Literature DB >> 16997464

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

Nathan Pankratz1, Michael W Pauciulo, Veronika E Elsaesser, Diane K Marek, Cheryl A Halter, Joanne Wojcieszek, Alice Rudolph, Clifford W Shults, Tatiana Foroud, William C Nichols.   

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.

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Year:  2006        PMID: 16997464      PMCID: PMC1706076          DOI: 10.1016/j.neulet.2006.09.003

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  24 in total

1.  DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex.

Authors:  Grazia Annesi; Giovanni Savettieri; Pierfrancesco Pugliese; Marco D'Amelio; Patrizia Tarantino; Paolo Ragonese; Vincenzo La Bella; Tommaso Piccoli; Donatella Civitelli; Ferdinanda Annesi; Brigida Fierro; Federico Piccoli; Gennarina Arabia; Manuela Caracciolo; Innocenza Claudia Cirò Candiano; Aldo Quattrone
Journal:  Ann Neurol       Date:  2005-11       Impact factor: 10.422

2.  [Mutation analysis of DJ1 gene in patients with autosomal recessive early-onset Parkinsonism].

Authors:  Ji-feng Guo; Bei-sha Tang; Yu-hu Zhang; Kun Xia; Fang Cai; Qian Pan; Lu Shen; Hong Jiang; Guo-hua Zhao; Xin-xiang Yan; Li Cao
Journal:  Zhonghua Yi Xue Yi Chuan Xue Za Zhi       Date:  2005-12

3.  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.

Authors:  Samer Karamohamed; L I Golbe; M H Mark; A M Lazzarini; O Suchowersky; N Labelle; Mark Guttman; L J Currie; G F Wooten; M Stacy; M Saint-Hilaire; R G Feldman; J Liu; C M Shoemaker; J B Wilk; A L DeStefano; J C Latourelle; G Xu; R Watts; J Growdon; M Lew; C Waters; P Vieregge; P P Pramstaller; C Klein; B A Racette; J S Perlmutter; A Parsian; Carlos Singer; E Montgomery; K Baker; J F Gusella; A Herbert; R H Myers
Journal:  Mov Disord       Date:  2005-09       Impact factor: 10.338

4.  Prevalence of parkinsonism and Parkinson's disease in Europe: the EUROPARKINSON Collaborative Study. European Community Concerted Action on the Epidemiology of Parkinson's disease.

Authors:  M C de Rijk; C Tzourio; M M Breteler; J F Dartigues; L Amaducci; S Lopez-Pousa; J M Manubens-Bertran; A Alpérovitch; W A Rocca
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-01       Impact factor: 10.154

Review 5.  Genetics of Parkinson's disease.

Authors:  Thomas Gasser
Journal:  Curr Opin Neurol       Date:  2005-08       Impact factor: 5.710

6.  Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.

Authors:  C M van Duijn; M C Dekker; V Bonifati; R J Galjaard; J J Houwing-Duistermaat; P J Snijders; L Testers; G J Breedveld; M Horstink; L A Sandkuijl; J C van Swieten; B A Oostra; P Heutink
Journal:  Am J Hum Genet       Date:  2001-07-02       Impact factor: 11.025

7.  Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases.

Authors:  A J Hughes; S E Daniel; L Kilford; A J Lees
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-03       Impact factor: 10.154

8.  PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism.

Authors:  Christine Klein; Ana Djarmati; Katja Hedrich; Nora Schäfer; Cesa Scaglione; Roberta Marchese; Norman Kock; Birgitt Schüle; Anja Hiller; Thora Lohnau; Susen Winkler; Karin Wiegers; Robert Hering; Peter Bauer; Olaf Riess; Giovanni Abbruzzese; Paolo Martinelli; Peter P Pramstaller
Journal:  Eur J Hum Genet       Date:  2005-09       Impact factor: 4.246

9.  Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism.

Authors:  Paul J Lockhart; Rebecca Bounds; Mary Hulihan; Jennifer Kachergus; Sarah Lincoln; Chin-Hsien Lin; Ruey-Meei Wu; Matthew J Farrer
Journal:  Mov Disord       Date:  2004-09       Impact factor: 10.338

10.  Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7).

Authors:  Robert Hering; Karsten M Strauss; Xiao Tao; Andreas Bauer; Dirk Woitalla; Eva-Maria Mietz; Slobodanka Petrovic; Peter Bauer; Wilhelm Schaible; Thomas Müller; Ludger Schöls; Christine Klein; Daniela Berg; Philipp T Meyer; Jörg B Schulz; Bernd Wollnik; Liang Tong; Rejko Krüger; Olaf Riess
Journal:  Hum Mutat       Date:  2004-10       Impact factor: 4.878

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  15 in total

Review 1.  Genetics of Parkinson's disease.

Authors:  Christine Klein; Ana Westenberger
Journal:  Cold Spring Harb Perspect Med       Date:  2012-01       Impact factor: 6.915

2.  Structural effects of Parkinson's disease linked DJ-1 mutations.

Authors:  Gaetano Malgieri; David Eliezer
Journal:  Protein Sci       Date:  2008-05       Impact factor: 6.725

Review 3.  Synaptic protein alterations in Parkinson's disease.

Authors:  Ilse S Pienaar; David Burn; Christopher Morris; David Dexter
Journal:  Mol Neurobiol       Date:  2011-12-29       Impact factor: 5.590

4.  Copy number variation in familial Parkinson disease.

Authors:  Nathan Pankratz; Alexandra Dumitriu; Kurt N Hetrick; Mei Sun; Jeanne C Latourelle; Jemma B Wilk; Cheryl Halter; Kimberly F Doheny; James F Gusella; William C Nichols; Richard H Myers; Tatiana Foroud; Anita L DeStefano
Journal:  PLoS One       Date:  2011-08-02       Impact factor: 3.240

Review 5.  Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance.

Authors:  Dena G Hernandez; Xylena Reed; Andrew B Singleton
Journal:  J Neurochem       Date:  2016-04-18       Impact factor: 5.372

6.  Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations.

Authors:  N Pankratz; D K Kissell; M W Pauciulo; C A Halter; A Rudolph; R F Pfeiffer; K S Marder; T Foroud; W C Nichols
Journal:  Neurology       Date:  2009-07-28       Impact factor: 9.910

Review 7.  Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.

Authors:  Karen Nuytemans; Jessie Theuns; Marc Cruts; Christine Van Broeckhoven
Journal:  Hum Mutat       Date:  2010-07       Impact factor: 4.878

8.  DJ-1 Mutations are Rare in a Swedish Parkinson Cohort.

Authors:  Anna Anvret; Jeff G Blackinton; Marie Westerlund; Caroline Ran; Olof Sydow; Thomas Willows; Anna Håkansson; Hans Nissbrandt; Andrea Carmine Belin
Journal:  Open Neurol J       Date:  2011-03-22

9.  DJ1 analysis in a large cohort of Italian early onset Parkinson Disease patients.

Authors:  Francesca Sironi; Paola Primignani; Sara Ricca; Sara Tunesi; Michela Zini; Silvana Tesei; Roberto Cilia; Gianni Pezzoli; Manuela Seia; Stefano Goldwurm
Journal:  Neurosci Lett       Date:  2013-10-28       Impact factor: 3.046

10.  Genetic insights into sporadic Parkinson's disease pathogenesis.

Authors:  Chou Chai; Kah-Leong Lim
Journal:  Curr Genomics       Date:  2013-12       Impact factor: 2.236

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