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斑马鱼早期发育过程中foxe3的调控与功能

Regulation and function of foxe3 during early zebrafish development.

作者信息

Swindell Eric C, Zilinski Carolyn A, Hashimoto Ryuju, Shah Rina, Lane Mary Ellen, Jamrich Milan

机构信息

Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Genesis. 2008 Mar;46(3):177-83. doi: 10.1002/dvg.20380.

Abstract

In this article, we investigate the expression, regulation, and function of the zebrafish forkhead gene foxe3. In wild type embryos, foxe3 is first expressed in a crescent-shaped area at the anterior end of the prechordal plate, corresponding to the polster. At later stages, the hatching gland, the lens, and the anterior pituitary express this gene. Using morpholinos against the zinc finger Kruppel-like factor 4 (KLF4) we show that foxe3 is regulated differently in the polster and in the lens. In the absence of KLF4, expression of foxe3 in the polster is not activated, whereas in the lens placode the expression of KLF4 is not required for the transcription of foxe3. The expression of foxe3 is also regulated by the hedgehog and nodal signaling pathways. foxe3 expression is altered in the hedgehog pathway mutants iguana and you-too and the nodal pathway mutant cyclops. foxe3 function is necessary for the execution of lens-specific gene expression and lens morphogenesis, as the knockdown of foxe3 results in a loss of platelet-derived growth factor receptor alpha (pdgfralpha) expression and in the vacuolization of the lens.

摘要

在本文中,我们研究了斑马鱼叉头基因foxe3的表达、调控及功能。在野生型胚胎中,foxe3首先在前脊索板前端的新月形区域表达,该区域对应于基板。在后期阶段,孵化腺、晶状体和垂体前叶表达此基因。使用针对锌指Kruppel样因子4(KLF4)的吗啉代寡核苷酸,我们发现foxe3在基板和晶状体中的调控方式不同。在缺乏KLF4的情况下,foxe3在基板中的表达未被激活,而在晶状体原基中,foxe3的转录不需要KLF4的表达。foxe3的表达也受刺猬信号通路和节点信号通路调控。在刺猬信号通路突变体iguana和you-too以及节点信号通路突变体独眼巨人中,foxe3的表达发生改变。foxe3功能对于晶状体特异性基因表达的执行和晶状体形态发生是必需的,因为敲低foxe3会导致血小板衍生生长因子受体α(pdgfralpha)表达缺失以及晶状体空泡化。

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