Clinical, Neuropathological, and Biochemical Characterization of the Novel Tau Mutation P332S

Article type: Research Article

Authors: Deramecourt, Vincent^{a; b; c; d} | Lebert, Florence^{a; c} | Maurage, Claude-Alain^{a; b; d} | Fernandez-Gomez, Francisco-Jose^{a; b} | Dujardin, Simon^{a; b} | Colin, Morvane^{a; b} | Sergeant, Nicolas^{a; b} | Buée-Scherrer, Valérie^{a; b} | Clot, Fabienne^e | Ber, Isabelle Le^{f; g; h} | Brice, Alexis^{e; f; g; h} | Pasquier, Florence^{a; c} | Buée, Luc^{a; b; *}

Affiliations: [a] Univ Lille Nord de France, UDSL, Lille, France | [b] INSERM U837, JPARC, Lille, France | [c] CHU Lille, Memory Clinic, Lille, France | [d] CHU Lille, Department of Pathology, Lille, France | [e] Department of Genetics and Cytogenetics, AP-HP, Pitié-Salpêtrière Hospital, Paris, France | [f] CR-ICM UMRS9750, Paris, France | [g] INSERM U975, Paris, France | [h] Department of Neurology, AP-HP, Pitié-Salpêtrière Hospital, Paris, France

Correspondence: [*] Correspondence to: Luc Buée, INSERM U837, Centre de Recherche Jean-Pierre Aubert, 1 place de Verdun, Lille Cedex 59045, France. Tel.: +33 320 29 88 66; Fax: +33 320 53 85 62; E-mail: [email protected].

Abstract: MAPT mutations cause autosomal dominant frontotemporal lobar degeneration. These diseases are characterized by considerable heterogeneity in their clinical, neuropathological, and biochemical presentations. We describe the full characterization of a family with autosomal dominant frontotemporal lobar degeneration caused by a novel MAPT mutation. Clinical, imaging, neuropathological, and biochemical data are presented. The proband was a woman who died at 85 years old, 25 years after the onset of a slowly progressive and isolated anarthria and opercular syndrome. The pathological examination of her brain showed marked atrophy of primary motor and premotor cortices, associated with predominant neuronal tau-positive lesions mimicking Pick bodies. At the biochemical level, the six tau isoforms aggregate to display a pathological triplet at 60, 64, and 69 kDa. Two of her sons presented at 48 and 50 years old with a right temporal variant of frontotemporal degeneration characterized by severe prosopagnosia, semantic impairment, and behavioral modifications. In these three patients, the molecular analysis of MAPT showed the c.1945C>T mutation on exon 11 resulting in the P332S substitution in tau sequence. This mutation changes the PGGG motif of the third repeat domain of the protein and therefore reduces the ability of tau to bind microtubule. From a clinical point of view, this mutation is associated with considerable intrafamilial phenotypic variation.

Keywords: Frontotemporal lobar degeneration, FTDP-17, MAPT, Pick body, progressive anarthria, semantic dementia, tau protein

DOI: 10.3233/JAD-2012-120160

Journal: Journal of Alzheimer's Disease, vol. 31, no. 4, pp. 741-749, 2012