Inoue M, Hosoda K, Imura K, Kamata S, Fukuzawa M, Nakao K, Okada A
Department of Pediatric Surgery, Osaka University Medical School, Japan.
J Pediatr Surg. 1998 Aug;33(8):1206-8. doi: 10.1016/s0022-3468(98)90151-8.
BACKGROUND/PURPOSE: Hirschsprung's disease (HD, HSCR) is one of the most common diseases in the field of pediatric surgery. It is well known that the aganglionic bowel is primarily a causative factor of dismotility of distal narrow segment. Recent studies have shown that mutations in endothelin-B receptor (EDNRB), endothelin-3, RET, glial cell line-derived neurotrophic factor (GDNF) genes are responsible for the occurrence of congenital aganglionosis. Here, the authors describe two new mutations of the EDNRB gene in Japanese patients with HD.
One patient had a heterozygous point mutation at the splice donor site of intron 3, leading to premature termination of translation of EDNRB mRNA. Another patient has a heterozygous missense mutation (N1041) in exon 1, but the same mutation was found in two of 50 normal individuals, so the mutation may be a noncausative polymorphism of the EDNRB gene.
These results provide further evidence that a spectrum of different mutations within the EDNRB gene are responsible for HD.
背景/目的:先天性巨结肠症(HD,HSCR)是小儿外科领域最常见的疾病之一。众所周知,无神经节肠段是导致远端狭窄段动力障碍的主要因素。最近的研究表明,内皮素B受体(EDNRB)、内皮素-3、RET、胶质细胞源性神经营养因子(GDNF)基因的突变与先天性无神经节症的发生有关。在此,作者描述了日本HD患者中EDNRB基因的两个新突变。
一名患者在内含子3的剪接供体位点存在杂合点突变,导致EDNRB mRNA翻译提前终止。另一名患者在外显子1中有一个杂合错义突变(N1041),但在50名正常个体中有两人也发现了相同的突变,因此该突变可能是EDNRB基因的非致病性多态性。
这些结果进一步证明,EDNRB基因内一系列不同的突变与HD有关。