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
References (24)
24 references, click to expand
-
Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7).
Hum Mutat. 2004 Oct;24(4):321-9
PMID: 15365989
-
Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism.
Mov Disord. 2004 Sep;19(9):1065-9
PMID: 15372597
-
Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases.
J Neurol Neurosurg Psychiatry. 1992 Mar;55(3):181-4
PMID: 1564476
-
Prevalence of parkinsonism and Parkinson's disease in Europe: the EUROPARKINSON Collaborative Study. European Community Concerted Action on the Epidemiology of Parkinson's disease.
J Neurol Neurosurg Psychiatry. 1997 Jan;62(1):10-5
PMID: 9010393
-
Genetics of Parkinson's disease.
Curr Opin Neurol. 2005 Aug;18(4):363-9
PMID: 16003110
-
PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism.
Eur J Hum Genet. 2005 Sep;13(9):1086-93
PMID: 15970950
-
Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study.
Mov Disord. 2005 Sep;20(9):1188-91
PMID: 15966003
-
DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex.
Ann Neurol. 2005 Nov;58(5):803-7
PMID: 16240358
-
[Mutation analysis of DJ1 gene in patients with autosomal recessive early-onset Parkinsonism].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Dec;22(6):641-3
PMID: 16331561
-
Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.
Am J Hum Genet. 2001 Sep;69(3):629-34
PMID: 11462174
-
What features improve the accuracy of clinical diagnosis in Parkinson's disease: a clinicopathologic study. 1992.
Neurology. 2001 Nov;57(10 Suppl 3):S34-8
PMID: 11775598
-
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism.
Science. 2003 Jan 10;299(5604):256-9
PMID: 12446870
-
Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease.
Neurology. 2003 Mar 11;60(5):796-801
PMID: 12629236
-
Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.
Ann Neurol. 2003 Aug;54(2):271-4
PMID: 12891685
-
The role of pathogenic DJ-1 mutations in Parkinson's disease.
Ann Neurol. 2003 Sep;54(3):283-6
PMID: 12953260
-
Screening for DJ-1 mutations in early onset autosomal recessive parkinsonism.
Neurology. 2003 Nov 25;61(10):1429-31
PMID: 14638971
-
The R98Q variation in DJ-1 represents a rare polymorphism.
Ann Neurol. 2004 Jan;55(1):145; author reply 145-6
PMID: 14705128
-
DJ-1 mutations in Parkinson's disease.
J Neurol Neurosurg Psychiatry. 2004 Jan;75(1):144-5
PMID: 14707326
-
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.
Neurology. 2004 Feb 10;62(3):389-94
PMID: 14872018
-
DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function.
J Med Genet. 2004 Mar;41(3):e22
PMID: 14985393
-
Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients.
Hum Mutat. 2004 May;23(5):525
PMID: 15108293
-
Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel loci.
Neurology. 2004 May 11;62(9):1616-8
PMID: 15136695
-
Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations.
Mov Disord. 2004 Jul;19(7):796-800
PMID: 15254937
-
Genetic analysis of DJ-1 in a cohort Parkinson's disease patients of different ethnicity.
Neurosci Lett. 2004 Aug 26;367(1):109-12
PMID: 15308309