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在斑马鱼胚胎中,fgf8的转录受中脑-后脑边界处激活和抑制顺式元件的调控。

Transcription of fgf8 is regulated by activating and repressive cis-elements at the midbrain-hindbrain boundary in zebrafish embryos.

作者信息

Inoue Fumitaka, Parvin Mst Shahnaj, Yamasu Kyo

机构信息

Division of Life Science, Graduate School of Science and Engineering, Saitama University, Shimo-Okubo, Sakura-ku, Saitama City, Saitama 338-8570, Japan.

出版信息

Dev Biol. 2008 Apr 15;316(2):471-86. doi: 10.1016/j.ydbio.2008.01.013. Epub 2008 Jan 26.

Abstract

Fgf8 is expressed in the isthmic region of the developing brain, serving an organizing function in vertebrate embryos. We previously identified S4.2 downstream to the zebrafish fgf8 gene as a regulatory region that drives transcription in the anterior hindbrain. Here, we investigated the mechanism of fgf8 regulation by the S4.2 region during development. Reporter analyses in embryos revealed that S4.2 closely recapitulates fgf8 expression in the anteriormost hindbrain during somitogenesis. This region contains a sequence highly conserved in fgf8 of diverse vertebrates. Further analyses of S4.2 revealed a 342-bp core region composed of three subregions (#2, #3, and #4). Regions #3 and #4 drove expression broadly in the brain from the midbrain to r5 of the hindbrain, whereas a 28-bp sequence in #2 repressed ectopic expression in the midbrain and in r2 to r5. The enhancer function of S4.2 was absent in pax2a mutant embryos, while it was activated ectopically by pax2a misexpression in the hindbrain. We identified two sites in the core region that are bound by Pax2a in vitro and in vivo, the disruption of which abrogated the S4.2 activity. Thus, fgf8 expression in the anteriormost hindbrain involves activation and repression, with Pax2a as a pivotal regulator.

摘要

Fgf8在发育中的大脑峡部区域表达,在脊椎动物胚胎中发挥组织功能。我们之前确定斑马鱼fgf8基因下游的S4.2作为一个调控区域,驱动后脑前部的转录。在这里,我们研究了发育过程中S4.2区域对fgf8的调控机制。胚胎中的报告基因分析显示,在体节形成过程中,S4.2紧密重现了fgf8在最前端后脑的表达。该区域包含一个在多种脊椎动物的fgf8中高度保守的序列。对S4.2的进一步分析揭示了一个由三个子区域(#2、#3和#4)组成的342碱基对的核心区域。区域#3和#4在从后脑的中脑到r5的大脑中广泛驱动表达,而#2中的一个28碱基对序列抑制了中脑以及r2到r5中的异位表达。在pax2a突变胚胎中,S4.2的增强子功能缺失,而在后脑中通过pax2a的错误表达可异位激活该功能。我们在核心区域鉴定出两个在体外和体内都能被Pax2a结合的位点,破坏这些位点会消除S4.2的活性。因此,最前端后脑的fgf8表达涉及激活和抑制,其中Pax2a是关键调节因子。

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