Reference : Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7).
Scientific journals : Article
Life sciences : Genetics & genetic processes
http://hdl.handle.net/10993/17140
Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7).
English
Hering, Robert [> >]
Strauss, Karsten M. [> >]
Tao, Xiao [> >]
Bauer, Andreas [> >]
Woitalla, Dirk [> >]
Mietz, Eva-Maria [> >]
Petrovic, Slobodanka [> >]
Bauer, Peter [> >]
Schaible, Wilhelm [> >]
Muller, Thomas [> >]
Schols, Ludger [> >]
Klein, Christine [> >]
Berg, Daniela [> >]
Meyer, Philipp T. [> >]
Schulz, Jorg B. [> >]
Wollnik, Bernd [> >]
Tong, Liang [> >]
Krüger, Rejko mailto [University of Luxembourg > Faculty of Science, Technology and Communication (FSTC) > Life Science Research Unit]
Riess, Olaf [> >]
2004
Human mutation
24
4
321-9
Yes (verified by ORBilu)
1059-7794
1098-1004
United States
[en] Adult ; Age of Onset ; Amino Acid Substitution ; Animals ; COS Cells ; Cell Line/metabolism ; Cell Nucleus/chemistry ; Cercopithecus aethiops ; Corpus Striatum/metabolism/radionuclide imaging ; Crystallography, X-Ray ; DNA Mutational Analysis ; Dopamine/metabolism ; Dopamine Plasma Membrane Transport Proteins ; Female ; Genetic Heterogeneity ; Genetic Testing ; Genotype ; Germany/epidemiology ; Humans ; Intracellular Signaling Peptides and Proteins ; Kidney ; Male ; Membrane Glycoproteins/metabolism ; Membrane Transport Proteins/metabolism ; Middle Aged ; Models, Molecular ; Mutation, Missense ; Nerve Tissue Proteins/metabolism ; Oncogene Proteins/analysis/biosynthesis/chemistry/genetics ; Parkinson Disease/epidemiology/genetics/radionuclide imaging ; Pedigree ; Point Mutation ; Positron-Emission Tomography ; Protein Conformation ; Recombinant Fusion Proteins/analysis/biosynthesis ; Turkey/ethnology
[en] Mutations in the parkin gene have been identified as a common cause of autosomal recessive inherited Parkinson disease (PD) associated with early disease manifestation. However, based on linkage data, mutations in other genes contribute to the genetic heterogeneity of early-onset PD (EOPD). Recently, two mutations in the DJ1 gene were described as a second cause of autosomal recessive EOPD (PARK7). Analyzing the PARK7/DJ1 gene in 104 EOPD patients, we identified a third mutation, c.192G>C (p.E64D), associated with EOPD in a patient of Turkish ancestry and characterized the functional significance of this amino acid substitution. In the patient, a substantial reduction of dopamine uptake transporter (DAT) binding was found in the striatum using [(18)F]FP-CIT and PET, indicating a serious loss of presynaptic dopaminergic afferents. His sister, homozygous for E64D, was clinically unaffected but showed reduced dopamine uptake when compared with a clinically unaffected brother, who is heterozygous for E64D. We demonstrate by crystallography that the E64D mutation does not alter the structure of the DJ1 protein, however we observe a tendency towards decreased levels of the mutant protein when overexpressed in HEK293 or COS7 cells. Using immunocytochemistry in contrast to the homogenous nuclear and cytoplasmic staining in HEK293 cells overexpressing wild-type DJ1, about 5% of the cells expressing E64D and up to 80% of the cells expressing the recently described L166P mutation displayed a predominant nuclear localization of the mutant DJ1 protein.
Luxembourg Centre for Systems Biomedicine (LCSB): Clinical & Experimental Neuroscience (Krüger Group)
http://hdl.handle.net/10993/17140
10.1002/humu.20089
Copyright 2004 Wiley-Liss, Inc.

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