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由Pax2和Pax8介导的肾谱系特化

Nephric lineage specification by Pax2 and Pax8.

作者信息

Bouchard Maxime, Souabni Abdallah, Mandler Markus, Neubüser Annette, Busslinger Meinrad

机构信息

Research Institute of Molecular Pathology, Vienna Biocenter, A-1030 Vienna, Austria.

出版信息

Genes Dev. 2002 Nov 15;16(22):2958-70. doi: 10.1101/gad.240102.

Abstract

The mammalian kidney develops in three successive steps from the initial pronephros via the mesonephros to the adult metanephros. Although the nephric lineage is specified during pronephros induction, no single regulator, including the transcription factor Pax2 or Pax8, has yet been identified to control this initial phase of kidney development. In this paper, we demonstrate that mouse embryos lacking both Pax2 and Pax8 are unable to form the pronephros or any later nephric structures. In these double-mutant embryos, the intermediate mesoderm does not undergo the mesenchymal-epithelial transitions required for nephric duct formation, fails to initiate the kidney-specific expression of Lim1 and c-Ret, and is lost by apoptosis 1 d after failed pronephric induction. Conversely, retroviral misexpression of Pax2 was sufficient to induce ectopic nephric structures in the intermediate mesoderm and genital ridge of chick embryos. Together, these data identify Pax2 and Pax8 as critical regulators that specify the nephric lineage.

摘要

哺乳动物的肾脏发育经历三个连续阶段,从最初的前肾经中肾发育为成体后肾。尽管肾谱系在前肾诱导过程中就已确定,但尚未鉴定出包括转录因子Pax2或Pax8在内的单一调节因子来控制肾脏发育的这一初始阶段。在本文中,我们证明同时缺乏Pax2和Pax8的小鼠胚胎无法形成前肾或任何后续的肾结构。在这些双突变胚胎中,中间中胚层不会经历形成肾管所需的间充质-上皮转变,无法启动Lim1和c-Ret的肾脏特异性表达,并且在前肾诱导失败后1天因凋亡而消失。相反,Pax2的逆转录病毒错误表达足以在鸡胚的中间中胚层和生殖嵴中诱导异位肾结构。这些数据共同确定Pax2和Pax8是指定肾谱系的关键调节因子。

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