Schofield P N, Lindham S, Engström W
Department of Zoology, University of Oxford, United Kingdom.
Eur J Pediatr. 1989 Jan;148(4):320-4. doi: 10.1007/BF00444124.
The Beckwith-Wiedemann syndrome (BWS) is composed of multiple congenital malformations coupled with a high concurrent risk for the development of specific rare childhood tumours. The syndrome is characterised by a complex mode of inheritance, but recent evidence indicates that it is an autosomal dominant trait with variable penetrance. It has been previously suggested that major rearrangements of the short arm of chromosome 11 are involved in the aetiology of the disease. We undertook to search for rearrangements in 11p in four patients with BWS and their parents and siblings. By using cloned DNA fragments homologous to four genes located on 11p, namely catalase, parathyroid hormone, insulin-like growth factor II and the proto-oncogene c-Ha-Ras, we subjected DNA from the patients to a restriction fragment length polymorphism (RFLP) analysis after digestion with restriction enzymes. We found no evidence for any large scale deletions or amplifications in this chromosomal region. We therefore conclude that altered gene dosage is not, as has been suggested, a requirement for the development of BWS. This raises the question of whether some other molecular mechanism is responsible for the malformations observed.
贝克威思-维德曼综合征(BWS)由多种先天性畸形组成,同时患特定罕见儿童肿瘤的并发风险很高。该综合征的特征是遗传模式复杂,但最近的证据表明它是一种具有可变外显率的常染色体显性性状。以前曾有人提出,11号染色体短臂的重大重排与该疾病的病因有关。我们对4例BWS患者及其父母和兄弟姐妹进行了11p重排的研究。通过使用与位于11p上的4个基因(即过氧化氢酶、甲状旁腺激素、胰岛素样生长因子II和原癌基因c-Ha-Ras)同源的克隆DNA片段,我们在用限制性酶消化后,对患者的DNA进行了限制性片段长度多态性(RFLP)分析。我们没有发现该染色体区域存在任何大规模缺失或扩增的证据。因此我们得出结论,正如有人所提出的那样,基因剂量改变并非BWS发生的必要条件。这就提出了一个问题,即是否有其他分子机制导致了所观察到的畸形。