Murray A, Macpherson J N, Pound M C, Sharrock A, Youings S A, Dennis N R, McKechnie N, Linehan P, Morton N E, Jacobs P A
Wessex Regional Genetics Laboratory, Salisbury District Hospital, Wiltshire, UK.
Hum Mol Genet. 1997 Feb;6(2):173-84. doi: 10.1093/hmg/6.2.173.
Factors involved in the stability of trinucleotide repeats during transmission were studied in 139 families in which a full mutation, premutation or intermediate allele at either FRAXA or FRAXE was segregating. The transmission of alleles at FRAXA, FRAXE and four microsatellite loci were recorded for all individuals. Instability within the minimal and common ranges (0-40 repeats for FRAXA, 0-30 repeats for FRAXE) was extremely rare; only one example was observed, an increased in size at FRAXA from 29 to 39 repeats. Four FRAXA and three FRAXE alleles in the intermediate range (41-60) repeats for FRAXA, 31-60 for FRAXE) were unstably transmitted. Instability was more frequent for FRAXA intermediate alleles that had a tract of pure CGG greater than 37 although instability only occurred in two of 13 such transmissions: the changes observed were limited to only one or two repeats. Premutation FRAXA alleles over 100 repeats expanded to a full mutation during female transmission in 100% of cases, in agreement with other published series. There was no clear correlation between haplotype and probability of expansion of FRAXA premutations. Instability at FRAXA or FRAXE was more often observed in conjunction with a second instability at an independent locus suggesting genomic instability as a possible mechanism by which at least some FRAXA and FRAXE mutations arise.
在139个家系中研究了三核苷酸重复序列在传递过程中的稳定性相关因素,这些家系中FRAXA或FRAXE位点存在全突变、前突变或中间等位基因的分离现象。记录了所有个体在FRAXA、FRAXE和四个微卫星位点上等位基因的传递情况。在最小和常见范围内(FRAXA为0 - 40次重复,FRAXE为0 - 30次重复)的不稳定性极为罕见;仅观察到一个例子,FRAXA处的大小从29次重复增加到39次重复。四个FRAXA和三个FRAXE中间范围(FRAXA为41 - 60次重复,FRAXE为31 - 60次重复)的等位基因传递不稳定。对于具有大于37个纯CGG片段的FRAXA中间等位基因,不稳定性更为频繁,尽管在13次此类传递中仅发生了两次:观察到的变化仅限于一两个重复。超过100次重复的FRAXA前突变等位基因在女性传递过程中100%扩展为全突变,这与其他已发表的系列研究结果一致。单倍型与FRAXA前突变扩展概率之间没有明显的相关性。在FRAXA或FRAXE处的不稳定性更常与独立位点的第二次不稳定性同时出现,这表明基因组不稳定性可能是至少一些FRAXA和FRAXE突变产生的一种机制。