Literature DB >> 16928353

Genetics of motor neuron disease.

Ludo Van Den Bosch1, Vincent Timmerman.   

Abstract

The number of genes associated with motor neuron degeneration has increased considerably over the past few years. As more gene mutations are identified, the hope arises that certain common themes and/or pathways become clear. In this overview, we focus on recent discoveries related to amyotrophic lateral sclerosis (ALS), spinal muscular atrophies (SMA), and distal hereditary motor neuropathies (dHMN). It is striking that many of the mutated genes that were linked to these diseases encode proteins that are either directly or indirectly involved in axonal transport or play a role in RNA metabolism. We hypothesize that both phenomena are not only crucial for the normal functioning of motor neurons, but that they could also be interconnected. In analogy with the situation after acute stress, axonal mRNA translation followed by retrograde transport of the signal back to the nucleus could play an important role in chronic motor neuron diseases. We hope that information on the genetic causes of these diseases and the insight into the pathologic processes involved could ultimately lead to therapeutic strategies that prevent or at least slow this degenerative process.

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Year:  2006        PMID: 16928353     DOI: 10.1007/s11910-996-0024-9

Source DB:  PubMed          Journal:  Curr Neurol Neurosci Rep        ISSN: 1528-4042            Impact factor:   5.081


  57 in total

1.  From snails to sciatic nerve: Retrograde injury signaling from axon to soma in lesioned neurons.

Authors:  Eran Perlson; Shlomit Hanz; Katalin F Medzihradszky; Alma L Burlingame; Mike Fainzilber
Journal:  J Neurobiol       Date:  2004-02-05

2.  Lentiviral-mediated silencing of SOD1 through RNA interference retards disease onset and progression in a mouse model of ALS.

Authors:  Cédric Raoul; Toufik Abbas-Terki; Jean-Charles Bensadoun; Sandrine Guillot; Georg Haase; Jolanta Szulc; Christopher E Henderson; Patrick Aebischer
Journal:  Nat Med       Date:  2005-03-13       Impact factor: 53.440

3.  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

4.  Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1.

Authors:  K Grohmann; M Schuelke; A Diers; K Hoffmann; B Lucke; C Adams; E Bertini; H Leonhardt-Horti; F Muntoni; R Ouvrier; A Pfeufer; R Rossi; L Van Maldergem; J M Wilmshurst; T F Wienker; M Sendtner; S Rudnik-Schöneborn; K Zerres; C Hübner
Journal:  Nat Genet       Date:  2001-09       Impact factor: 38.330

5.  The first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological function.

Authors:  Chris Panzeri; Clara De Palma; Andrea Martinuzzi; Andrea Daga; Gianni De Polo; Nereo Bresolin; Christopher C Miller; Elizabeth L Tudor; Emilio Clementi; Maria T Bassi
Journal:  Brain       Date:  2006-05-02       Impact factor: 13.501

Review 6.  Is spinal muscular atrophy the result of defects in motor neuron processes?

Authors:  Michael Briese; Behrooz Esmaeili; David B Sattelle
Journal:  Bioessays       Date:  2005-09       Impact factor: 4.345

Review 7.  Defective neurofilament transport in mouse models of amyotrophic lateral sclerosis: a review.

Authors:  Mala V Rao; Ralph A Nixon
Journal:  Neurochem Res       Date:  2003-07       Impact factor: 3.996

8.  The phenotype of motor neuropathies associated with BSCL2 mutations is broader than Silver syndrome and distal HMN type V.

Authors:  Joy Irobi; Peter Van den Bergh; Luciano Merlini; Christine Verellen; Lionel Van Maldergem; Ines Dierick; Nathalie Verpoorten; Albena Jordanova; Christian Windpassinger; Els De Vriendt; Veerle Van Gerwen; Michaela Auer-Grumbach; Klaus Wagner; Vincent Timmerman; Peter De Jonghe
Journal:  Brain       Date:  2004-07-08       Impact factor: 13.501

9.  Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy.

Authors:  Oleg V Evgrafov; Irena Mersiyanova; Joy Irobi; Ludo Van Den Bosch; Ines Dierick; Conrad L Leung; Olga Schagina; Nathalie Verpoorten; Katrien Van Impe; Valeriy Fedotov; Elena Dadali; Michaela Auer-Grumbach; Christian Windpassinger; Klaus Wagner; Zoran Mitrovic; David Hilton-Jones; Kevin Talbot; Jean-Jacques Martin; Natalia Vasserman; Svetlana Tverskaya; Alexander Polyakov; Ronald K H Liem; Jan Gettemans; Wim Robberecht; Peter De Jonghe; Vincent Timmerman
Journal:  Nat Genet       Date:  2004-05-02       Impact factor: 38.330

10.  Axonal defects in mouse models of motoneuron disease.

Authors:  Sibylle Jablonka; Stefan Wiese; Michael Sendtner
Journal:  J Neurobiol       Date:  2004-02-05
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  8 in total

1.  Autosomal dominant late-onset spinal motor neuronopathy is linked to a new locus on chromosome 22q11.2-q13.2.

Authors:  Sini Penttilä; Manu Jokela; Peter Hackman; Anna Maija Saukkonen; Jari Toivanen; Bjarne Udd
Journal:  Eur J Hum Genet       Date:  2012-04-25       Impact factor: 4.246

2.  Maintaining muscle mitochondria via transsynaptic signaling.

Authors:  Jennifer B Long; David Van Vactor
Journal:  Dev Cell       Date:  2012-02-14       Impact factor: 12.270

Review 3.  Current Perspective of Stem Cell Therapy in Neurodegenerative and Metabolic Diseases.

Authors:  Ajay Kumar; Karthikeyan Narayanan; Ravi Kumar Chaudhary; Sachin Mishra; Sundramurthy Kumar; Kumar Jayaseelan Vinoth; Parasuraman Padmanabhan; Balázs Gulyás
Journal:  Mol Neurobiol       Date:  2016-11-04       Impact factor: 5.590

Review 4.  Genetic rodent models of amyotrophic lateral sclerosis.

Authors:  L Van Den Bosch
Journal:  J Biomed Biotechnol       Date:  2011-01-02

5.  Mutant glycyl-tRNA synthetase (Gars) ameliorates SOD1(G93A) motor neuron degeneration phenotype but has little affect on Loa dynein heavy chain mutant mice.

Authors:  Gareth T Banks; Virginie Bros-Facer; Hazel P Williams; Ruth Chia; Francesca Achilli; J Barney Bryson; Linda Greensmith; Elizabeth M C Fisher
Journal:  PLoS One       Date:  2009-07-13       Impact factor: 3.240

6.  The nuclear factor kappaB-activator gene PLEKHG5 is mutated in a form of autosomal recessive lower motor neuron disease with childhood onset.

Authors:  Isabelle Maystadt; René Rezsöhazy; Martine Barkats; Sandra Duque; Pascal Vannuffel; Sophie Remacle; Barbara Lambert; Mustapha Najimi; Etienne Sokal; Arnold Munnich; Louis Viollet; Christine Verellen-Dumoulin
Journal:  Am J Hum Genet       Date:  2007-05-16       Impact factor: 11.025

7.  A novel locus for distal motor neuron degeneration maps to chromosome 7q34-q36.

Authors:  Sumana Gopinath; Ian P Blair; Marina L Kennerson; Jennifer C Durnall; Garth A Nicholson
Journal:  Hum Genet       Date:  2007-03-13       Impact factor: 5.881

8.  Genetic heterogeneity of motor neuropathies.

Authors:  Boglarka Bansagi; Helen Griffin; Roger G Whittaker; Thalia Antoniadi; Teresinha Evangelista; James Miller; Mark Greenslade; Natalie Forester; Jennifer Duff; Anna Bradshaw; Stephanie Kleinle; Veronika Boczonadi; Hannah Steele; Venkateswaran Ramesh; Edit Franko; Angela Pyle; Hanns Lochmüller; Patrick F Chinnery; Rita Horvath
Journal:  Neurology       Date:  2017-03-01       Impact factor: 9.910

  8 in total

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