Microsatellite repeat instability and neurological disease

被引:94
作者
Brouwer, Judith R. [1 ]
Willemsen, Rob [1 ]
Oostra, Ben A. [1 ]
机构
[1] ErasmusMC, Dept Clin Genet, NL-3000 CA Rotterdam, Netherlands
关键词
microsatellite instability; neurological disease; repeat instability; trinucleotide repeat; FRAGILE-X PREMUTATION; MYOTONIC-DYSTROPHY; TRINUCLEOTIDE REPEAT; CTG REPEAT; DROSOPHILA MODEL; CGG-REPEAT; FULL MUTATION; MEDIATED NEURODEGENERATION; INTRANUCLEAR INCLUSIONS; TREMOR/ATAXIA SYNDROME;
D O I
10.1002/bies.080122
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
Over 20 unstable microsatellite repeats have been identified as the cause of neurological disease in humans. The repeat nucleotide sequences, their location within the genes, the ranges of normal and disease-causing repeat length and the clinical outcomes differ. Unstable repeats can be located in the coding or the non-coding region of a gene. Different pathogenic mechanisms that are hypothesised to underlie the diseases are discussed. Evidence is given both from studies in simple model systems and from studies on human material and in animal models. Since somatic instability might affect the clinical outcome, this is briefly touched on. Available data and theories on the timing and mechanisms of the repeat instability itself are discussed, along with factors that have been observed to affect instability. Finally, the question of why the often harmful unstable repeats have been maintained throughout evolution is addressed.
引用
收藏
页码:71 / 83
页数:13
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