Johnstone R W, Kerry J A, Trapani J A
The Austin Research Institute, Austin Hospital, Studley Road, Heidelberg 3084, Victoria, Australia.
J Biol Chem. 1998 Jul 3;273(27):17172-7. doi: 10.1074/jbc.273.27.17172.
IFI 16 is a member of a family of interferon-inducible proteins, including the human MNDA (myeloid nuclear differentiation antigen), the recently identified AIM-2 (absent in melanoma), and the homologous murine molecules, p202, p204, and D3. IFI 16 contains a domain at the amino terminus capable of binding double-stranded DNA and a bipartite nuclear localization signal. No molecular or biological function has been assigned to any of the human family members, although a role in transcription regulation has been proposed. In the present study, we show IFI 16 fused to the GAL4 DNA binding domain can function as a transcriptional repressor. IFI 16-mediated repression is not dependent on the position or distance of IFI 16 binding, relative to the site of transcription initiation, and it can significantly repress when only one GAL4 DNA element is present in the promoter. We mapped the transcriptional repression domains to the 200 amino acid repeat regions common to all human and mouse family members. We also demonstrate that wild type IFI 16 can repress transcription of a reporter gene containing the minimal promoter region of the human cytomegalovirus UL54 gene. Thus, IFI 16 is a transcriptional repressor, with a modular structure typical of many known transcription regulators.
IFI 16是干扰素诱导蛋白家族的成员之一,该家族还包括人类的MNDA(髓细胞核分化抗原)、最近发现的AIM-2(黑色素瘤缺失蛋白)以及同源的鼠类分子p202、p204和D3。IFI 16在氨基末端含有一个能够结合双链DNA的结构域和一个双分型核定位信号。尽管有人提出该人类家族成员在转录调控中发挥作用,但尚未赋予任何一个成员分子或生物学功能。在本研究中,我们发现与GAL4 DNA结合结构域融合的IFI 16可作为转录抑制因子发挥作用。IFI 16介导的抑制作用不依赖于IFI 16结合位点相对于转录起始位点的位置或距离,并且当启动子中仅存在一个GAL4 DNA元件时,它也能显著抑制。我们将转录抑制结构域定位到所有人类和小鼠家族成员共有的200个氨基酸重复区域。我们还证明野生型IFI 16能够抑制含有人类巨细胞病毒UL54基因最小启动子区域的报告基因的转录。因此,IFI 16是一种转录抑制因子,具有许多已知转录调节因子典型的模块化结构。