Analysis of mitochondrial targeting sequence and coding region polymorphisms of the manganese superoxide dismutase gene in German Parkinson disease patients

被引:64
作者
Grasbon-Frodl, EM
Kösel, S
Riess, O
Müller, U
Mehraein, P
Graeber, MB
机构
[1] Max Planck Inst Neurobiol, Dept Neuromorphol, Mol Neuropathol Lab, D-85152 Martinsried, Germany
[2] Univ Munich, Inst Neuropathol, Mol Neuropathol Lab, D-80337 Munich, Germany
[3] Ruhr Univ Bochum, Dept Human Mol Genet, D-44780 Bochum, Germany
[4] Univ Giessen, Inst Human Genet, D-35392 Giessen, Germany
关键词
mitochondria; mitochondrial targeting sequence; MnSOD; Parkinson disease;
D O I
10.1006/bbrc.1998.9998
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two polymorphisms of the MnSOD gene, Ile58Thr and Ala9Val, have been associated with Parkinson disease (PD). The Ile58Thr amino acid exchange affects the stability at the tetrameric interface of the enzyme and reduces the enzymatic activity of MnSOD while the Ala/Val substitution at position -9 of the mitochondrial targeting sequence (TIS) may lead to misdirected intracellular trafficking. We have analyzed 63 German Caucasian PD patients for possible sequence variation in the MTS as well as in exon 3 of the MnSOD gene. All 63 PD patients analyzed exhibited a T at nucleotide position 5777 in exon 3 of the MnSOD gene corresponding to ATA, or ne at the peptide level, and no other sequence variants were found In addition, both alleles of the Ala9Val polymorphism in the MTS of MnSOD were equally distributed between German PD patients and controls excluding this gene variant as a risk factor for PD in caucasian subjects. (C) 1999 Academic Press.
引用
收藏
页码:749 / 752
页数:4
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