Literature DB >> 19697368

RNA processing defects associated with diseases of the motor neuron.

Stephen J Kolb1, Scott Sutton, Daniel R Schoenberg.   

Abstract

Rapid progress in the discovery of motor neuron disease genes in amyotrophic lateral sclerosis, the spinal muscular atrophies, hereditary motor neuropathies, and lethal congenital contracture syndromes is providing new perspectives and insights into the molecular pathogenesis of the motor neuron. Motor neuron disease genes are often expressed throughout the body with essential functions in all cells. A survey of these functions indicates that motor neurons are uniquely sensitive to perturbations in RNA processing pathways dependent on the interaction of specific RNAs with specific RNA-binding proteins, which presumably result in aberrant formation and function of ribonucleoprotein complexes. This review provides a summary of currently recognized RNA processing defects linked to human motor neuron diseases.

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Year:  2010        PMID: 19697368      PMCID: PMC3654835          DOI: 10.1002/mus.21428

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  154 in total

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2.  Unravelling mRNA export.

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3.  Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration.

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4.  Localization of the DCTN1 gene encoding p150Glued to human chromosome 2p13 by fluorescence in situ hybridization.

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Journal:  Genomics       Date:  1996-02-01       Impact factor: 5.736

Review 5.  Splicing regulation in neurologic disease.

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8.  Activation of the DExD/H-box protein Dbp5 by the nuclear-pore protein Gle1 and its coactivator InsP6 is required for mRNA export.

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9.  The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V.

Authors:  O Dubourg; H Azzedine; R Ben Yaou; J Pouget; A Barois; V Meininger; D Bouteiller; M Ruberg; A Brice; E LeGuern
Journal:  Neurology       Date:  2006-06-13       Impact factor: 9.910

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  15 in total

Review 1.  Spliceosomal small nuclear ribonucleoprotein biogenesis defects and motor neuron selectivity in spinal muscular atrophy.

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Review 4.  Common pathways of autoimmune inflammatory myopathies and genetic neuromuscular disorders.

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Review 6.  Spinal muscular atrophy and the antiapoptotic role of survival of motor neuron (SMN) protein.

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7.  Identification of cytoplasmic capping targets reveals a role for cap homeostasis in translation and mRNA stability.

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8.  Candidate proteins, metabolites and transcripts in the Biomarkers for Spinal Muscular Atrophy (BforSMA) clinical study.

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10.  EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvement.

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