Der S D, Zhou A, Williams B R, Silverman R H
Department of Cancer Biology, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.
Proc Natl Acad Sci U S A. 1998 Dec 22;95(26):15623-8. doi: 10.1073/pnas.95.26.15623.
The pleiotropic activities of interferons (IFNs) are mediated primarily through the transcriptional regulation of many downstream effector genes. The mRNA profiles from IFN-alpha, -beta, or -gamma treatments of the human fibrosarcoma cell line, HT1080, were determined by using oligonucleotide arrays with probe sets corresponding to more than 6,800 human genes. Among these were transcripts for known IFN-stimulated genes (ISGs), the expression of which were consistent with previous studies in which the particular ISG was characterized as responsive to either Type I (alpha, beta) or Type II (gamma) IFNs, or both. Importantly, many novel IFN-stimulated genes were identified that were diverse in their known biological functions. For instance, several novel ISGs were identified that are implicated in apoptosis (including RAP46/Bag-1, phospholipid scramblase, and hypoxia inducible factor-1alpha). Furthermore, several IFN-repressed genes also were identified. These results demonstrate the usefulness of oligonucleotide arrays in monitoring mammalian gene expression on a broad and unprecedented scale. In particular, these findings provide insights into the basic mechanisms of IFN actions and ultimately may contribute to better therapeutic uses for IFNs.
干扰素(IFN)的多效性作用主要是通过对许多下游效应基因的转录调控来介导的。利用与6800多个人类基因对应的探针组的寡核苷酸阵列,测定了人纤维肉瘤细胞系HT1080经α-干扰素、β-干扰素或γ-干扰素处理后的mRNA谱。其中包括已知的干扰素刺激基因(ISG)的转录本,其表达与先前的研究一致,在先前的研究中,特定的ISG被鉴定为对I型(α、β)或II型(γ)干扰素或两者均有反应。重要的是,鉴定出了许多新型的干扰素刺激基因,它们的已知生物学功能各不相同。例如,鉴定出了几个与细胞凋亡有关的新型ISG(包括RAP46/Bag-1、磷脂翻转酶和缺氧诱导因子-1α)。此外,还鉴定出了几个干扰素抑制基因。这些结果证明了寡核苷酸阵列在以前所未有的广度监测哺乳动物基因表达方面的有用性。特别是,这些发现为干扰素作用的基本机制提供了见解,并最终可能有助于干扰素更好的治疗应用。