Congenital ovine neuronal ceroid lipofuscinosis - A cathepsin D deficiency with increased levels of the inactive enzyme

J. Tyynelä, I. Sohar, D. E. Sleat, R. M. Gin, R. J. Don Nelly, M. Baumann, M. Haltia, P. Lobel

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

We recently showed that a form of neuronal ceroid lipofuscinosis (NCL) in white Swedish landrace sheep is caused by a missense mutation in the cathepsin D gene resulting in complete inactivation of the enzyme. Despite the lack of cathepsin D activity, the brains of the cathepsin D deficient sheep showed strongly increased staining for cathepsin D in immunohistochemistry. By Western blotting, a 5-10 fold increase in the level of cathepsin D was confirmed. These results indicate that the missense mutation in congenital NCL sheep results in the synthesis of an inactive yet stable cathepsin D.

Original languageEnglish (US)
Article number05800091
Pages (from-to)43-45
Number of pages3
JournalEuropean Journal of Paediatric Neurology
Volume5
DOIs
StatePublished - 2001

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health
  • Clinical Neurology

Keywords

  • Cathepsin D
  • Enzyme deficiency
  • Lysosomal storage
  • Neurodegeneration
  • Neuronal ceroid lipofuscinosis

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