Literature DB >> 16436644

Large pathogenic expansions in the SCA2 and SCA7 genes can be detected by fluorescent repeat-primed polymerase chain reaction assay.

Claudia Cagnoli1, Giovanni Stevanin, Chiara Michielotto, Giovanni Gerbino Promis, Alessandro Brussino, Patrizia Pappi, Alexandra Durr, Elisa Dragone, Michelle Viemont, Cinzia Gellera, Alexis Brice, Nicola Migone, Alfredo Brusco.   

Abstract

Large expansions in the SCA2 and SCA7 genes (>100 CAG repeats) have been associated with juvenile and infantile forms of cerebellar ataxias that cannot be detected using standard polymerase chain reaction (PCR). Here, we describe a successful application of the fluorescent short tandem repeat-primed PCR method for accurate identification of these expanded repeats. The test is robust, reliable, and inexpensive and can be used to screen large series of patients, although it cannot give a precise evaluation of the size of the expansion. This test may be of practical value in prenatal diagnoses offered to affected or pre-symptomatic at-risk parents, in which a very large expansion inherited from one of the parents can be missed in the fetus by standard PCR.

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Year:  2006        PMID: 16436644      PMCID: PMC1867568          DOI: 10.2353/jmoldx.2006.050043

Source DB:  PubMed          Journal:  J Mol Diagn        ISSN: 1525-1578            Impact factor:   5.568


  19 in total

1.  Extreme expansion detection in spinocerebellar ataxia type 2 and type 7.

Authors:  Karen Snow; Rong Mao
Journal:  Methods Mol Biol       Date:  2003

2.  Transmission distortion of the mutant alleles in spinocerebellar ataxia.

Authors:  O Riess; J T Epplen; G Amoiridis; H Przuntek; L Schöls
Journal:  Hum Genet       Date:  1997-02       Impact factor: 4.132

3.  Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian family.

Authors:  J Martin; N Van Regemorter; J Del-Favero; A Löfgren; C Van Broeckhoven
Journal:  J Neurol Sci       Date:  1999-09-15       Impact factor: 3.181

4.  Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

Authors:  K Sanpei; H Takano; S Igarashi; T Sato; M Oyake; H Sasaki; A Wakisaka; K Tashiro; Y Ishida; T Ikeuchi; R Koide; M Saito; A Sato; T Tanaka; S Hanyu; Y Takiyama; M Nishizawa; N Shimizu; Y Nomura; M Segawa; K Iwabuchi; I Eguchi; H Tanaka; H Takahashi; S Tsuji
Journal:  Nat Genet       Date:  1996-11       Impact factor: 38.330

5.  Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families.

Authors:  G Cancel; A Dürr; O Didierjean; G Imbert; K Bürk; A Lezin; S Belal; A Benomar; M Abada-Bendib; C Vial; J Guimarães; H Chneiweiss; G Stevanin; G Yvert; N Abbas; F Saudou; A S Lebre; M Yahyaoui; F Hentati; J C Vernant; T Klockgether; J L Mandel; Y Agid; A Brice
Journal:  Hum Mol Genet       Date:  1997-05       Impact factor: 6.150

6.  Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion.

Authors:  G David; N Abbas; G Stevanin; A Dürr; G Yvert; G Cancel; C Weber; G Imbert; F Saudou; E Antoniou; H Drabkin; R Gemmill; P Giunti; A Benomar; N Wood; M Ruberg; Y Agid; J L Mandel; A Brice
Journal:  Nat Genet       Date:  1997-09       Impact factor: 38.330

7.  A general method for the detection of large CAG repeat expansions by fluorescent PCR.

Authors:  J P Warner; L H Barron; D Goudie; K Kelly; D Dow; D R Fitzpatrick; D J Brock
Journal:  J Med Genet       Date:  1996-12       Impact factor: 6.318

8.  Spinocerebellar ataxia type 2 (SCA2) presenting with ophthalmoplegia and developmental delay in infancy.

Authors:  Paolo Moretti; Maria Blazo; Leonardo Garcia; Dawna Armstrong; Richard Alan Lewis; Benjamin Roa; Fernando Scaglia
Journal:  Am J Med Genet A       Date:  2004-02-01       Impact factor: 2.802

9.  Ataxin-7 aggregation and ubiquitination in infantile SCA7 with 180 CAG repeats.

Authors:  Olaf Ansorge; Paola Giunti; Andrej Michalik; Christine Van Broeckhoven; Brian Harding; Nicholas Wood; Francesco Scaravilli
Journal:  Ann Neurol       Date:  2004-09       Impact factor: 10.422

10.  Detection of large pathogenic expansions in FRDA1, SCA10, and SCA12 genes using a simple fluorescent repeat-primed PCR assay.

Authors:  Claudia Cagnoli; Chiara Michielotto; Tohru Matsuura; Tetsuo Ashizawa; Russell L Margolis; Susan E Holmes; Cinzia Gellera; Nicola Migone; Alfredo Brusco
Journal:  J Mol Diagn       Date:  2004-05       Impact factor: 5.568

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  8 in total

1.  Clinical and molecular effect on offspring of a marriage of consanguineous spinocerebellar ataxia type 7 mutation carriers: a family case report.

Authors:  Jonathan J Magaña; Yessica S Tapia-Guerrero; Luis Velázquez-Pérez; Tania Cruz-Mariño; Cesar M Cerecedo-Zapata; Rocío Gómez; Nadia M Murillo-Melo; Rigoberto González-Piña; Oscar Hernández-Hernández; Bulmaro Cisneros
Journal:  Int J Clin Exp Med       Date:  2014-12-15

2.  A comprehensive clinical and genetic study of a large Mexican population with spinocerebellar ataxia type 7.

Authors:  L Velázquez-Pérez; C M Cerecedo-Zapata; O Hernández-Hernández; E Martínez-Cruz; Y S Tapia-Guerrero; R González-Piña; J Salas-Vargas; R Rodríguez-Labrada; R Gurrola-Betancourth; N Leyva-García; B Cisneros; J J Magaña
Journal:  Neurogenetics       Date:  2014-10-16       Impact factor: 2.660

3.  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

4.  Validation of sensitivity and specificity of tetraplet-primed PCR (TP-PCR) in the molecular diagnosis of myotonic dystrophy type 2 (DM2).

Authors:  Claudio Catalli; Alessandra Morgante; Raniero Iraci; Fabrizio Rinaldi; Annalisa Botta; Giuseppe Novelli
Journal:  J Mol Diagn       Date:  2010-07-08       Impact factor: 5.568

5.  Infantile childhood onset of spinocerebellar ataxia type 2.

Authors:  Roberto Di Fabio; Filippo Santorelli; Enrico Bertini; Martina Balestri; Laura Cursi; Alessandra Tessa; Francesco Pierelli; Carlo Casali
Journal:  Cerebellum       Date:  2012-06       Impact factor: 3.847

6.  Spinocerebellar ataxias in Venezuela: genetic epidemiology and their most likely ethnic descent.

Authors:  Irene Paradisi; Vassiliki Ikonomu; Sergio Arias
Journal:  J Hum Genet       Date:  2015-11-05       Impact factor: 3.172

Review 7.  An update on the neurological short tandem repeat expansion disorders and the emergence of long-read sequencing diagnostics.

Authors:  Sanjog R Chintalaphani; Sandy S Pineda; Ira W Deveson; Kishore R Kumar
Journal:  Acta Neuropathol Commun       Date:  2021-05-25       Impact factor: 7.801

8.  Genetic Distribution of Five Spinocerebellar Ataxia Microsatellite Loci in Mexican Native American Populations and Its Impact on Contemporary Mestizo Populations.

Authors:  Rocío Gómez; Yessica S Tapia-Guerrero; Bulmaro Cisneros; Lorena Orozco; César Cerecedo-Zapata; Elvia Mendoza-Caamal; Gerardo Leyva-Gómez; Norberto Leyva-García; Luis Velázquez-Pérez; Jonathan J Magaña
Journal:  Genes (Basel)       Date:  2022-01-16       Impact factor: 4.096

  8 in total

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