Insights into Lafora disease: malin is an E3 ubiquitin ligase that ubiquitinates and promotes the degradation of laforin.

Abstract

Lafora disease (LD) is a fatal form of progressive myoclonus epilepsy caused by recessive mutations in either a gene encoding a dual-specificity phosphatase, known as laforin, or a recently identified gene encoding the protein known as malin. Here, we demonstrate that malin is a single subunit E3 ubiquitin (Ub) ligase and that its RING domain is necessary and sufficient to mediate ubiquitination. Additionally, malin interacts with and polyubiquitinates laforin, leading to its degradation. Missense mutations in malin that are present in LD patients abolish its ability to polyubiquitinate and signal the degradation of laforin. Our results demonstrate that laforin is a physiologic substrate of malin, and we propose possible models to explain how recessive mutations in either malin or laforin result in LD. Furthermore, these data distinguish malin as an E3 Ub ligase whose activity is necessary to prevent a neurodegenerative disease that involves formation of nonproteinacious inclusion bodies.

• Authors: Matthew S Gentry, Carolyn A Worby, Jack E Dixon
• Journal: Proceedings of the National Academy of Sciences of the United States of America (Proc Natl Acad Sci U S A) Vol. 102 Issue 24 Pg. 8501-6 (Jun 14 2005) ISSN: 0027-8424 [Print] United States
• PMID: 15930137 (Publication Type: Comparative Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Carrier Proteins
• NHLRC1 protein, human
• Ubiquitin-Protein Ligases
• Protein Tyrosine Phosphatases
• Protein Tyrosine Phosphatases, Non-Receptor
• EPM2A protein, human

Topics

• Carrier Proteins (genetics, metabolism)
• Cell Line
• Humans
• Immunoprecipitation
• Lafora Disease (metabolism)
• Models, Biological
• Mutation, Missense (genetics)
• Plasmids (genetics)
• Protein Binding
• Protein Tyrosine Phosphatases (metabolism)
• Protein Tyrosine Phosphatases, Non-Receptor
• Transfection
• Two-Hybrid System Techniques
• Ubiquitin-Protein Ligases (metabolism)