Laforin is required for the functional activation of malin in endoplasmic reticulum stress resistance in neuronal cells.

Abstract

Mutations in either EPM2A, the gene encoding a dual-specificity phosphatase named laforin, or NHLRC1, the gene encoding an E3 ubiquitin ligase named malin, cause Lafora disease in humans. Lafora disease is a fatal neurological disorder characterized by progressive myoclonus epilepsy, severe neurological deterioration and accumulation of poorly branched glycogen inclusions, called Lafora bodies or polyglucosan bodies, within the cell cytoplasm. The molecular mechanism underlying the neuropathogenesis of Lafora disease remains unknown. Here, we present data demonstrating that in the cells expressing low levels of laforin protein, overexpressed malin and its Lafora disease-causing missense mutants are stably polyubiquitinated. Malin and malin mutants form ubiquitin-positive aggregates in or around the nuclei of the cells in which they are expressed. Neither wild-type malin nor its mutants elicit endoplasmic reticulum stress, although the mutants exaggerate the response to endoplasmic reticulum stress. Overexpressed laforin impairs the polyubiquitination of malin while it recruits malin to polyglucosan bodies. The recruitment and activities of laforin and malin are both required for the polyglucosan body disruption. Consistently, targeted deletion of laforin in brain cells from Epm2a knockout mice increases polyubiquitinated proteins. Knockdown of Epm2a or Nhlrc1 in neuronal Neuro2a cells shows that they cooperate to allow cells to resist ER stress and apoptosis. These results reveal that a functional laforin-malin complex plays a critical role in disrupting Lafora bodies and relieving ER stress, implying that a causative pathogenic mechanism underlies their deficiency in Lafora disease.

• Authors: Li Zeng, Yin Wang, Otto Baba, Pan Zheng, Yang Liu, Yan Liu
• Journal: The FEBS journal (FEBS J) Vol. 279 Issue 14 Pg. 2467-78 (Jul 2012) ISSN: 1742-4658 [Electronic] England
• PMID: 22578008 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
• Copyright: © 2012 The Authors Journal compilation © 2012 FEBS.

Chemical References

• Glucans
• Polyubiquitin
• polyglucosan
• NHLRC1 protein, mouse
• Ubiquitin-Protein Ligases
• Dual-Specificity Phosphatases
• Epm2a protein, mouse
• Protein Tyrosine Phosphatases, Non-Receptor

Topics

• Animals
• Blotting, Western
• Cell Line, Tumor
• Dual-Specificity Phosphatases (genetics, metabolism)
• Endoplasmic Reticulum Stress
• Female
• Glucans (metabolism)
• HEK293 Cells
• Humans
• Immunoprecipitation
• Inclusion Bodies (genetics, metabolism)
• Lafora Disease (genetics, metabolism)
• Male
• Mice
• Mice, 129 Strain
• Mice, Inbred C57BL
• Mice, Knockout
• Mutation
• Neurons (metabolism)
• Polyubiquitin (metabolism)
• Protein Binding
• Protein Tyrosine Phosphatases, Non-Receptor
• Ubiquitin-Protein Ligases (genetics, metabolism)