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Characterization of a hypoxia-response element in the Epo locus of the pufferfish, Takifugu rubripes

机译:河豚T(Takifugu rubripes)的Epo基因座中的缺氧响应元件的表征

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Animals respond to hypoxia by increasing synthesis of the glycoprotein hormone erythropoietin (Epo) which in turn stimulates the production of red blood cells. The gene encoding Epo has been recently cloned in teleost fishes such as the pufferfish Takifugu rubripes (fugu) and zebrafish (Danio rerio). It has been shown that the transcription levels of Epo in teleost fishes increase in response to anemia or hypoxia in a manner similar to its human ortholog. However, the cis-regulatory element(s) mediating the hypoxia response of Epo gene in fishes has not been identified. In the present study, using the human hepatoma cell line (Hep3B), we have identified and characterized a hypoxia response element (HRE) in the fugu Epo locus. The sequence of the fugu HRE (ACGTGCTG) is identical to that of the HRE in the human EPO locus. However, unlike the HRE in the mammalian Epo locus, which is located in the 3′ region of the gene, the fugu HRE is located in the 5′ flanking region and on the opposite strand of DNA. This HRE is conserved in other teleosts such as Tetraodon and zebrafish in a similar location. A 365-bp fragment containing the fugu HRE was able to drive GFP expression in the liver of transgenic zebrafish. However, we could not ascertain if the expression of transgene is induced by hypoxia in vivo due to the low and variable levels of GFP expression in transgenic zebrafish. Our investigations also revealed that the Epo locus has experienced extensive rearrangements during vertebrate evolution.
机译:动物通过增加糖蛋白激素促红细胞生成素(Epo)的合成来应对缺氧,进而刺激红血球的产生。最近,已经在硬骨鱼类中克隆了编码Epo的基因,例如河豚fish(Takifugu rubripes)和斑马鱼(Danio rerio)。已经显示硬骨鱼类中的Epo的转录水平以对​​人类贫血或缺氧的反应类似于其人类直系同源物的方式增加。然而,尚未确定介导鱼类中Epo基因低氧反应的顺式调控元件。在本研究中,我们使用人肝癌细胞系(Hep3B)在河豚Epo基因座中鉴定并鉴定了缺氧反应元件(HRE)。鼠类HRE(ACGTGCTG)的序列与人EPO基因座中HRE的序列相同。但是,与哺乳动物Epo基因座中位于基因3'区域的HRE不同,河豚HRE位于5'侧翼区域和DNA的相反链上。这种HRE在类似位置的其他硬骨鱼(如四齿龙和斑马鱼)中得到保存。含有fugu HRE的365 bp片段能够在转基因斑马鱼的肝脏中驱动GFP表达。但是,由于转基因斑马鱼中GFP的表达水平较低且可变,因此我们无法确定转基因的表达是否由体内低氧诱导。我们的研究还显示,Epo基因座在脊椎动物进化过程中经历了广泛的重排。

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