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Structural and molecular insights into the mechanism of action of human angiogenin-ALS variants in neurons.

Nature communications | 2012

Mutations in angiogenin (ANG), a member of the ribonuclease A superfamily, are associated with amyotrophic lateral sclerosis (ALS; sporadic and familial) and Parkinson's disease. We have previously shown that ANG is expressed in neurons during neuro-ectodermal differentiation, and that it has both neurotrophic and neuroprotective functions. Here we report the atomic resolution structure of native ANG and 11 ANG-ALS variants. We correlate the structural changes to the effects on neuronal survival and the ability to induce stress granules in neuronal cell lines. ANG-ALS variants that affect the structure of the catalytic site and either decrease or increase the RNase activity affect neuronal survival. Neuronal cell lines expressing the ANG-ALS variants also lack the ability to form stress granules. Our structure-function studies on these ANG-ALS variants are the first to provide insights into the cellular and molecular mechanisms underlying their role in ALS.

Pubmed ID: 23047679 RIS Download

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Associated grants

  • Agency: Medical Research Council, United Kingdom
  • Agency: Wellcome Trust, United Kingdom
    Id: 088464
  • Agency: Wellcome Trust, United Kingdom
    Id: 083191
  • Agency: Wellcome Trust, United Kingdom
  • Agency: National Centre for the Replacement, Refinement and Reduction of Animals in Research, United Kingdom
    Id: G0900786/1

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RRID:SCR_014224

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RRID:SCR_014226

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