TRINUCLEOTIDE REPEAT AMPLIFICATION AND HYPERMETHYLATION OF A CPG ISLAND IN FRAXE MENTAL-RETARDATION

被引:508
作者
KNIGHT, SJL
FLANNERY, AV
HIRST, MC
CAMPBELL, L
CHRISTODOULOU, Z
PHELPS, SR
POINTON, J
MIDDLETONPRICE, HR
BARNICOAT, A
PEMBREY, ME
HOLLAND, J
OOSTRA, BA
BOBROW, M
DAVIES, KE
机构
[1] INST CHILD HLTH,LONDON WC1N 1EH,ENGLAND
[2] UNITED MED & DENT SCH GUYS & ST THOMAS HOSP,DIV MED & MOLEC GENET,LONDON SE1 9RT,ENGLAND
[3] ERASMUS UNIV ROTTERDAM,DEPT CLIN GENET,3000 DR ROTTERDAM,NETHERLANDS
基金
英国惠康基金;
关键词
D O I
10.1016/0092-8674(93)90300-F
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
We have cloned the fragile site FRAXE and demonstrate that individuals with this fragile site possess amplifications of a GCC repeat adjacent to a CpG island in Xq28 of the human X chromosome. Normal individuals have 6-25 copies of the GCC repeat, whereas mentally retarded, FRAXE-positive individuals have >200 copies and also have methylation at the CpG island. This situation is similar to that seen at the FRAXA locus and is another example in which a trinucleotide repeat expansion is associated with a human genetic disorder. In contrast with the fragile X syndrome, the GCC repeat can expand or contract and is equally unstable when passed through the male or female line. These results also have implications for the understanding of chromosome fragility.
引用
收藏
页码:127 / 134
页数:8
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