Joutel A, Tournier-Lasserve E
INSERM U25, Faculté de Médecine, Necker-Enfants Malades, Paris, France.
Semin Cell Dev Biol. 1998 Dec;9(6):619-25. doi: 10.1006/scdb.1998.0261.
Several homologs of the Drosophila Notch receptor and its ligands, Delta/Serrate, have been cloned in man. Three human disorders including a neoplasia (a T-cell acute lymphoblastic leukemia/lymphoma), a late onset neurological disease (CADASIL) and a developmental disorder (the Alagille syndrome) are associated with mutations in, respectively, the Notch1, Notch3 and Jagged1 genes, pointing out the broad spectrum of Notch activity in humans. We report herein on what has been learned on the role of these human Notch genes and the mechanisms leading from mutations in those genes to the observed phenotypes.
果蝇Notch受体及其配体Delta/Serrate的几种同源物已在人类中克隆出来。三种人类疾病,包括一种肿瘤(T细胞急性淋巴细胞白血病/淋巴瘤)、一种迟发性神经疾病(大脑常染色体显性动脉病伴皮质下梗死和白质脑病,CADASIL)和一种发育障碍(阿拉吉列综合征),分别与Notch1、Notch3和Jagged1基因的突变相关,这表明Notch在人类中的活性范围很广。我们在此报告关于这些人类Notch基因的作用以及从这些基因的突变导致所观察到的表型的机制的相关研究成果。