HIGH FUNCTIONING FRAGILE-X MALES - DEMONSTRATION OF AN UNMETHYLATED FULLY EXPANDED FMR-1 MUTATION ASSOCIATED WITH PROTEIN EXPRESSION

被引:176
作者
HAGERMAN, RJ
HULL, CE
SAFANDA, JF
CARPENTER, I
STALEY, LW
OCONNOR, RA
SEYDEL, C
MAZZOCCO, MMM
SNOW, K
THIBODEAU, SN
KUHL, D
NELSON, DL
CASKEY, CT
TAYLOR, AK
机构
[1] UNIV COLORADO,HLTH SCI CTR,DEPT PEDIAT,DENVER,CO 80262
[2] UNIV COLORADO,HLTH SCI CTR,DNA DIAGNOST LAB,DENVER,CO
[3] MAYO CLIN & MAYO FDN,MOLEC GENET LAB,ROCHESTER,MN
[4] BAYLOR COLL MED,INST MOLEC GENET,HOUSTON,TX 77030
[5] BAYLOR COLL MED,HOWARD HUGHES MED INST,HOUSTON,TX
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1994年 / 51卷 / 04期
关键词
FRAGILE X SYNDROME; MARTIN-BELL SYNDROME; FMR-1; GENE; METHYLATION; MOSAIC; HIGH FUNCTIONING;
D O I
10.1002/ajmg.1320510404
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Fragile X (fra(X)) males with a standardized IQ score of 70 or higher represent a high functioning (HF) or nonretarded fra(X) male group. This group, which does not include nonpenetrant males, has received little research attention to date. Of 221 fra(X) males who had been evaluated through The Children's Hospital in Denver since 1981 and had completed cognitive or developmental testing, 29 (13%) were high functioning by the above definition. We found that HF males on the whole had a lower cytogenetic score and were younger than retarded fra(X) males, but there was no difference between these two groups in the number of typical fra(X) physical manifestations present. FMR-1 DNA testing was performed on 134 fra(X) males and methylation status was determined for 51 of these. A greater percentage of HF males had a mosaic pattern or an incompletely methylated full mutation than did retarded males. A unique DNA pattern, an unmethylated fully expanded mutation, was discovered in 3 of the highest functioning fra(X) males. Protein studies performed on 2 of these males demonstrated the presence of FMR-1 protein, albeit at lower levels than normal. FMR-1 protein was not present in retarded fra(X) males. Significant FMR-1 protein expression may be responsible for higher cognitive functioning in the 2 males with unmethylated fully expanded mutations compared to retarded fra(X) males. (C) 1994 Wiley-Liss, Inc.,Inc.
引用
收藏
页码:298 / 308
页数:11
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