Reduced levels of survival motor neuron protein leads to aberrant motoneuron growth in a Xenopus model of muscular atrophy

Neurogenetics. 2010 Feb;11(1):27-40. doi: 10.1007/s10048-009-0200-6. Epub 2009 Jun 11.

Abstract

Spinal muscular atrophy (SMA) is a neurodegenerative disease characterized by motor neuron loss and skeletal muscle atrophy. The loss of function of the smn1 gene, the main supplier of survival motor neuron protein (SMN) protein in human, leads to reduced levels of SMN and eventually to SMA. Here, we ask if the amphibian Xenopus tropicalis can be a good model system to study SMA. Inhibition of the production of SMN using antisense morpholinos leads to caudal muscular atrophy in tadpoles. Of note, early developmental patterning of muscles and motor neurons is unaffected in this system as well as acetylcholine receptors clustering. Muscular atrophy seems to rather result from aberrant pathfinding and growth arrest and/or shortening of motor axons. This event occurs in the absence of neuronal cell bodies apoptosis, a process comparable to that of amyotrophic lateral sclerosis. Xenopus tropicalis is revealed as a complementary animal model for the study of SMA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Apoptosis
  • Base Sequence
  • Disease Models, Animal
  • Gene Expression Regulation, Developmental*
  • Humans
  • In Situ Hybridization
  • Molecular Sequence Data
  • Muscular Atrophy, Spinal / genetics*
  • Oligonucleotides, Antisense / pharmacology
  • Receptors, Cholinergic / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Homology, Amino Acid
  • Survival of Motor Neuron 1 Protein / biosynthesis*
  • Xenopus

Substances

  • Oligonucleotides, Antisense
  • Receptors, Cholinergic
  • Survival of Motor Neuron 1 Protein