Constantoulakis P, Campbell M, Felber B K, Nasioulas G, Afonina E, Pavlakis G N
Human Retrovirus Section, National Cancer Institute-Frederick Cancer Research and Development Center, MD 21702.
Science. 1993 Feb 26;259(5099):1314-8. doi: 10.1126/science.7680491.
Interferon inhibits expression of human immunodeficiency virus type-1 (HIV-1) through unknown mechanisms. A gene inducible by interferon-alpha (IFN-alpha) and interferon-gamma (IFN-gamma) was isolated by screening of a human complementary DNA library for proteins binding to the Rev-responsive element (RRE) of HIV-1. The product of this gene, RBP9-27, was shown to bind RNA in vitro and to inhibit HIV-1 expression after transfection into human cells. RBP9-27 primarily inhibited Rev-dependent posttranscriptional steps of viral gene expression. Thus, RBP9-27 is a cellular factor that antagonizes Rev function. These results suggest an interferon-induced antiviral mechanism operating through the induction of RNA binding proteins such as RBP9-27. Elucidation of RBP9-27 function may lead to a better understanding of the mechanism of interferon action during HIV-1 infection.
干扰素通过未知机制抑制人类免疫缺陷病毒1型(HIV-1)的表达。通过筛选人类互补DNA文库中与HIV-1的Rev反应元件(RRE)结合的蛋白质,分离出一种可被α干扰素(IFN-α)和γ干扰素(IFN-γ)诱导的基因。该基因的产物RBP9-27在体外可与RNA结合,并在转染入人类细胞后抑制HIV-1的表达。RBP9-27主要抑制病毒基因表达中依赖Rev的转录后步骤。因此,RBP9-27是一种拮抗Rev功能的细胞因子。这些结果提示了一种干扰素诱导的抗病毒机制,该机制通过诱导如RBP9-27这样的RNA结合蛋白发挥作用。阐明RBP9-27的功能可能有助于更好地理解HIV-1感染期间干扰素的作用机制。