Isoform-specific increase of spastin stability by N-terminal missense variants including intragenic modifiers of SPG4 hereditary spastic paraplegia

Authors: Schickel, J.1; Pamminger, T.1; Ehrsam, A.1; Münch, S.2; Huang, X.3; Klopstock, T.4; Kurlemann, G.5; Hemmerich, P.2; Dubiel, W.3; Deufel, T.1; Beetz, C.1

Source: European Journal of Neurology, Volume 14, Number 12, December 2007 , pp. 1322-1328(7)

Publisher: Blackwell Publishing

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Abstract:

Hereditary spastic paraplegia (HSP) is a neurodegenerative disorder selectively affecting axons of spinal cord motoneurons. Classical mutations in the most frequent HSP gene SPAST (spastin protein) act through haploinsufficiency by abolishing the activity of a C-terminal ATPase domain or by interfering with expression from the affected allele. N-terminal missense variants have been suggested to represent rare polymorphisms, to cause unusually mild phenotypes, and to aggravate the effect of a classical mutation. We confirm these associations for p.S44L but do not detect two other variants (p.E43Q; p.P45Q) in HSP patients and controls. We show that neither of several disease mechanisms associated with classical SPAST mutations applies to the N-terminal variants. Instead, all three alterations enhance the stability of one of two alternative spastin isoforms. Their phenotypic effect may thus not be mediated by haploinsufficiency but by increasing isoform competition for interacting proteins, substrates or oligomerization partners.

Keywords: hereditary spastic paraplegia; modifiers; neurodegeneration; PEST sequence; polymorphism; protein stability; SPAST; spastin

Document Type: Research article

DOI: 10.1111/j.1468-1331.2007.01971.x

Affiliations: 1: Institut für Klinische Chemie und Laboratoriumsdiagnostik, Universitätsklinikum, Jena, Germany 2: Leibniz Institut für Altersforschung - Fritz-Lipmann-Institut, Jena, Germany 3: Abteilung Molekularbiologie der Chirurgischen Klinik, Charité, Berlin, Germany 4: Neurologische Klinik, Klinikum Großhadern, München, Germany 5: Abteilung Neuropädiatrie, Kinderhospital der Universität, Münster, Germany

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