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通过中后脑组织者区域的表达谱分析鉴定Pax2调控的基因。

Identification of Pax2-regulated genes by expression profiling of the mid-hindbrain organizer region.

作者信息

Bouchard Maxime, Grote David, Craven Sarah E, Sun Qiong, Steinlein Peter, Busslinger Meinrad

机构信息

Research Institute of Molecular Pathology, Vienna Biocenter, Dr Bohr-Gasse 7, 1030 Vienna, Austria.

出版信息

Development. 2005 Jun;132(11):2633-43. doi: 10.1242/dev.01833. Epub 2005 May 4.

DOI:10.1242/dev.01833
PMID:15872005
Abstract

The paired domain transcription factor Pax2 is required for the formation of the isthmic organizer (IsO) at the midbrain-hindbrain boundary, where it initiates expression of the IsO signal Fgf8. To gain further insight into the role of Pax2 in mid-hindbrain patterning, we searched for novel Pax2-regulated genes by cDNA microarray analysis of FACS-sorted GFP+ mid-hindbrain cells from wild-type and Pax2-/- embryos carrying a Pax2(GFP) BAC transgene. Here, we report the identification of five genes that depend on Pax2 function for their expression in the mid-hindbrain boundary region. These genes code for the transcription factors En2 and Brn1 (Pou3f3), the intracellular signaling modifiers Sef and Tapp1, and the non-coding RNA Ncrms. The Brn1 gene was further identified as a direct target of Pax2, as two functional Pax2-binding sites in the promoter and in an upstream regulatory element of Brn1 were essential for lacZ transgene expression at the mid-hindbrain boundary. Moreover, ectopic expression of a dominant-negative Brn1 protein in chick embryos implicated Brn1 in Fgf8 gene regulation. Together, these data defined novel functions of Pax2 in the establishment of distinct transcriptional programs and in the control of intracellular signaling during mid-hindbrain development.

摘要

配对结构域转录因子Pax2是中脑-后脑边界处峡部组织者(IsO)形成所必需的,它在该区域启动IsO信号Fgf8的表达。为了更深入了解Pax2在中后脑模式形成中的作用,我们通过对携带Pax2(GFP)BAC转基因的野生型和Pax2基因敲除胚胎中经荧光激活细胞分选(FACS)得到的GFP+中后脑细胞进行cDNA微阵列分析,寻找新的Pax2调控基因。在此,我们报告鉴定出五个基因,它们在中后脑边界区域的表达依赖于Pax2的功能。这些基因编码转录因子En2和Brn1(Pou3f3)、细胞内信号修饰因子Sef和Tapp1以及非编码RNA Ncrms。Brn1基因被进一步鉴定为Pax2的直接靶标,因为Brn1启动子和上游调控元件中的两个功能性Pax2结合位点对于中后脑边界处lacZ转基因的表达至关重要。此外,在鸡胚中异位表达显性负性Brn1蛋白表明Brn1参与Fgf8基因调控。这些数据共同确定了Pax2在中后脑发育过程中建立不同转录程序和控制细胞内信号传导方面的新功能。

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