Cheng Y S, Becker-Manley M F, Nguyen T D, DeGrado W F, Jonak G J
J Interferon Res. 1986 Aug;6(4):417-27. doi: 10.1089/jir.1986.6.417.
Upon the addition of interferon (IFN) to cultured human cells, the expression of genes encoding the 56K and the guanylate binding protein (GBP) is specifically induced. We have analyzed their expression at the protein and the mRNA levels and studied how their regulation differs in cells treated with different IFNs. In the type I IFN (alpha and beta)-treated cells, we detected the accumulation of the 56K protein primarily in the cytoplasm. The 56K protein was undetectable in untreated cells or in cells treated with type II IFN (IFN-gamma). In contrast, a greater amount of GBP was synthesized in cells treated with type II IFN than in cells treated with type I IFN. The differential induction of these two proteins correlates well with the relative amounts of their mRNAs in type I and type II IFN-treated cells. In addition, the IFN-induced synthesis of the 56K protein was found in certain cell lines in which the GBP synthesis was not detected. These results suggest that the regulation of these two genes requires dissimilar factors which are activated or induced to different extents by type I and type II IFNs.
在向培养的人类细胞中添加干扰素(IFN)后,编码56K和鸟苷酸结合蛋白(GBP)的基因表达会被特异性诱导。我们已经在蛋白质和mRNA水平上分析了它们的表达,并研究了在用不同干扰素处理的细胞中它们的调控方式有何不同。在I型干扰素(α和β)处理的细胞中,我们检测到56K蛋白主要在细胞质中积累。在未处理的细胞或用II型干扰素(IFN-γ)处理的细胞中未检测到56K蛋白。相反,与用I型干扰素处理的细胞相比,用II型干扰素处理的细胞中合成的GBP量更多。这两种蛋白的差异诱导与它们在I型和II型干扰素处理细胞中的mRNA相对量密切相关。此外,在某些未检测到GBP合成的细胞系中发现了干扰素诱导的56K蛋白合成。这些结果表明,这两个基因的调控需要不同的因子,这些因子在I型和II型干扰素作用下被不同程度地激活或诱导。