Literature DB >> 23834483

Identification of FUS p.R377W in essential tremor.

A Rajput1, A H Rajput, M L Rajput, M Encarnacion, C Q Bernales, J P Ross, M J Farrer, C Vilariño-Güell.   

Abstract

BACKGROUND AND
PURPOSE: Exome sequencing analysis has recently identified a nonsense mutation in fused in sarcoma (FUS) segregating with essential tremor (ET) within a large French-Canadian family. Further characterization of FUS resulted in the identification of additional mutations in ET patients; however, their pathogenicity still remains to be confirmed. The role of FUS in an independent cohort of ET patients from Canada was evaluated.
METHODS: The entire coding sequence of FUS in 217 patients diagnosed with ET was analyzed and two missense variants in 219 healthy controls were genotyped by Sanger sequencing.
RESULTS: Sequencing of FUS identified a previously reported non-pathogenic mutation p.G174_G175del in one ET patient and two healthy controls, and a novel p.R377W in one patient with family history of disease. This mutation is highly conserved and strongly predicted to be damaging by in silico analysis.
CONCLUSION: This study has identified a novel FUS p.R377W substitution in ET patients. Additional genotyping studies in a large number of ET patients and controls are necessary to conclusively define its pathogenicity.
© 2013 The Author(s) European Journal of Neurology © 2013 EFNS.

Entities:  

Keywords:  FUS; amyotrophic lateral sclerosis; essential tremor; mutation

Mesh:

Substances:

Year:  2013        PMID: 23834483      PMCID: PMC5092174          DOI: 10.1111/ene.12231

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  10 in total

1.  Pathogenicity of exonic indels in fused in sarcoma in amyotrophic lateral sclerosis.

Authors:  Nicola J Rutherford; Nicole A Finch; Mariely DeJesus-Hernandez; Richard J P Crook; Catherine Lomen-Hoerth; Zbigniew K Wszolek; Ryan J Uitti; Neill R Graff-Radford; Rosa Rademakers
Journal:  Neurobiol Aging       Date:  2010-11-12       Impact factor: 4.673

Review 2.  Essential tremor: emerging views of a common disorder.

Authors:  Julián Benito-León; Elan D Louis
Journal:  Nat Clin Pract Neurol       Date:  2006-12

3.  Mutations of FUS gene in sporadic amyotrophic lateral sclerosis.

Authors:  Lucia Corrado; Roberto Del Bo; Barbara Castellotti; Antonia Ratti; Cristina Cereda; Silvana Penco; Gianni Sorarù; Yari Carlomagno; Serena Ghezzi; Viviana Pensato; Claudia Colombrita; Stella Gagliardi; Lorena Cozzi; Valeria Orsetti; Michelangelo Mancuso; Gabriele Siciliano; Letizia Mazzini; Giacomo Pietro Comi; Cinzia Gellera; Mauro Ceroni; Sandra D'Alfonso; Vincenzo Silani
Journal:  J Med Genet       Date:  2009-10-26       Impact factor: 6.318

4.  Diagnostic criteria for essential tremor: a population perspective.

Authors:  E D Louis; B Ford; H Lee; H Andrews; G Cameron
Journal:  Arch Neurol       Date:  1998-06

5.  Genetic analysis of the fused in sarcoma gene in Chinese Han patients with essential tremor.

Authors:  Wen Zheng; Xiong Deng; Hui Liang; Zhi Song; Kai Gao; Yan Yang; Hao Deng
Journal:  Neurobiol Aging       Date:  2013-04-09       Impact factor: 4.673

6.  Investigating the role of FUS exonic variants in essential tremor.

Authors:  Catherine Labbé; Alexandra I Soto-Ortolaza; Sruti Rayaprolu; Andrea M Harriott; Audrey J Strongosky; Ryan J Uitti; Jay A Van Gerpen; Zbigniew K Wszolek; Owen A Ross
Journal:  Parkinsonism Relat Disord       Date:  2013-04-16       Impact factor: 4.891

7.  Characterization of DCTN1 genetic variability in neurodegeneration.

Authors:  C Vilariño-Güell; C Wider; A I Soto-Ortolaza; S A Cobb; J M Kachergus; B H Keeling; J C Dachsel; M M Hulihan; D W Dickson; Z K Wszolek; R J Uitti; N R Graff-Radford; B F Boeve; K A Josephs; B Miller; K B Boylan; K Gwinn; C H Adler; J O Aasly; F Hentati; A Destée; A Krygowska-Wajs; M-C Chartier-Harlin; O A Ross; R Rademakers; M J Farrer
Journal:  Neurology       Date:  2009-06-09       Impact factor: 9.910

8.  Exome sequencing identifies FUS mutations as a cause of essential tremor.

Authors:  Nancy D Merner; Simon L Girard; Hélène Catoire; Cynthia V Bourassa; Véronique V Belzil; Jean-Baptiste Rivière; Pascale Hince; Annie Levert; Alexandre Dionne-Laporte; Dan Spiegelman; Anne Noreau; Sabrina Diab; Anna Szuto; Hélène Fournier; John Raelson; Majid Belouchi; Michel Panisset; Patrick Cossette; Nicolas Dupré; Geneviève Bernard; Sylvain Chouinard; Patrick A Dion; Guy A Rouleau
Journal:  Am J Hum Genet       Date:  2012-08-02       Impact factor: 11.025

9.  FUS in familial essential tremor - the search for common causes is still on.

Authors:  Peter Hedera; Thomas L Davis; Fenna T Phibbs; P David Charles; Mark S LeDoux
Journal:  Parkinsonism Relat Disord       Date:  2013-05-06       Impact factor: 4.891

10.  Genetic analysis of the FUS/TLS gene in essential tremor.

Authors:  N Parmalee; K Mirzozoda; S Kisselev; N Merner; P Dion; G Rouleau; L Clark; E D Louis
Journal:  Eur J Neurol       Date:  2012-11-01       Impact factor: 6.089

  10 in total
  11 in total

1.  Movement disorders: novel FUS gene variants linked to essential tremor.

Authors:  Heather Wood
Journal:  Nat Rev Neurol       Date:  2013-07-23       Impact factor: 42.937

Review 2.  Challenges in essential tremor genetics.

Authors:  L N Clark; E D Louis
Journal:  Rev Neurol (Paris)       Date:  2015-05-21       Impact factor: 2.607

3.  Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor.

Authors:  Hyun Hor; Ludmila Francescatto; Luca Bartesaghi; Sara Ortega-Cubero; Maria Kousi; Oswaldo Lorenzo-Betancor; Felix J Jiménez-Jiménez; Alexandre Gironell; Jordi Clarimón; Oliver Drechsel; José A G Agúndez; Daniela Kenzelmann Broz; Ruth Chiquet-Ehrismann; Alberto Lleó; Francisco Coria; Elena García-Martin; Hortensia Alonso-Navarro; Maria J Martí; Jaume Kulisevsky; Charlotte N Hor; Stephan Ossowski; Roman Chrast; Nicholas Katsanis; Pau Pastor; Xavier Estivill
Journal:  Hum Mol Genet       Date:  2015-07-17       Impact factor: 6.150

Review 4.  The role of FUS gene variants in neurodegenerative diseases.

Authors:  Hao Deng; Kai Gao; Joseph Jankovic
Journal:  Nat Rev Neurol       Date:  2014-05-20       Impact factor: 42.937

Review 5.  Essential tremor.

Authors:  Lorraine N Clark; Elan D Louis
Journal:  Handb Clin Neurol       Date:  2018

6.  Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease.

Authors:  Hilal Unal Gulsuner; Suleyman Gulsuner; Fatma Nazli Mercan; Onur Emre Onat; Tom Walsh; Hashem Shahin; Ming K Lee; Okan Dogu; Tulay Kansu; Haluk Topaloglu; Bulent Elibol; Cenk Akbostanci; Mary-Claire King; Tayfun Ozcelik; Ayse B Tekinay
Journal:  Proc Natl Acad Sci U S A       Date:  2014-11-24       Impact factor: 11.205

7.  Identification of candidate genes for familial early-onset essential tremor.

Authors:  Xinmin Liu; Nora Hernandez; Sergey Kisselev; Aris Floratos; Ashley Sawle; Iuliana Ionita-Laza; Ruth Ottman; Elan D Louis; Lorraine N Clark
Journal:  Eur J Hum Genet       Date:  2015-10-28       Impact factor: 4.246

8.  A loss of FUS/TLS function leads to impaired cellular proliferation.

Authors:  C L Ward; K J Boggio; B N Johnson; J B Boyd; S Douthwright; S A Shaffer; J E Landers; M A Glicksman; D A Bosco
Journal:  Cell Death Dis       Date:  2014-12-11       Impact factor: 8.469

Review 9.  Role of FET proteins in neurodegenerative disorders.

Authors:  Francesca Svetoni; Paola Frisone; Maria Paola Paronetto
Journal:  RNA Biol       Date:  2016-07-14       Impact factor: 4.652

Review 10.  Genomic Markers for Essential Tremor.

Authors:  Félix Javier Jiménez-Jiménez; Hortensia Alonso-Navarro; Elena García-Martín; Ignacio Álvarez; Pau Pastor; José A G Agúndez
Journal:  Pharmaceuticals (Basel)       Date:  2021-05-27
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.