• Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy.

Proximal spinal muscular atrophy (SMA) is a common motor neuron disease in humans and in its most severe form causes death by the age of 2 years. It is caused by defects in the telomeric survival motor neuron gene ( SMN1 ), but patients retain at least one copy of a highly homologous gene, centromeric SMN ( SMN2 ). Mice possess only one survival motor neuron gene ( Smn ) whose loss is embryonic lethal. Therefore, to obtain a mouse model of SMA we created transgenic mice that express human SMN2 and mated these onto the null Smn (-/-)background. We show that Smn (-/-); SMN2 mice carrying one or two copies of the transgene have normal numbers of motor neurons at birth, but vastly reduced numbers by postnatal day 5, and subsequently die. This closely resembles a severe type I SMA phenotype in humans and is the first report of an animal model of the disease. Eight copies of the transgene rescues this phenotype in the mice indicating that phenotypic severity can be modulated by SMN2 copy number. These results show that SMA is caused by insufficient SMN production by the SMN2 gene and that increased expression of the SMN2 gene may provide a strategy for treating SMA patients.

Pubmed ID: 10655541

Authors

  • Monani UR
  • Sendtner M
  • Coovert DD
  • Parsons DW
  • Andreassi C
  • Le TT
  • Jablonka S
  • Schrank B
  • Rossoll W
  • Rossol W
  • Prior TW
  • Morris GE
  • Burghes AH

Journal

Human molecular genetics

Publication Data

February 12, 2000

Associated Grants

  • Agency: NINDS NIH HHS, Id: NS38650
  • Agency: NINDS NIH HHS, Id: R01 NS038650

Mesh Terms

  • Animals
  • Animals, Newborn
  • Blotting, Northern
  • Blotting, Western
  • Brain Stem
  • Centromere
  • Cyclic AMP Response Element-Binding Protein
  • Disease Models, Animal
  • Exons
  • Gene Dosage
  • Genotype
  • Humans
  • In Vitro Techniques
  • Mice
  • Mice, Transgenic
  • Microinjections
  • Motor Neurons
  • Muscular Atrophy, Spinal
  • Nerve Tissue Proteins
  • RNA-Binding Proteins
  • Reverse Transcriptase Polymerase Chain Reaction
  • SMN Complex Proteins
  • Spinal Cord
  • Survival of Motor Neuron 1 Protein
  • Survival of Motor Neuron 2 Protein