Citations 20

DNAJC13 mutations in Parkinson disease

Human Molecular Genetics | November 12, 2013 | Volume: 23 | Issue: 7 | Pages: 1794-1801

10.1093/hmg/ddt570 | PMID 24218364

Abstract A Saskatchewan multi-incident family was clinically characterized with Parkinson disease (PD) and Lewy body pathology. PD segregates as an autosomal-dominant trait, which could not be ascribed to any known mutation. DNA from three affected members was subjected to exome sequencing. Genome alignment, variant annotation and comparative analyses were used to identify shared coding mutations. Sanger sequencing was performed within the extended family and ethnically matched controls. Subsequent genotyping was performed in a multi-ethnic case–control series consisting of 2928 patients and 2676 control subjects from Canada, Norway, Taiwan, Tunisia, and the USA. A novel mutation in receptor-mediated endocytosis 8/RME-8 (DNAJC13 p.Asn855Ser) was found to segregate with disease. Screening of cases and controls identified four additional patients with the mutation, of which two had familial parkinsonism. All carriers shared an ancestral DNAJC13 p.Asn855Ser haplotype and claimed Dutch–German–Russian Mennonite heritage. DNAJC13 regulates the dynamics of clathrin coats on early endosomes. Cellular analysis shows that the mutation confers a toxic gain-of-function and impairs endosomal transport. DNAJC13 immunoreactivity was also noted within Lewy body inclusions. In late-onset disease which is most reminiscent of idiopathic PD subtle deficits in endosomal receptor-sorting/recycling are highlighted by the discovery of pathogenic mutations VPS35, LRRK2 and now DNAJC13. With this latest discovery, and from a neuronal perspective, a temporal and functional ecology is emerging that connects synaptic exo- and endocytosis, vesicular trafficking, endosomal recycling and the endo-lysosomal degradative pathway. Molecular deficits in these processes are genetically linked to the phenotypic spectrum of parkinsonism associated with Lewy body pathology.
Anterior brain glucose hypometabolism predates dementia in progranulin mutation carriers

Neurology | September 5, 2013 | Volume: 81 | Issue: 15 | Pages: 1322-1331

10.1212/wnl.0b013e3182a8237e | PMID 24005336

Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)

Neurology | May 13, 2012 | Volume: 63 | Issue: 11 | Pages: 2165-2167

10.1212/01.wnl.0000145601.88274.88 | PMID 15596772

Autosomal dominant parkinsonism associated with variable synuclein and tau pathology

Neurology | May 13, 2012 | Volume: 62 | Issue: 9 | Pages: 1619-1622

10.1212/01.wnl.0000125015.06989.db | PMID 15136696

SCA-2 presenting as parkinsonism in an Alberta family

Neurology | May 13, 2012 | Volume: 59 | Issue: 10 | Pages: 1625-1627

10.1212/01.wnl.0000035625.19871.dc | PMID 12451209

PET studies of parkinsonism associated with mutation in the α-synuclein gene

Neurology | May 13, 2012 | Volume: 53 | Issue: 9 | Pages: 2097-2097

10.1212/wnl.53.9.2097 | PMID 10599788

The role of radiotracer imaging in Parkinson disease

Neurology | June 14, 2011 | Volume: 64 | Issue: 2 | Pages: 208-215

10.1212/01.wnl.0000149403.14458.7f | PMID 15668415

A family with parkinsonism, essential tremor, restless legs syndrome, and depression

Neurology | May 9, 2011 | Volume: 76 | Issue: 19 | Pages: 1623-1630

10.1212/wnl.0b013e318219fb42 | PMID 21555728

P2‐379: (18)F‐Fluorodeoxyglucose positron emission tomography in presymptomatic progranulin mutation carriers

Alzheimer's & Dementia | July 11, 2010 | Volume: 6 | Issue: 4S_Part_14 | Pages: No page available

10.1016/j.jalz.2010.05.1431

Progression of dopaminergic dysfunction in a LRRK2 kindred

Neurology | November 24, 2008 | Volume: 71 | Issue: 22 | Pages: 1790-1795

10.1212/01.wnl.0000335973.66333.58 | PMID 19029519