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2-氨基嘌呤选择性抑制β-干扰素、c-fos和c-myc基因表达的诱导。

2-Aminopurine selectively inhibits the induction of beta-interferon, c-fos, and c-myc gene expression.

作者信息

Zinn K, Keller A, Whittemore L A, Maniatis T

机构信息

Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, MA 02138.

出版信息

Science. 1988 Apr 8;240(4849):210-3. doi: 10.1126/science.3281258.

Abstract

The protein kinase inhibitor 2-aminopurine (2AP) blocks the induction of the human beta-interferon gene by virus or poly(I)-poly(C) at the level of transcription. This inhibition is specific, since 2AP does not inhibit induction of either the hsp70 heat-shock gene by high temperature or the metallothionein gene by cadmium or dexamethasone. However, 2AP does block the induction of the c-fos and c-myc proto-oncogenes by serum growth factors or virus, suggesting that a protein kinase may be involved in the regulation of these genes, as well as of the beta-interferon gene. However, different factors must be required for the induction of these three genes, since they are not coordinately regulated by the same inducers in most of the cell lines examined.

摘要

蛋白激酶抑制剂2-氨基嘌呤(2AP)在转录水平阻断病毒或聚肌苷酸-聚胞苷酸(poly(I)-poly(C))对人β-干扰素基因的诱导。这种抑制作用具有特异性,因为2AP不抑制高温对hsp70热休克基因的诱导,也不抑制镉或地塞米松对金属硫蛋白基因的诱导。然而,2AP确实能阻断血清生长因子或病毒对原癌基因c-fos和c-myc的诱导,这表明蛋白激酶可能参与这些基因以及β-干扰素基因的调控。然而,诱导这三个基因必定需要不同的因子,因为在大多数检测的细胞系中,它们并非由相同的诱导剂协同调控。

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