Somatic mutation: a cause of sporadic neurodegenerative diseases?

被引:24
作者
Pamphlett, R [1 ]
机构
[1] Univ Sydney, Dept Pathol, Sydney, NSW 2006, Australia
关键词
D O I
10.1016/j.mehy.2003.11.023
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The major causes of the common neurodegenerative diseases remain unknown. Alzheimer's disease, Parkinson's disease and motor neuron disease occur in both sporadic and familial forms, and mutations are progressively being found in families with these disorders. However, attempts to find causative mutations in blood DNA from the sporadic forms of the diseases have proved fruitless. It is hypothesised that this is because the causative mutations are found only in the cells in the central nervous system that are affected by the disease. These mutations arise in the developing embryo in progenitor cells of neurons or glia. The diseases are not passed to offspring since the mutations are not present in the germ-line. To find somatic mutations, the affected central nervous system cells need to be separated out and submitted to DNA analysis. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:679 / 682
页数:4
相关论文
共 19 条
[1]   Detection and cellular localization of enterovirus RNA sequences in spinal cord of patients with ALS [J].
Berger, MM ;
Kopp, N ;
Vital, C ;
Redl, B ;
Aymard, M ;
Lina, B .
NEUROLOGY, 2000, 54 (01) :20-25
[2]  
Broo AE, 2001, WA SCI TECHNOL, V1, P19
[3]   Parkinson's disease: piecing together a genetic jigsaw [J].
Dekker, MCJ ;
Bonifati, V ;
van Duijn, CM .
BRAIN, 2003, 126 :1722-1733
[4]   Laser capture microdissection [J].
EmmertBuck, MR ;
Bonner, RF ;
Smith, PD ;
Chuaqui, RF ;
Zhuang, ZP ;
Goldstein, SR ;
Weiss, RA ;
Liotta, LA .
SCIENCE, 1996, 274 (5289) :998-1001
[5]   Somatic gene mutation and human disease other than cancer [J].
Erickson, RP .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2003, 543 (02) :125-136
[6]   The use of denaturing high-performance liquid chromatography (DHPLC) for the analysis of genetic variations: Impact for diagnostics and pharmacogenetics [J].
Frueh, FW ;
Noyer-Weidner, M .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2003, 41 (04) :452-461
[7]  
LAMBRECHTS D, 2003, NAT GENET, V54, P507
[8]   Accumulation of SOD1 mutants in postnatal motoneurons does not cause motoneuron pathology or motoneuron disease [J].
Lino, MM ;
Schneider, C ;
Caroni, P .
JOURNAL OF NEUROSCIENCE, 2002, 22 (12) :4825-4832
[9]   Familial aggregation of early- and late-onset Parkinson's disease [J].
Marder, K ;
Levy, G ;
Louis, ED ;
Mejia-Santana, H ;
Cote, L ;
Andrews, H ;
Harris, J ;
Waters, C ;
Ford, B ;
Frucht, S ;
Fahn, S ;
Ottman, R .
ANNALS OF NEUROLOGY, 2003, 54 (04) :507-513
[10]   Parkinson's disease, pesticides, and glutathione transferase polymorphisms [J].
Menegon, A ;
Board, PG ;
Blackburn, AC ;
Mellick, GD ;
Le Couteur, DG .
LANCET, 1998, 352 (9137) :1344-1346