Literature DB >> 23129421

The SETX missense variation spectrum as evaluated in patients with ALS4-like motor neuron diseases.

Larissa Arning1, Jörg T Epplen, Elisa Rahikkala, Corinna Hendrich, Albert C Ludolph, Anne-Dorte Sperfeld.   

Abstract

Mutations in the senataxin (SETX) gene can cause amyotrophic lateral sclerosis 4 (ALS4), an autosomal dominant form of juvenile onset amyotrophic lateral sclerosis, or result in autosomal recessive ataxia with oculomotor apraxia type 2. Great caution regarding the possible disease causation, especially of missense variations, has to be taken. Here, we evaluated the significance of all previously reported SETX missense mutations as well as six newly identified variations in 54 patients suspected of having ALS4. Yet, epidemiologic and in silico evidence indicates that all newly identified variations and two previously published ALS4-related missense variations (C1554G and I2547T) are most likely non-pathogenic, demonstrating the problems of interpretation of SETX missense alleles in the absence of functional assays.

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Year:  2012        PMID: 23129421     DOI: 10.1007/s10048-012-0347-4

Source DB:  PubMed          Journal:  Neurogenetics        ISSN: 1364-6745            Impact factor:   2.660


  23 in total

Review 1.  El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis.

Authors:  B R Brooks; R G Miller; M Swash; T L Munsat
Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord       Date:  2000-12

2.  Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study.

Authors:  C Criscuolo; L Chessa; S Di Giandomenico; P Mancini; F Saccà; G S Grieco; M Piane; F Barbieri; G De Michele; S Banfi; F Pierelli; N Rizzuto; F M Santorelli; L Gallosti; A Filla; C Casali
Journal:  Neurology       Date:  2006-04-25       Impact factor: 9.910

3.  Novel mutations in the senataxin DNA/RNA helicase domain in ataxia with oculomotor apraxia 2.

Authors:  Brent L Fogel; Susan Perlman
Journal:  Neurology       Date:  2006-12-12       Impact factor: 9.910

4.  Autosomal dominant juvenile amyotrophic lateral sclerosis.

Authors:  B A Rabin; J W Griffin; B J Crain; M Scavina; P F Chance; D R Cornblath
Journal:  Brain       Date:  1999-08       Impact factor: 13.501

5.  Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.

Authors:  P F Chance; B A Rabin; S G Ryan; Y Ding; M Scavina; B Crain; J W Griffin; D R Cornblath
Journal:  Am J Hum Genet       Date:  1998-03       Impact factor: 11.025

6.  Autosomal recessive ataxia with peripheral neuropathy and elevated AFP: novel mutations in SETX.

Authors:  T Asaka; H Yokoji; J Ito; K Yamaguchi; A Matsushima
Journal:  Neurology       Date:  2006-05-23       Impact factor: 9.910

7.  A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4) localizes to a 500-kb interval on chromosome 9q34.

Authors:  I P Blair; C L Bennett; A Abel; B A Rabin; J W Griffin; K H Fischbeck; D R Cornblath; P F Chance
Journal:  Neurogenetics       Date:  2000-09       Impact factor: 2.660

8.  Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder?

Authors:  P De Jonghe; M Auer-Grumbach; J Irobi; K Wagner; B Plecko; M Kennerson; D Zhu; E De Vriendt; V Van Gerwen; G Nicholson; H-P Hartung; V Timmerman
Journal:  Brain       Date:  2002-06       Impact factor: 13.501

9.  A novel mutation in the senataxin gene identified in a Chinese patient with sporadic amyotrophic lateral sclerosis.

Authors:  Zhen-hua Zhao; Wen-Zu Chen; Zhi-ying Wu; Ning Wang; Gui-xian Zhao; Wan-jin Chen; Shen-xing Murong
Journal:  Amyotroph Lateral Scler       Date:  2009-04

10.  Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2.

Authors:  Maria-Céu Moreira; Sandra Klur; Mitsunori Watanabe; Andrea H Németh; Isabelle Le Ber; José-Carlos Moniz; Christine Tranchant; Patrick Aubourg; Meriem Tazir; Lüdger Schöls; Massimo Pandolfo; Jörg B Schulz; Jean Pouget; Patrick Calvas; Masami Shizuka-Ikeda; Mikio Shoji; Makoto Tanaka; Louise Izatt; Christopher E Shaw; Abderrahim M'Zahem; Eimear Dunne; Pascale Bomont; Traki Benhassine; Naïma Bouslam; Giovanni Stevanin; Alexis Brice; João Guimarães; Pedro Mendonça; Clara Barbot; Paula Coutinho; Jorge Sequeiros; Alexandra Dürr; Jean-Marie Warter; Michel Koenig
Journal:  Nat Genet       Date:  2004-02-08       Impact factor: 38.330

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  12 in total

1.  Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2.

Authors:  Brent L Fogel; Ellen Cho; Amanda Wahnich; Fuying Gao; Olivier J Becherel; Xizhe Wang; Francesca Fike; Leslie Chen; Chiara Criscuolo; Giuseppe De Michele; Alessandro Filla; Abigail Collins; Angelika F Hahn; Richard A Gatti; Genevieve Konopka; Susan Perlman; Martin F Lavin; Daniel H Geschwind; Giovanni Coppola
Journal:  Hum Mol Genet       Date:  2014-04-23       Impact factor: 6.150

2.  Truncating mutations in APP cause a distinct neurological phenotype.

Authors:  Steven Klein; Alexander Goldman; Hane Lee; Shahnaz Ghahremani; Viraj Bhakta; Stanley F Nelson; Julian A Martinez-Agosto
Journal:  Ann Neurol       Date:  2016-08-04       Impact factor: 10.422

Review 3.  A double-edged sword: R loops as threats to genome integrity and powerful regulators of gene expression.

Authors:  Konstantina Skourti-Stathaki; Nicholas J Proudfoot
Journal:  Genes Dev       Date:  2014-07-01       Impact factor: 11.361

4.  A novel SETX gene mutation associated with Juvenile amyotrophic lateral sclerosis.

Authors:  Limin Ma; Yingying Shi; Zhongcan Chen; Shujian Li; Jiewen Zhang
Journal:  Brain Behav       Date:  2018-07-27       Impact factor: 2.708

5.  Genotype-phenotype relationship in hereditary amyotrophic lateral sclerosis.

Authors:  Satoshi Yamashita; Yukio Ando
Journal:  Transl Neurodegener       Date:  2015-07-24       Impact factor: 8.014

6.  SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.

Authors:  Lorenzo Nanetti; Simona Cavalieri; Viviana Pensato; Alessandra Erbetta; Davide Pareyson; Marta Panzeri; Giovanna Zorzi; Carlo Antozzi; Isabella Moroni; Cinzia Gellera; Alfredo Brusco; Caterina Mariotti
Journal:  Orphanet J Rare Dis       Date:  2013-08-14       Impact factor: 4.123

7.  Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.

Authors:  Elizabeth A Worthey; Gordana Raca; Jennifer J Laffin; Brandon M Wilk; Jeremy M Harris; Kathy J Jakielski; David P Dimmock; Edythe A Strand; Lawrence D Shriberg
Journal:  J Neurodev Disord       Date:  2013-10-02       Impact factor: 4.025

8.  A SUMO-dependent interaction between Senataxin and the exosome, disrupted in the neurodegenerative disease AOA2, targets the exosome to sites of transcription-induced DNA damage.

Authors:  Patricia Richard; Shuang Feng; James L Manley
Journal:  Genes Dev       Date:  2013-10-08       Impact factor: 11.361

9.  Burden of Rare Variants in ALS and Axonal Hereditary Neuropathy Genes Influence Survival in ALS: Insights from a Next Generation Sequencing Study of an Italian ALS Cohort.

Authors:  Stefania Scarlino; Teuta Domi; Laura Pozzi; Alessandro Romano; Giovanni Battista Pipitone; Yuri Matteo Falzone; Lorena Mosca; Silvana Penco; Christian Lunetta; Valeria Sansone; Lucio Tremolizzo; Raffaella Fazio; Federica Agosta; Massimo Filippi; Paola Carrera; Nilo Riva; Angelo Quattrini
Journal:  Int J Mol Sci       Date:  2020-05-08       Impact factor: 5.923

10.  Combined deficiency of Senataxin and DNA-PKcs causes DNA damage accumulation and neurodegeneration in spinal muscular atrophy.

Authors:  Annapoorna Kannan; Kanchan Bhatia; Dana Branzei; Laxman Gangwani
Journal:  Nucleic Acids Res       Date:  2018-09-19       Impact factor: 16.971

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