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大鼠轻神经丝启动子驱动的报告基因在转基因小鼠中的组织特异性表达。

Tissue-specific expression of rat light neurofilament promoter-driven reporter gene in transgenic mice.

作者信息

Reeben M, Halmekytö M, Alhonen L, Sinervirta R, Saarma M, Jänne J

机构信息

Laboratory of Molecular Genetics, Institute of Chemical Physics and Biophysics, Tallinn, Estonia.

出版信息

Biochem Biophys Res Commun. 1993 Apr 30;192(2):465-70. doi: 10.1006/bbrc.1993.1438.

Abstract

We have produced nine transgenic mice lines carrying either 5 kbp or 407 bp of the 5' flanking sequence of the rat light neurofilament gene linked to the chloramphenicol acetyltransferase (CAT) structural gene. With the 5kb light neurofilament 5' flanking region governing the expression of CAT, reporter gene activity was detected not only in brain but also in the eye lens and skeletal muscle, yet not in other tissues. With the 407 bp construct, reporter gene activity was detected only in the brain, although expression was approximately one tenth of that found with the 5 kb 5' region. These results, together with earlier observations, indicate that the sequence -407 to -292 of the proximal promoter region for the light neurofilament gene or sequence +15 to +75 bp after the transcription initiation site is crucial for brain-specific expression of a fusion gene in transgenic mice.

摘要

我们已经培育出九条转基因小鼠品系,这些品系携带与氯霉素乙酰转移酶(CAT)结构基因相连的大鼠轻神经丝基因5'侧翼序列的5kb或407bp片段。在由5kb轻神经丝5'侧翼区域调控CAT表达的情况下,不仅在脑中检测到报告基因活性,在晶状体和骨骼肌中也检测到了,但在其他组织中未检测到。对于407bp构建体,仅在脑中检测到报告基因活性,尽管其表达量约为5kb 5'区域所观察到的十分之一。这些结果与早期观察结果一起表明,轻神经丝基因近端启动子区域的-407至-292序列或转录起始位点后+15至+75bp的序列对于转基因小鼠中融合基因的脑特异性表达至关重要。

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