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PMID: 16997464 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural

Mutations in DJ-1 are rare in familial Parkinson disease.

Neuroscience letters ·Vol. 408 ·No. 3 ·2006-11-20 ·Pages 209-13

Pankratz N, Pauciulo MW, Elsaesser VE, Marek DK, Halter CA, Wojcieszek J, Rudolph A, Shults CW, Foroud T, Nichols WC, Parkinson Study Group - PROGENI Investigators

Abstract

Mutations in DJ-1 (PARK7) are one cause of early-onset autosomal-recessive parkinsonism. We screened for DJ-1 mutations in 93 affected individuals from the 64 multiplex Parkinson disease (PD) families in our sample that had the highest family-specific multipoint LOD scores at the DJ-1 locus. In addition to sequencing all coding exons for alterations, we used multiplex ligation-dependent probe amplification (MLPA) to examine the genomic copy number of DJ-1 exons. A known polymorphism (R98Q) was found in five PD subjects, once as a homozygote and in the other four cases as heterozygotes. No additional missense mutations and no exon deletions or duplications were detected. Our results, in combination with those of previous studies, suggest that alterations in DJ-1 are not a common cause of familial PD.

MeSH Terms
Aged Aged, 80 and over Arginine/genetics Exons Female Glutamic Acid/genetics Humans Intracellular Signaling Peptides and Proteins/genetics Lod Score Male Middle Aged Mutation/genetics Oncogene Proteins/genetics Parkinsonian Disorders/genetics Protein Deglycase DJ-1 RNA, Messenger/metabolism Reverse Transcriptase Polymerase Chain Reaction/methods
Chemicals
Intracellular Signaling Peptides and Proteins Oncogene Proteins RNA, Messenger Glutamic Acid Arginine PARK7 protein, human Protein Deglycase DJ-1
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Pankratz Nathan
Indiana University Medical Center, Indianapolis, IN, USA.
Pauciulo Michael W
Elsaesser Veronika E
Marek Diane K
Halter Cheryl A
Wojcieszek Joanne
Rudolph Alice
Shults Clifford W
Foroud Tatiana
Nichols William C
Parkinson Study Group - PROGENI Investigators
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Article Info
Journal
Neuroscience letters
Abbr.
Neurosci Lett
ISSN
0304-3940
Published
2006-11-20
Epub
2006-00-25
Pages
209-13
Language
English
Region
Ireland
NLM ID
7600130
PMCID
PMC1706076
Subset
IM
Grants
NINDS NIH HHS · R01 NS037167 · United States
NIA NIH HHS · U24 AG021886 · United States
NINDS NIH HHS · R01 NS37167 · United States
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