首页> 外文OA文献 >trans activation of rat phosphoenolpyruvate carboxykinase (GTP) gene expression by micro-coinjection of rat liver mRNA in Xenopus laevis oocytes.
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trans activation of rat phosphoenolpyruvate carboxykinase (GTP) gene expression by micro-coinjection of rat liver mRNA in Xenopus laevis oocytes.

机译:通过在非洲爪蟾卵母细胞中微注射大鼠肝脏mRNA,反式激活大鼠磷酸烯醇丙酮酸羧化激酶(GTP)基因表达。

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摘要

To study the liver-specific trans activation of the rat phosphoenolpyruvate carboxykinase (PEPCK) gene, the PEPCK promoter was linked to a reporter gene and was microinjected into Xenopus laevis oocytes alone or in conjunction with rat liver poly(A)+ RNA. The rat liver mRNA markedly enhanced the expression of the PEPCK-chimeric construct. This effect appeared to be sequence specific, as it was dependent on the presence of the intact promoter. Moreover, the RNA effect was limited to mRNA preparations from PEPCK-expressing tissues only. Finally, microinjection of size-fractionated liver mRNA revealed that the trans-acting factor(s) is encoded by RNA of 1,600 to 2,000 nucleotides, providing a direct bioassay for the gene(s) involved in this tissue-specific trans-activation process.
机译:为了研究大鼠磷酸烯醇丙酮酸羧激酶(PEPCK)基因的肝脏特异性反式激活,将PEPCK启动子与一个报告基因相连,并将其单独或与大鼠肝脏poly(A)+ RNA一起显微注射到非洲爪蟾卵母细胞中。大鼠肝脏mRNA显着增强了PEPCK嵌合构建体的表达。该作用似乎是序列特异性的,因为它取决于完整启动子的存在。此外,RNA的作用仅限于表达PEPCK的组织的mRNA制备。最后,显微注射大小不等的肝脏mRNA显示,反式作用因子由1,600至2,000个核苷酸的RNA编码,为涉及该组织特异性反式激活过程的基因提供了直接的生物测定方法。

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