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

被引:27
作者
Cagnoli, C
Stevanin, G
Michielotto, C
Promis, GG
Brussino, A
Pappi, P
Durr, A
Dragone, E
Viemont, M
Gellera, C
Brice, A
Migone, N
Brusco, A
机构
[1] Univ Turin, Dipartimento Genet Biol & Biochim, I-10126 Turin, Italy
[2] Grp Hosp Pitie Salpetriere, INSERM, U679, F-75634 Paris, France
[3] Grp Hosp Pitie Salpetriere, APHP, Dept Genet Cytogenet & Embryol, F-75634 Paris, France
[4] SCDU Genet Med, Azienda Osped San Giovanni Battista Torino, Turin, Italy
[5] Ist Nazl Neurol C Besta, Div Biochim & Genet, Milan, Italy
关键词
D O I
10.2353/jmoldx.2006.050043
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
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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收藏
页码:128 / 132
页数:5
相关论文
共 19 条
[1]   Ataxin-7 aggregation and ubiquitination in infantile SCA7 with 180 CAG repeats [J].
Ansorge, O ;
Giunti, P ;
Michalik, A ;
Van Broeckhoven, C ;
Harding, B ;
Wood, N ;
Scaravilli, F .
ANNALS OF NEUROLOGY, 2004, 56 (03) :448-452
[2]  
Babovic-Vuksanovic D, 1998, AM J MED GENET, V79, P383
[3]   Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotype [J].
Benton, CS ;
de Silva, R ;
Rutledge, SL ;
Bohlega, S ;
Ashizawa, T ;
Zoghbi, HY .
NEUROLOGY, 1998, 51 (04) :1081-1086
[4]   Detection of large pathogenic expansions in FRDA1, SCA10, and SCA12 genes using a simple fluorescent repeat-primed PCR assay [J].
Cagnoli, C ;
Michielotto, C ;
Matsuura, T ;
Ashizawa, T ;
Margolis, RL ;
Holmes, SE ;
Gellera, C ;
Migone, N ;
Brusco, A .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2004, 6 (02) :96-100
[5]   Molecular and clinical correlations in spinocerebellar ataxia 2: A study of 32 families [J].
Cancel, G ;
Durr, A ;
Didierjean, O ;
Imbert, G ;
Burk, K ;
Lezin, A ;
Belal, S ;
Benomar, A ;
AbadaBendib, M ;
Vial, C ;
Guimaraes, J ;
Chneiweiss, H ;
Stevanin, G ;
Yvert, G ;
Abbas, N ;
Saudou, F ;
Lebre, AS ;
Yahyaoui, M ;
Hentati, F ;
Vernant, JC ;
Klockgether, T ;
Mandel, JL ;
Agid, Y ;
Brice, A .
HUMAN MOLECULAR GENETICS, 1997, 6 (05) :709-715
[6]   Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7) [J].
David, G ;
Dürr, A ;
Stevanin, G ;
Cancel, G ;
Abbas, N ;
Benomar, A ;
Belal, S ;
Lebre, AS ;
Abada-Bendib, M ;
Grid, D ;
Holmberg, M ;
Yahyaoui, M ;
Hentati, F ;
Chkili, T ;
Agid, Y ;
Brice, A .
HUMAN MOLECULAR GENETICS, 1998, 7 (02) :165-170
[7]   Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion [J].
David, G ;
Abbas, N ;
Stevanin, G ;
Durr, A ;
Yvert, G ;
Cancel, G ;
Weber, C ;
Imbert, G ;
Saudou, F ;
Antoniou, E ;
Drabkin, H ;
Gemmill, R ;
Giunti, P ;
Benomar, A ;
Wood, N ;
Ruberg, M ;
Agid, Y ;
Mandel, JL ;
Brice, A .
NATURE GENETICS, 1997, 17 (01) :65-70
[8]   Myotonic dystrophy type 2 - Molecular, diagnostic and clinical spectrum [J].
Day, JW ;
Ricker, K ;
Jacobsen, JF ;
Rasmussen, LJ ;
Dick, KA ;
Kress, W ;
Schneider, C ;
Koch, MC ;
Beilman, GJ ;
Harrison, AR ;
Dalton, JC ;
Ranum, LPW .
NEUROLOGY, 2003, 60 (04) :657-664
[9]   Expanded CAG repeats in Swedish spinocerebellar ataxia type 7 (SCA7) patients: effect of CAG repeat length on the clinical manifestation [J].
Johansson, J ;
Forsgren, L ;
Sandgren, O ;
Brice, A ;
Holmgren, G ;
Holmberg, M .
HUMAN MOLECULAR GENETICS, 1998, 7 (02) :171-176
[10]   Childhood-onset ataxia: Testing for large CAG-repeats in SCA2 and SCA7 [J].
Mao, R ;
Aylsworth, AS ;
Potter, N ;
Wilson, WG ;
Breningstall, G ;
Wick, MJ ;
Babovic-Vuksanovic, D ;
Nance, M ;
Patterson, MC ;
Gomoz, CM ;
Snow, K .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 110 (04) :338-345