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肝细胞核因子3β对于小鼠发育过程中节点和脊索的形成至关重要。

HNF-3 beta is essential for node and notochord formation in mouse development.

作者信息

Ang S L, Rossant J

机构信息

Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.

出版信息

Cell. 1994 Aug 26;78(4):561-74. doi: 10.1016/0092-8674(94)90522-3.

Abstract

HNF-3 beta, a member of the HNF-3/fork head family of transcription factors, is expressed in the node, notochord, floor plate, and gut in mouse embryos. A null mutation of this gene leads to embryonic lethality. The primary defect of HNF-3 beta -/- embryos is an absence of organized node and notochord formation, which leads to secondary defects in dorsal-ventral patterning of the neural tube. In contrast, patterning along the anterior-posterior axis was surprisingly little affected. Although HNF-3 beta is required for node and notochord formation, some organizer activity persists in the absence of these structures. HNF-3 beta is not required for the development of definitive endoderm cells, but foregut morphogenesis is severely affected in HNF-3 beta -/- embryos.

摘要

肝细胞核因子3β(HNF-3β)是转录因子HNF-3/叉头家族的成员之一,在小鼠胚胎的节点、脊索、底板和肠道中表达。该基因的无效突变导致胚胎致死。HNF-3β基因敲除胚胎的主要缺陷是缺乏有组织的节点和脊索形成,这导致神经管背腹模式的继发性缺陷。相比之下,前后轴的模式受到的影响出奇地小。虽然节点和脊索的形成需要HNF-3β,但在这些结构缺失的情况下,一些组织者活性仍然存在。确定的内胚层细胞的发育不需要HNF-3β,但HNF-3β基因敲除胚胎的前肠形态发生受到严重影响。

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