Literature DB >> 17098887

Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia.

Christel Depienne, Estelle Fedirko, Sylvie Forlani, Cécile Cazeneuve, Pascale Ribaï, Imed Feki, Chantal Tallaksen, Karine Nguyen, Bruno Stankoff, Merle Ruberg, Giovanni Stevanin, Alexandra Durr, Alexis Brice.   

Abstract

BACKGROUND: Point mutations in SPG4, the gene encoding spastin, are a frequent cause of autosomal dominant hereditary spastic paraplegia (AD-HSP). However, standard methods for genetic analyses fail to detect exonic microdeletions.
METHODS: 121 mutation-negative probands were screened for rearrangements in SPG4 by multiplex ligation-dependent probe amplification.
RESULTS: 24 patients with 16 different heterozygotic exon deletions in SPG4 (20%) were identified, ranging from one exon to the whole coding sequence. Comparison with 78 patients with point mutations showed a similar clinical picture but an earlier age at onset.
CONCLUSIONS: Exon deletions in SPG4 are as frequent as point mutations, and SPG4 is responsible for 40% of AD-HSP.

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Year:  2006        PMID: 17098887      PMCID: PMC2598038          DOI: 10.1136/jmg.2006.046425

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  11 in total

1.  Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia.

Authors:  Inge A Meijer; Collette K Hand; P Cossette; Denise A Figlewicz; Guy A Rouleau
Journal:  Arch Neurol       Date:  2002-02

2.  Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia.

Authors:  J Hazan; N Fonknechten; D Mavel; C Paternotte; D Samson; F Artiguenave; C S Davoine; C Cruaud; A Dürr; P Wincker; P Brottier; L Cattolico; V Barbe; J M Burgunder; J F Prud'homme; A Brice; B Fontaine; B Heilig; J Weissenbach
Journal:  Nat Genet       Date:  1999-11       Impact factor: 38.330

3.  Clinical features of hereditary spastic paraplegia due to spastin mutation.

Authors:  C J McDermott; C E Burness; J Kirby; L E Cox; D G Rao; C Hewamadduma; B Sharrack; M Hadjivassiliou; P F Chinnery; A Dalton; P J Shaw
Journal:  Neurology       Date:  2006-07-11       Impact factor: 9.910

4.  A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members.

Authors:  S H Mead; C Proukakis; N Wood; A H Crosby; G T Plant; T T Warner
Journal:  J Neurol Neurosurg Psychiatry       Date:  2001-12       Impact factor: 10.154

5.  Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.

Authors:  J E Nielsen; B Johnsen; P Koefoed; K H Scheuer; M Grønbech-Jensen; I Law; K Krabbe; A Nørremølle; H Eiberg; H Søndergård; M Dam; J F Rehfeld; C Krarup; O B Paulson; L Hasholt; S A Sørensen
Journal:  Eur J Neurol       Date:  2004-12       Impact factor: 6.089

6.  Large deletion involving the 5'-UTR in the spastin gene caused mild phenotype of autosomal dominant hereditary spastic paraplegia.

Authors:  Hiroshi Iwanaga; Akira Tsujino; Susumu Shirabe; Hiroto Eguchi; Naomi Fukushima; Norio Niikawa; Koh-Ichiro Yoshiura; Katsumi Eguchi
Journal:  Am J Med Genet A       Date:  2005-02-15       Impact factor: 2.802

7.  Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.

Authors:  N Fonknechten; D Mavel; P Byrne; C S Davoine; C Cruaud; D Bönsch; D Boentsch; D Samson; P Coutinho; M Hutchinson; P McMonagle; J M Burgunder; A Tartaglione; O Heinzlef; I Feki; T Deufel; N Parfrey; A Brice; B Fontaine; J F Prud'homme; J Weissenbach; A Dürr; J Hazan
Journal:  Hum Mol Genet       Date:  2000-03-01       Impact factor: 6.150

8.  Hereditary spastic paraplegia caused by mutations in the SPG4 gene.

Authors:  J Bürger; N Fonknechten; M Hoeltzenbein; L Neumann; E Bratanoff; J Hazan; A Reis
Journal:  Eur J Hum Genet       Date:  2000-10       Impact factor: 4.246

9.  Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia.

Authors:  S Sauter; B Miterski; S Klimpe; D Bönsch; L Schöls; A Visbeck; T Papke; H C Hopf; W Engel; T Deufel; J T Epplen; J Neesen
Journal:  Hum Mutat       Date:  2002-08       Impact factor: 4.878

10.  Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia.

Authors:  Beisha Tang; Guohua Zhao; Kun Xia; Qian Pan; Wei Luo; Lu Shen; Zhigao Long; Heping Dai; Xiaohong Zi; Hong Jiang
Journal:  Arch Neurol       Date:  2004-01
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  40 in total

Review 1.  Recent advances in the genetics of spastic paraplegias.

Authors:  Giovanni Stevanin; Merle Ruberg; Alexis Brice
Journal:  Curr Neurol Neurosci Rep       Date:  2008-05       Impact factor: 5.081

2.  The Alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV alleles.

Authors:  Philip M Boone; Bo Yuan; Ian M Campbell; Jennifer C Scull; Marjorie A Withers; Brett C Baggett; Christine R Beck; Christine J Shaw; Pawel Stankiewicz; Paolo Moretti; Wendy E Goodwin; Nichole Hein; John K Fink; Moon-Woo Seong; Soo Hyun Seo; Sung Sup Park; Izabela D Karbassi; Sat Dev Batish; Andrés Ordóñez-Ugalde; Beatriz Quintáns; María-Jesús Sobrido; Susanne Stemmler; James R Lupski
Journal:  Am J Hum Genet       Date:  2014-07-24       Impact factor: 11.025

3.  Crystal structure of the human spastin AAA domain.

Authors:  Jennifer L Taylor; Susan Roehl White; Brett Lauring; F Jon Kull
Journal:  J Struct Biol       Date:  2012-03-14       Impact factor: 2.867

4.  Screening for the hereditary spastic paraplaegias SPG4 and SPG3A with the multiplex ligation-dependent probe amplification technique in a large population of affected individuals.

Authors:  Anna Sulek; Ewelina Elert; Marta Rajkiewicz; Elzbieta Zdzienicka; Iwona Stepniak; Wioletta Krysa; Jacek Zaremba
Journal:  Neurol Sci       Date:  2011-12-28       Impact factor: 3.307

5.  Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegia.

Authors:  Rebecca Schüle; Elisabeth Brandt; Kathrin N Karle; Maria Tsaousidou; Stephan Klebe; Sven Klimpe; Michaela Auer-Grumbach; Andrew H Crosby; Christian A Hübner; Ludger Schöls; Thomas Deufel; Christian Beetz
Journal:  Neurogenetics       Date:  2008-10-15       Impact factor: 2.660

6.  Unique spectrum of SPAST variants in Estonian HSP patients: presence of benign missense changes but lack of exonic rearrangements.

Authors:  Mark Braschinsky; Riin Tamm; Christian Beetz; Elena Sachez-Ferrero; Elve Raukas; Siiri-Merike Lüüs; Katrin Gross-Paju; Catherine Boillot; Federico Canzian; Andres Metspalu; Sulev Haldre
Journal:  BMC Neurol       Date:  2010-03-09       Impact factor: 2.474

7.  A genome-scale DNA repair RNAi screen identifies SPG48 as a novel gene associated with hereditary spastic paraplegia.

Authors:  Mikołaj Słabicki; Mirko Theis; Dragomir B Krastev; Sergey Samsonov; Emeline Mundwiller; Magno Junqueira; Maciej Paszkowski-Rogacz; Joan Teyra; Anne-Kristin Heninger; Ina Poser; Fabienne Prieur; Jérémy Truchetto; Christian Confavreux; Cécilia Marelli; Alexandra Durr; Jean Philippe Camdessanche; Alexis Brice; Andrej Shevchenko; M Teresa Pisabarro; Giovanni Stevanin; Frank Buchholz
Journal:  PLoS Biol       Date:  2010-06-29       Impact factor: 8.029

8.  Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridization.

Authors:  Peter Bauer; Beate Winner; Rebecca Schüle; Claudia Bauer; Veronika Häfele; Ute Hehr; Michael Bonin; Michael Walter; Kathrin Karle; Thomas M Ringer; Olaf Riess; Jürgen Winkler; Ludger Schöls
Journal:  Neurogenetics       Date:  2008-09-12       Impact factor: 2.660

9.  The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signalling.

Authors:  Hilda T H Tsang; Thomas L Edwards; Xinnan Wang; James W Connell; Rachel J Davies; Hannah J Durrington; Cahir J O'Kane; J Paul Luzio; Evan Reid
Journal:  Hum Mol Genet       Date:  2009-07-20       Impact factor: 6.150

10.  Spastin couples microtubule severing to membrane traffic in completion of cytokinesis and secretion.

Authors:  James W Connell; Catherine Lindon; J Paul Luzio; Evan Reid
Journal:  Traffic       Date:  2008-10-29       Impact factor: 6.215

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