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大鼠β-酪蛋白基因在转基因小鼠中的组织特异性表达。

Tissue-specific expression of the rat beta-casein gene in transgenic mice.

作者信息

Lee K F, DeMayo F J, Atiee S H, Rosen J M

机构信息

Department of Cell Biology, Baylor College of Medicine, Houston, TX 77030.

出版信息

Nucleic Acids Res. 1988 Feb 11;16(3):1027-41. doi: 10.1093/nar/16.3.1027.

Abstract

The rat beta-casein gene is a member of a small gene family, encoding the principal milk proteins. In order to understand the mechanisms by which its stage- and tissue-specific expression are regulated, initially, a 14 kb genomic clone containing the entire 7.5 kb rat beta-casein gene with 3.5 kb of 5' and 3.0 kb of 3' flanking DNA was microinjected into the germline of mice. Eight F0 transgenic mice were generated with copy numbers ranging from 1-10; five transmitted the transgene to their offspring in a Mendelian pattern. A specific RNase protection assay was developed to quantitate the level of expression of the rat beta-casein transgene as compared to the endogenous mouse beta-casein gene. Using this assay expression was demonstrated predominantly in the lactating mammary gland of transgenic mice at a level of 0.01-1% of the endogenous mouse beta-casein gene. The transgene employed the authentic transcription initiation site observed previously in the analogous rat beta-casein gene. In one line, a reduced level of expression of the transgene was also observed in the brain. The site of integration, therefore, plays an important role in influencing the level of expression of the transgene, but not its general pattern of tissue-specificity. The transgene appears to be developmentally-regulated in accordance with the endogenous mouse beta-casein gene. These lines of mice generated carrying the rat beta-casein transgene should provide useful models for studying the developmental and hormonal regulation of milk protein gene expression.

摘要

大鼠β-酪蛋白基因是一个小基因家族的成员,编码主要的乳蛋白。为了了解其阶段和组织特异性表达的调控机制,最初,将一个包含整个7.5 kb大鼠β-酪蛋白基因以及3.5 kb的5'侧翼DNA和3.0 kb的3'侧翼DNA的14 kb基因组克隆显微注射到小鼠的生殖系中。产生了8只F0转基因小鼠,拷贝数在1至10之间;其中5只以孟德尔方式将转基因传递给了它们的后代。开发了一种特异性核糖核酸酶保护试验,以定量大鼠β-酪蛋白转基因与内源性小鼠β-酪蛋白基因相比的表达水平。使用该试验表明,转基因主要在转基因小鼠的泌乳乳腺中表达,表达水平为内源性小鼠β-酪蛋白基因的0.01%-1%。转基因使用了先前在类似大鼠β-酪蛋白基因中观察到的真实转录起始位点。在一个品系中,还在大脑中观察到转基因表达水平降低。因此,整合位点在影响转基因表达水平方面起着重要作用,但不影响其组织特异性的总体模式。转基因似乎与内源性小鼠β-酪蛋白基因一样受到发育调控。这些携带大鼠β-酪蛋白转基因的小鼠品系应该为研究乳蛋白基因表达中的发育和激素调控提供有用的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c15e/334735/ba900a2a8afb/nar00145-0247-a.jpg

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