Literature DB >> 22573628

Alanyl-tRNA synthetase mutation in a family with dominant distal hereditary motor neuropathy.

Z Zhao1, A Hashiguchi, J Hu, Y Sakiyama, Y Okamoto, S Tokunaga, L Zhu, H Shen, H Takashima.   

Abstract

OBJECTIVE: To identify a new genetic cause of distal hereditary motor neuropathy (dHMN), which is also known as a variant of Charcot-Marie-Tooth disease (CMT), in a Chinese family.
METHODS: We investigated a Chinese family with dHMN clinically, electrophysiologically, and genetically. We screened for the mutations of 28 CMT or related pathogenic genes using an originally designed microarray resequencing DNA chip.
RESULTS: Investigation of the family history revealed an autosomal dominant transmission pattern. The clinical features of the family included mild weakness and wasting of the distal muscles of the lower limb and foot deformity, without clinical sensory involvement. Electrophysiologic studies revealed motor neuropathy. MRI of the lower limbs showed accentuated fatty infiltration of the gastrocnemius and vastus lateralis muscles. All 4 affected family members had a heterozygous missense mutation c.2677G>A (p.D893N) of alanyl-tRNA synthetase (AARS), which was not found in the 4 unaffected members and control subjects.
CONCLUSION: An AARS mutation caused dHMN in a Chinese family. AARS mutations result in not only a CMT phenotype but also a dHMN phenotype.

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Year:  2012        PMID: 22573628      PMCID: PMC3359507          DOI: 10.1212/WNL.0b013e3182574f8f

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  12 in total

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2.  Alanyl-tRNA synthetase crystal structure and design for acceptor-stem recognition.

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Review 3.  Molecular genetics and mechanisms of disease in distal hereditary motor neuropathies: insights directing future genetic studies.

Authors:  A P Drew; I P Blair; G A Nicholson
Journal:  Curr Mol Med       Date:  2011-11       Impact factor: 2.222

4.  Functional analyses of glycyl-tRNA synthetase mutations suggest a key role for tRNA-charging enzymes in peripheral axons.

Authors:  Anthony Antonellis; Shih-Queen Lee-Lin; Amy Wasterlain; Paul Leo; Martha Quezado; Lev G Goldfarb; Kyungjae Myung; Shawn Burgess; Kenneth H Fischbeck; Eric D Green
Journal:  J Neurosci       Date:  2006-10-11       Impact factor: 6.167

5.  Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy.

Authors:  Albena Jordanova; Joy Irobi; Florian P Thomas; Patrick Van Dijck; Kris Meerschaert; Maarten Dewil; Ines Dierick; An Jacobs; Els De Vriendt; Velina Guergueltcheva; Chitharanjan V Rao; Ivailo Tournev; Francisco A A Gondim; Marc D'Hooghe; Veerle Van Gerwen; Patrick Callaerts; Ludo Van Den Bosch; Jean-Pièrre Timmermans; Wim Robberecht; Jan Gettemans; Johan M Thevelein; Peter De Jonghe; Ivo Kremensky; Vincent Timmerman
Journal:  Nat Genet       Date:  2006-01-22       Impact factor: 38.330

6.  Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within a single large kindred and map to a refined region on chromosome 7p15.

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7.  Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.

Authors:  Anthony Antonellis; Rachel E Ellsworth; Nyamkhishig Sambuughin; Imke Puls; Annette Abel; Shih-Queen Lee-Lin; Albena Jordanova; Ivo Kremensky; Kyproula Christodoulou; Lefkos T Middleton; Kumaraswamy Sivakumar; Victor Ionasescu; Benoit Funalot; Jeffery M Vance; Lev G Goldfarb; Kenneth H Fischbeck; Eric D Green
Journal:  Am J Hum Genet       Date:  2003-04-10       Impact factor: 11.025

8.  A major determinant for binding and aminoacylation of tRNA(Ala) in cytoplasmic Alanyl-tRNA synthetase is mutated in dominant axonal Charcot-Marie-Tooth disease.

Authors:  Philippe Latour; Christel Thauvin-Robinet; Chantal Baudelet-Méry; Pierre Soichot; Veronica Cusin; Laurence Faivre; Marie-Claire Locatelli; Martine Mayençon; Annie Sarcey; Emmanuel Broussolle; William Camu; Albert David; Robert Rousson
Journal:  Am J Hum Genet       Date:  2009-12-31       Impact factor: 11.025

9.  Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome.

Authors:  Christian Windpassinger; Michaela Auer-Grumbach; Joy Irobi; Heema Patel; Erwin Petek; Gerd Hörl; Roland Malli; Johanna A Reed; Ines Dierick; Nathalie Verpoorten; Thomas T Warner; Christos Proukakis; Peter Van den Bergh; Christine Verellen; Lionel Van Maldergem; Luciano Merlini; Peter De Jonghe; Vincent Timmerman; Andrew H Crosby; Klaus Wagner
Journal:  Nat Genet       Date:  2004-02-22       Impact factor: 38.330

10.  Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2.

Authors:  H Houlden; M Laura; F Wavrant-De Vrièze; J Blake; N Wood; M M Reilly
Journal:  Neurology       Date:  2008-10-01       Impact factor: 9.910

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  32 in total

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2.  A novel AARS mutation in a family with dominant myeloneuropathy.

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Review 4.  Predicting the pathogenicity of aminoacyl-tRNA synthetase mutations.

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Review 5.  Human aminoacyl-tRNA synthetases in diseases of the nervous system.

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Journal:  RNA Biol       Date:  2017-06-30       Impact factor: 4.652

6.  A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy.

Authors:  Pei-Chien Tsai; Bing-Wen Soong; Inès Mademan; Yen-Hua Huang; Chia-Rung Liu; Cheng-Tsung Hsiao; Hung-Ta Wu; Tze-Tze Liu; Yo-Tsen Liu; Yen-Ting Tseng; Kon-Ping Lin; Ueng-Cheng Yang; Ki Wha Chung; Byung-Ok Choi; Garth A Nicholson; Marina L Kennerson; Chih-Chiang Chan; Peter De Jonghe; Tzu-Hao Cheng; Yi-Chu Liao; Stephan Züchner; Jonathan Baets; Yi-Chung Lee
Journal:  Brain       Date:  2017-05-01       Impact factor: 13.501

7.  A novel homozygous mutation of the TFG gene in a patient with early onset spastic paraplegia and later onset sensorimotor polyneuropathy.

Authors:  Takuya Miyabayashi; Tatsuhiro Ochiai; Naoki Suzuki; Masashi Aoki; Takehiko Inui; Yukimune Okubo; Ryo Sato; Noriko Togashi; Hiroshi Takashima; Hiroyuki Ishiura; Shoji Tsuji; Kishin Koh; Yoshihisa Takiyama; Kazuhiro Haginoya
Journal:  J Hum Genet       Date:  2018-11-22       Impact factor: 3.172

8.  Clinical and mutational spectrum of Japanese patients with recessive variants in SH3TC2.

Authors:  Jun-Hui Yuan; Akihiro Hashiguchi; Yuji Okamoto; Akiko Yoshimura; Masahiro Ando; Kazutaka Shiomi; Kayoko Saito; Makoto Takahashi; Keiko Ichinose; Takuma Ohmichi; Kazushi Ichikawa; Adachi Tadashi; Hiroshi Takigawa; Hidehiro Shibayama; Hiroshi Takashima
Journal:  J Hum Genet       Date:  2018-01-10       Impact factor: 3.172

9.  Loss of function mutations in HARS cause a spectrum of inherited peripheral neuropathies.

Authors:  Dana Safka Brozkova; Tine Deconinck; Laurie Beth Griffin; Andreas Ferbert; Jana Haberlova; Radim Mazanec; Petra Lassuthova; Christian Roth; Thanita Pilunthanakul; Bernd Rautenstrauss; Andreas R Janecke; Petra Zavadakova; Roman Chrast; Carlo Rivolta; Stephan Zuchner; Anthony Antonellis; Asim A Beg; Peter De Jonghe; Jan Senderek; Pavel Seeman; Jonathan Baets
Journal:  Brain       Date:  2015-06-13       Impact factor: 13.501

Review 10.  Neurodegenerative Charcot-Marie-Tooth disease as a case study to decipher novel functions of aminoacyl-tRNA synthetases.

Authors:  Na Wei; Qian Zhang; Xiang-Lei Yang
Journal:  J Biol Chem       Date:  2019-01-14       Impact factor: 5.157

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