Literature DB >> 15876586

JP-3 gene polymorphism in a healthy population of Serbia and Montenegro.

M Keckarević1, D Savić, S Romac.   

Abstract

Expansions of CTG repeats in JP-3 gene are associated with a phenotype similar to Huntington disease. These expansions are the cause of Huntington disease like-2 (HDL-2) phenotype. CTG repeats in JP-3 gene are polymorphic in healthy population. Analyses of CTG repeat polymorphism of JP-3 gene in various healthy populations could help in estimating the population at risk for developing HDL-2. CTG repeat polymorphism of JP-3 gene was analysed in healthy population of Serbia and Montenegro. Study included 198 unrelated subjects. Analyses of JP-3 locus were performed using PCR and sequencing. Six different JP-3 alleles were obtained and they were in the range of 11 to 18 CTG repeats showing a bimodal distribution, with peaks at 14 and 16. Results show that the distribution of JP-3 alleles in population of Serbia and Montenegro is consistent with distributions in other analysed populations. The absence of alleles with more then 18 CTG repeats suggests that HDL-2 is very rare in the populations of Serbia and Montenegro.

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Year:  2005        PMID: 15876586     DOI: 10.1007/bf02715892

Source DB:  PubMed          Journal:  J Genet        ISSN: 0022-1333            Impact factor:   1.166


  7 in total

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Authors:  M Nishi; A Mizushima; K i Nakagawara; H Takeshima
Journal:  Biochem Biophys Res Commun       Date:  2000-07-14       Impact factor: 3.575

2.  Trinucleotide repeat expansions in the junctophilin-3 gene are not found in Caucasian patients with a Huntington's disease-like phenotype.

Authors:  Ingrid Bauer; Martin Gencik; Franco Laccone; Hartmut Peters; Bernhard H F Weber; Elke Holinski Feder; Helga Weirich; Deborah J Morris-Rosendahl; Arndt Rolfs; Alexandra Gencikova; Peter Bauer; Gregor K Wenning; Jörg T Epplen; Susan E Holmes; Russell L Margolis; Christopher A Ross; Olaf Riess
Journal:  Ann Neurol       Date:  2002-05       Impact factor: 10.422

3.  Fast and sensitive silver staining of DNA in polyacrylamide gels.

Authors:  B J Bassam; G Caetano-Anollés; P M Gresshoff
Journal:  Anal Biochem       Date:  1991-07       Impact factor: 3.365

4.  CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patients.

Authors:  G Stevanin; A Camuzat; S E Holmes; C Julien; R Sahloul; C Dodé; V Hahn-Barma; C A Ross; R L Margolis; A Durr; A Brice
Journal:  Neurology       Date:  2002-03-26       Impact factor: 9.910

5.  A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2.

Authors:  S E Holmes; E O'Hearn; A Rosenblatt; C Callahan; H S Hwang; R G Ingersoll-Ashworth; A Fleisher; G Stevanin; A Brice; N T Potter; C A Ross; R L Margolis
Journal:  Nat Genet       Date:  2001-12       Impact factor: 38.330

6.  Junctophilins: a novel family of junctional membrane complex proteins.

Authors:  H Takeshima; S Komazaki; M Nishi; M Iino; K Kangawa
Journal:  Mol Cell       Date:  2000-07       Impact factor: 17.970

7.  Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.

Authors:  Giovanni Stevanin; Hiroto Fujigasaki; Anne-Sophie Lebre; Agnes Camuzat; Cecile Jeannequin; Catherine Dode; Junko Takahashi; Chankranira San; Robert Bellance; Alexis Brice; Alexandra Durr
Journal:  Brain       Date:  2003-05-06       Impact factor: 13.501

  7 in total

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