Magee A C, Hughes A E
Regional Genetics Service, Belfast City Hospital Trust, Northern Ireland.
J Med Genet. 1998 Dec;35(12):1045-6. doi: 10.1136/jmg.35.12.1045.
Myotonic dystrophy (DM) is an autosomal dominant disease which, in the typical pedigree, shows a three generation anticipation cascade. This results in infertility and congenital myotonic dystrophy (CDM) with the disappearance of DM in that pedigree. The concept of segregation distortion, where there is preferential transmission of the larger allele at the DM locus, has been put forward to explain partially the maintenance of DM in the population. In a survey of DM in Northern Ireland, 59 pedigrees were ascertained. Sibships where the status of all the members had been identified were examined to determine the transmission of the DM expansion from affected parents to their offspring. Where the transmitting parent was male, 58.3% of the offspring were affected, and in the case of a female transmitting parent, 68.7% were affected. Studies on meiotic drive in DM have shown increased transmission of the larger allele at the DM locus in non-DM heterozygotes for CTGn. This study provides further evidence that the DM expansion tends to be transmitted preferentially.
强直性肌营养不良(DM)是一种常染色体显性疾病,在典型的家系中,呈现出三代遗传早现级联现象。这会导致不育以及先天性强直性肌营养不良(CDM),且该家系中的DM会消失。为部分解释DM在人群中的维持情况,人们提出了分离畸变的概念,即在DM位点存在较大等位基因的优先传递。在对北爱尔兰的DM调查中,确定了59个家系。对所有成员状态均已明确的同胞兄弟姐妹进行检查,以确定DM扩增从患病父母向其后代的传递情况。当传递亲本为男性时,58.3%的后代患病;而当传递亲本为女性时,68.7%的后代患病。对DM减数分裂驱动的研究表明,在CTGn的非DM杂合子中,DM位点较大等位基因的传递增加。本研究进一步证明了DM扩增倾向于优先传递。