Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein.

Abstract

The Finnish variant late infantile neuronal ceroid lipofuscinosis (vLINCL) belongs to the neuronal ceroid lipofuscinosis group of common recessively inherited neurodegenerative disorders. The CLN 5 gene responsible for this brain disorder codes for a novel protein with no homology to previously reported proteins. In this study, we have investigated the biosynthesis and intracellular localization of this protein in transiently transfected BHK-21 cells using a CLN5-specific peptide antibody. Confocal immunofluorescence microscopy showed that wild-type CLN5 is predominantly targeted to lysosomes and immunoprecipitation analysis recognized a 60 kDa polypeptide. The molecular weight of this protein was reduced to 40 kDa by deglycosylation with Endo H and to 38 kDa with PNGase F. The same-sized glycosylated polypeptides were also observed in the media, suggesting that the 60 kDa glycosylated CLN5 polypeptide represents a soluble lysosomal glycoprotein, not an integral transmembrane protein as predicted earlier. The most common human vLINCL mutation blocked the lysosomal targeting of expressed polypeptides. This would imply that the pathogenesis of vLINCL would be associated with the defective lysosomal trafficking, preventing the normal biological function of the corresponding polypeptide.

• Authors: Juha Isosomppi, Jouni Vesa, Anu Jalanko, Leena Peltonen
• Journal: Human molecular genetics (Hum Mol Genet) Vol. 11 Issue 8 Pg. 885-91 (Apr 15 2002) ISSN: 0964-6906 [Print] England
• PMID: 11971870 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• CLN5 protein, human
• Lysosome-Associated Membrane Glycoproteins
• Membrane Proteins
• Cycloheximide

Topics

• Cell Line
• Cell-Free System
• Cycloheximide (metabolism)
• Humans
• Lysosome-Associated Membrane Glycoproteins
• Lysosomes (metabolism)
• Membrane Proteins (biosynthesis, metabolism)
• Neuronal Ceroid-Lipofuscinoses (etiology, genetics)
• Protein Processing, Post-Translational
• Protein Transport
• Sequence Analysis, Protein