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小鼠矮胖突变破坏了Delta同源物Dll3以及早期体节边界的起始。

The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries.

作者信息

Kusumi K, Sun E S, Kerrebrock A W, Bronson R T, Chi D C, Bulotsky M S, Spencer J B, Birren B W, Frankel W N, Lander E S

机构信息

Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142, USA.

出版信息

Nat Genet. 1998 Jul;19(3):274-8. doi: 10.1038/961.

Abstract

Pudgy (pu) homozygous mice exhibit clear patterning defects at the earliest stages of somitogenesis, resulting in adult mice with severe vertebral and rib deformities. By positional cloning and complementation, we have determined that the pu phenotype is caused by a mutation in the delta-like 3 gene (Dll3), which is homologous to the Notch-ligand Delta in Drosophila. Histological and molecular marker analyses show that the pu mutation disrupts the proper formation of morphological borders in early somite formation and of rostral-caudal compartment boundaries within somites. Viability analysis also indicates an important role in early development. The results point to a key role for a Notch-signalling pathway in the initiation of patterning of vertebrate paraxial mesoderm.

摘要

矮胖(pu)纯合小鼠在体节发生的最早阶段就表现出明显的模式缺陷,导致成年小鼠出现严重的脊椎和肋骨畸形。通过定位克隆和互补分析,我们确定pu表型是由类Delta样3基因(Dll3)的突变引起的,该基因与果蝇中的Notch配体Delta同源。组织学和分子标记分析表明,pu突变破坏了早期体节形成中形态边界的正常形成以及体节内头尾节段边界的形成。生存力分析也表明其在早期发育中起重要作用。这些结果表明Notch信号通路在脊椎动物轴旁中胚层模式形成的起始中起关键作用。

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