Nolin Sarah L, Glicksman Anne, Tortora Nicole, Allen Emily, Macpherson James, Mila Montserrat, Vianna-Morgante Angela M, Sherman Stephanie L, Dobkin Carl, Latham Gary J, Hadd Andrew G
Department of Human Genetics, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, New York.
Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia.
Am J Med Genet A. 2019 Jul;179(7):1148-1156. doi: 10.1002/ajmg.a.61165. Epub 2019 May 2.
Instability of the FMR1 repeat, commonly observed in transmissions of premutation alleles (55-200 repeats), is influenced by the size of the repeat, its internal structure and the sex of the transmitting parent. We assessed these three factors in unstable transmissions of 14/3,335 normal (~5 to 44 repeats), 54/293 intermediate (45-54 repeats), and 1561/1,880 premutation alleles. While most unstable transmissions led to expansions, contractions to smaller repeats were observed in all size classes. For normal alleles, instability was more frequent in paternal transmissions and in alleles with long 3' uninterrupted repeat lengths. For premutation alleles, contractions also occurred more often in paternal than maternal transmissions and the frequency of paternal contractions increased linearly with repeat size. All paternal premutation allele contractions were transmitted as premutation alleles, but maternal premutation allele contractions were transmitted as premutation, intermediate, or normal alleles. The eight losses of AGG interruptions in the FMR1 repeat occurred exclusively in contractions of maternal premutation alleles. We propose a refined model of FMR1 repeat progression from normal to premutation size and suggest that most normal alleles without AGG interruptions are derived from contractions of maternal premutation alleles.
脆性X智力低下基因1(FMR1)重复序列的不稳定性在传递前突变等位基因(55 - 200次重复)时常见,它受重复序列大小、内部结构以及传递亲本的性别的影响。我们在14/3355个正常等位基因(约5至44次重复)、54/293个中间等位基因(45 - 54次重复)和1561/1880个前突变等位基因的不稳定传递中评估了这三个因素。虽然大多数不稳定传递导致扩增,但在所有大小类别中都观察到了向较小重复序列的收缩。对于正常等位基因,不稳定性在父系传递以及3'端具有长的不间断重复序列长度的等位基因中更常见。对于前突变等位基因,收缩在父系传递中也比母系传递中更频繁,并且父系收缩的频率随重复序列大小呈线性增加。所有父系前突变等位基因的收缩都以前突变等位基因的形式传递,但母系前突变等位基因的收缩则以前突变、中间或正常等位基因的形式传递。FMR1重复序列中AGG中断的八次缺失仅发生在母系前突变等位基因的收缩中。我们提出了一个从正常到前突变大小的FMR1重复序列进展的改进模型,并表明大多数没有AGG中断的正常等位基因源自母系前突变等位基因的收缩。