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Pax2在中间中胚层中的表达受YY1调控。

Expression of Pax2 in the intermediate mesoderm is regulated by YY1.

作者信息

Patel Sanjeevkumar R, Dressler Gregory R

机构信息

Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI 48109, USA.

出版信息

Dev Biol. 2004 Mar 15;267(2):505-16. doi: 10.1016/j.ydbio.2003.11.002.

Abstract

The transcription factor Pax2 is essential for the development of the urogenital system. Pax2 expression can be detected by mouse embryonic day 8.5 (E8.5) in the region of intermediate mesoderm fated to become the nephric duct, pronephros, and mesonephros. Elements that direct Pax2 expression to nephrogenic precursor cells must be responding to positional information that controls nephrogenic fate. A 4.1-kb Pax2 promoter/enhancer fragment directs expression of a lacZ reporter to the nephrogenic region and the midbrain-hindbrain junction in transgenic mice. As kidney development proceeds, transgene expression is limited to the nephric duct and its derivatives, but not the metanephric mesenchyme. The early expression driven by the 4.1 promoter does not require the Pax2 protein, demonstrating that it receives positional information in the absence of a developing pro- or mesonephros. We have identified two DNAseI hypersensitive regions within this promoter, one at the start site of transcription initiation and a second approximately 2-kb upstream. Deletion of the more distal site significantly attenuates lacZ expression in the nephrogenic region but not in the midbrain-hindbrain region. DNA footprinting of this fragment revealed a highly conserved sequence between mouse and human Pax2 promoter sequences. Using fractionated nuclear extracts, we identified the transcription factor Yin Yang 1 (YY1) as the protein that binds to this conserved sequence. Deletion of the YY1 element significantly attenuated expression of a full-length 4.1 promoter. Moreover, inclusion of this YY1 binding element significantly enhanced expression of a minimal Pax2 promoter/enhancer transgene in E12 embryos. These data point to a novel role for YY1 in the establishment of high level tissue-specific expression within the intermediate mesoderm.

摘要

转录因子Pax2对于泌尿生殖系统的发育至关重要。在小鼠胚胎第8.5天(E8.5),可在注定会形成肾管、前肾和中肾的中间中胚层区域检测到Pax2的表达。将Pax2表达导向肾源性前体细胞的元件必定对控制肾源性命运的位置信息作出反应。一个4.1 kb的Pax2启动子/增强子片段可将lacZ报告基因的表达导向转基因小鼠的肾源性区域和中脑-后脑交界处。随着肾脏发育的进行,转基因表达局限于肾管及其衍生物,而不是后肾间充质。由4.1启动子驱动的早期表达不需要Pax2蛋白,这表明它在没有发育中的前肾或中肾的情况下接收位置信息。我们在该启动子内鉴定出两个DNA酶I超敏区域,一个在转录起始位点,另一个在大约上游2 kb处。删除更远端的位点会显著减弱肾源性区域中lacZ的表达,但不会影响中脑-后脑区域的表达。对该片段进行DNA足迹分析揭示了小鼠和人类Pax2启动子序列之间的高度保守序列。使用分级分离的核提取物,我们鉴定出转录因子阴阳1(YY1)是与该保守序列结合的蛋白质。删除YY1元件会显著减弱全长型4.1启动子的表达。此外,包含该YY1结合元件可显著增强E12胚胎中最小Pax2启动子/增强子转基因的表达。这些数据表明YY1在中间中胚层内高水平组织特异性表达的建立中具有新的作用。

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