Bidaud C, Salomon R, Van Camp G, Pelet A, Attié T, Eng C, Bonduelle M, Amiel J, Nihoul-Fékété C, Willems P J, Munnich A, Lyonnet S
INSERM U-393, Département de Gńétique, and Clinique Chirurgicale Infantile, Hôpital des Enfants-Malades, Paris, France.
Eur J Hum Genet. 1997 Jul-Aug;5(4):247-51.
Hirschsprung disease (HSCR, aganglionic megacolon) is a frequent congenital malformation regarded as a multigenic neurocristopathy. Four susceptibility genes have recently been identified in HSCR, namely the RET proto-oncogene, the glial cell line-derived neurotrophic factor (GDNF), the endothelin B receptor (EDNRB) and the endothelin-3 genes (EDN3). Homozygosity for EDN3 mutations has been previously shown to cause the Shah-Waardenburg syndrome, a combination of HSCR with features of the Waardenburg syndrome. Here, we report on heterozygous EDN3 missense mutations in isolatec HSCR. The present data give further support to the role of the endothelin signaling pathway in the development of neural crest-derived enteric neurons. They also suggest the possibility that either recessive or weakly penetrant dominant alleles could occur at the EDN3 locus, depending on the nature of the mutation.
先天性巨结肠症(HSCR,无神经节性巨结肠)是一种常见的先天性畸形,被认为是一种多基因神经嵴病。最近在HSCR中鉴定出四个易感基因,即RET原癌基因、胶质细胞系源性神经营养因子(GDNF)、内皮素B受体(EDNRB)和内皮素-3基因(EDN3)。先前已证明EDN3突变的纯合子会导致沙阿-瓦登伯格综合征,这是一种HSCR与瓦登伯格综合征特征相结合的病症。在此,我们报告孤立性HSCR中的杂合性EDN3错义突变。目前的数据进一步支持了内皮素信号通路在神经嵴衍生的肠神经元发育中的作用。它们还表明,根据突变的性质,EDN3基因座可能出现隐性或弱显性等位基因。