern Canadian schizophrenia multiplex families demonstrating genetic anticipation. There were no differences in (CAG)n/(CTG)n and (CCG)n/(CGG)n pattern distribution either between affected and unaffected individuals or across generations. Our findings do not support the hypothesis that large (CAG)n/(CTG)n or (CCG)n/(CGG)n expansions are the major etiologic factor in schizophrenia. A separate set of experiments directed to the analysis of small (30-130 trinucleotides), Huntington disease-type expansions in individual genes is required in order to fully exclude the presence of (CAG)n/(CTG)n- or (CCG)n/(CGG)n-type unstable mutation.

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Year:  1996        PMID: 8808607      PMCID: PMC1914813     

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


  30 in total

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Authors:  R I Richards; G R Sutherland
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2.  Heritable unstable DNA sequences.

Authors:  R I Richards; G R Sutherland
Journal:  Nat Genet       Date:  1992-04       Impact factor: 38.330

Review 3.  Genomic imprinting in hereditary glomus tumours: evidence for new genetic theory.

Authors:  A G van der Mey; P D Maaswinkel-Mooy; C J Cornelisse; P H Schmidt; J J van de Kamp
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Review 4.  Triplet repeat mutations in human disease.

Authors:  C T Caskey; A Pizzuti; Y H Fu; R G Fenwick; D L Nelson
Journal:  Science       Date:  1992-05-08       Impact factor: 47.728

5.  Detection of expanded CAG repeats in bipolar affective disorder using the repeat expansion detection (RED) method.

Authors:  K Lindblad; P O Nylander; A De bruyn; D Sourey; C Zander; C Engström; G Holmgren; T Hudson; J Chotai; J Mendlewicz
Journal:  Neurobiol Dis       Date:  1995-02       Impact factor: 5.996

6.  Anticipation in bipolar affective disorder.

Authors:  M G McInnis; F J McMahon; G A Chase; S G Simpson; C A Ross; J R DePaulo
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

7.  Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms.

Authors:  S H Li; M G McInnis; R L Margolis; S E Antonarakis; C A Ross
Journal:  Genomics       Date:  1993-06       Impact factor: 5.736

8.  Analysis of a large kindred with Blau syndrome for HLA, autoimmunity, and sarcoidosis.

Authors:  S A Raphael; E B Blau; W H Zhang; S H Hsu
Journal:  Am J Dis Child       Date:  1993-08

9.  Direct detection of novel expanded trinucleotide repeats in the human genome.

Authors:  M Schalling; T J Hudson; K H Buetow; D E Housman
Journal:  Nat Genet       Date:  1993-06       Impact factor: 38.330

10.  A genetic study in hypertrophic cardiomyopathies (Czech population).

Authors:  P Gregor; M Cerný
Journal:  Cor Vasa       Date:  1992
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  4 in total

Review 1.  Progress on the genetics of schizophrenia.

Authors:  A S Bassett
Journal:  J Psychiatry Neurosci       Date:  1998-11       Impact factor: 6.186

2.  An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locus.

Authors:  J B Vincent; M L Neves-Pereira; A D Paterson; E Yamamoto; S V Parikh; F Macciardi; H M Gurling; S G Potkin; C N Pato; A Macedo; M Kovacs; M Davies; J A Lieberman; H Y Meltzer; A Petronis; J L Kennedy
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

3.  Uncloned expanded CAG/CTG repeat sequences in autosomal dominant cerebellar ataxia (ADCA) detected by the repeat expansion detection (RED) method.

Authors:  M A Pujana; V Volpini; M Gratacós; J Corral; I Banchs; A Sánchez; D Genís; C Cervera; X Estivill
Journal:  J Med Genet       Date:  1998-02       Impact factor: 6.318

4.  No evidence for linkage of the CHRNA7 gene region in Canadian schizophrenia families.

Authors:  M Neves-Pereira; A S Bassett; W G Honer; D Lang; N A King; J L Kennedy
Journal:  Am J Med Genet       Date:  1998-09-07
  4 in total

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