Soh J, Donnelly R J, Kotenko S, Mariano T M, Cook J R, Wang N, Emanuel S, Schwartz B, Miki T, Pestka S
Department of Molecular Genetics and Microbiology, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, Piscataway 08854-5635.
Cell. 1994 Mar 11;76(5):793-802. doi: 10.1016/0092-8674(94)90354-9.
Human chromosomes 6 and 21 are both necessary to confer sensitivity to human interferon gamma (Hu-IFN-gamma), as measured by induction of class I human leukocyte antigen (HLA) and protection against encephalomyocarditis virus (EMCV) infection. Whereas human chromosome 6 encodes the Hu-IFN-gamma receptor, human chromosome 21 encodes accessory factors for generating biological activity through the Hu-IFN-gamma receptor. Probes from a genomic clone were used to identity cDNA clones expressing a species-specific accessory factor. These cDNA clones are able to substitute for human chromosome 21 to reconstitute the Hu-IFN-gamma receptor-mediated induction of class I HLA antigens. However, the factor encoded by the cDNA does not confer full antiviral protection against EMCV, confirming that an additional factor encoded on human chromosome 21 is required for reconstitution of antiviral activity against EMCV. We conclude that this accessory factor belongs to a family of such accessory factors responsible for different actions of IFN-gamma.
人类6号和21号染色体对于赋予对人γ干扰素(Hu-IFN-γ)的敏感性都是必需的,这是通过诱导I类人类白细胞抗原(HLA)以及抵抗脑心肌炎病毒(EMCV)感染来衡量的。虽然人类6号染色体编码Hu-IFN-γ受体,但人类21号染色体编码通过Hu-IFN-γ受体产生生物活性的辅助因子。来自基因组克隆的探针被用于鉴定表达物种特异性辅助因子的cDNA克隆。这些cDNA克隆能够替代人类21号染色体来重建Hu-IFN-γ受体介导的I类HLA抗原诱导。然而,cDNA编码的因子并不能赋予对EMCV的完全抗病毒保护,这证实了人类21号染色体上编码的另一种因子对于重建针对EMCV的抗病毒活性是必需的。我们得出结论,这种辅助因子属于负责IFN-γ不同作用的此类辅助因子家族。