Literature DB >> 20832291

The BMP signaling pathway at the Drosophila neuromuscular junction and its links to neurodegenerative diseases.

Vafa Bayat1, Manish Jaiswal, Hugo J Bellen.   

Abstract

The Drosophila neuromuscular junction (NMJ) has recently provided new insights into the roles of various proteins in neurodegenerative diseases including Amyotrophic Lateral Sclerosis (ALS), Spinal Muscular Atrophy (SMA), Multiple Sclerosis (MS) Hereditary Spastic Paraplegia (HSP), and Huntington's Disease (HD). Several developmental signaling pathways including WNT, MAPK and BMP/TGF-β signaling play important roles in the formation and growth of the Drosophila NMJ. Studies of the fly homologues of genes that cause neurodegenerative disease at the NMJ have resulted in a better understanding of the roles of these proteins in vivo. These studies may shed light on the pathological mechanisms of these diseases, with implications for reduced BMP/TGF-β signaling in ALS, SMA and HD and increased signaling in HSP and MS.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20832291      PMCID: PMC3095363          DOI: 10.1016/j.conb.2010.08.014

Source DB:  PubMed          Journal:  Curr Opin Neurobiol        ISSN: 0959-4388            Impact factor:   6.627


  52 in total

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Review 9.  Transgenesis upgrades for Drosophila melanogaster.

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2.  Spartin regulates synaptic growth and neuronal survival by inhibiting BMP-mediated microtubule stabilization.

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Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2015-06-10       Impact factor: 3.568

5.  Augmented noncanonical BMP type II receptor signaling mediates the synaptic abnormality of fragile X syndrome.

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6.  MAN1 Restricts BMP Signaling During Synaptic Growth in Drosophila.

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7.  Spg20-/- mice reveal multimodal functions for Troyer syndrome protein spartin in lipid droplet maintenance, cytokinesis and BMP signaling.

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Review 8.  Regulation of BMP activity and range in Drosophila wing development.

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10.  Hereditary spastic paraplegia-causing mutations in atlastin-1 interfere with BMPRII trafficking.

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Journal:  Mol Cell Neurosci       Date:  2012-10-16       Impact factor: 4.314

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