| Literature DB >> 21545838 |
Reena Prity Murmu1, Elodie Martin, Agnès Rastetter, Typhaine Esteves, Marie-Paule Muriel, Khalid Hamid El Hachimi, Paola Silvia Denora, Aurélien Dauphin, José Carlos Fernandez, Charles Duyckaerts, Alexis Brice, Frédéric Darios, Giovanni Stevanin.
Abstract
Truncating mutations in the SPG11 and SPG15 genes cause complicated spastic paraplegia, severe neurological conditions due to loss of the functions of spatacsin and spastizin, respectively. We developed specific polyclonal anti-spatacsin (SPG11) and anti-spastizin (SPG15) antisera, which we then used to explore the intracellular and tissue localizations of these proteins. We observed expression of both proteins in human and rat central nervous system, which was particularly strong in cortical and spinal motor neurons as well as in retina. Both proteins were also expressed ubiquitously and strongly in embryos. In cultured cells, these two proteins had similar diffuse punctate, cytoplasmic and sometimes nuclear (spastizin) distributions. They partially co-localized with multiple organelles, particularly with protein-trafficking vesicles, endoplasmic reticulum and microtubules. Spastizin was also found at the mitochondria surface. This first study of the endogenous expression of spatacsin and spastizin shows similarities in their expression patterns that could account for their overlapping clinical phenotypes and involvement in a common protein complex.Entities:
Mesh:
Substances:
Year: 2011 PMID: 21545838 DOI: 10.1016/j.mcn.2011.04.004
Source DB: PubMed Journal: Mol Cell Neurosci ISSN: 1044-7431 Impact factor: 4.314