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Human and murine urokinase cDNAs linked to the murine alpha A-crystallin promoter exhibit lens and non-lens expression in transgenic mice

机译:与鼠αA-晶状蛋白启动子相连的人和鼠尿激酶cDNA在转基因小鼠中表现出晶状体和非晶状体表达

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摘要

cDNAs encoding either the human or the murine urokinase-type plasminogen activator (uPA) were fused downstream from the promoter-enhancer element of the murine gene encoding alpha A-crystallin, a protein found exclusively in the ocular lens. The DNAs were microinjected into fertilized mouse eggs as linear fragments free of bacterial sequences, and for each construct one line of transgenic mice was generated. In both lines transgenic uPA activity was detected in the ocular lens, in agreement with previous results reported on transgenic mice bearing genes fused to the same regulatory region. Unexpectedly however relatively high levels of this activity were found also in the retina, and furthermore, human uPA activity was found also in different parts of the brain and in the bone marrow, and to a lesser extent in the spleen, thymus and optic nerve. Transgenic uPA transcript was found in the lens, retina, brain and thymus of mice carrying the murine cDNA. Such a pattern of expression was different from that exhibited by the endogenous murine uPA gene and, excluding the lens, it appeared to be conferred by the cDNAs. The putative regulation by uPA cDNAs is suggested to be mediated through an internal enhancer-like element functioning in combination with the alpha A-crystallin promoter in a fashion independent of the specific nature of the promoter.
机译:将编码人或鼠尿激酶型纤溶酶原激活物(uPA)的cDNA融合到编码αA-crystallin的鼠基因的启动子增强子元件的下游,αA-crystallin是一种仅在眼晶状体中发现的蛋白质。将DNA以没有细菌序列的线性片段显微注射到受精的小鼠卵中,并且对于每种构建体,产生了一行转基因小鼠。在这两个系中,在眼晶状体中都检测到了转基因uPA活性,这与先前报道的携带融合到相同调控区域的基因的转基因小鼠的结果一致。然而,出乎意料的是,在视网膜中也发现了相对较高水平的这种活性,此外,还在大脑的不同部位和骨髓中以及在脾,胸腺和视神经中较小程度地发现了人uPA活性。在携带鼠cDNA的小鼠的晶状体,视网膜,大脑和胸腺中发现了转基因uPA转录物。这种表达方式不同于内源性鼠uPA基因所显示的表达方式,并且不包括晶状体,似乎是由cDNA赋予的。据推测,uPA cDNA的推测调控是通过内部增强子样元件介导的,该元件与αA-晶状蛋白启动子结合以独立于启动子特定性质的方式起作用。

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