Sharp T V, Schwemmle M, Jeffrey I, Laing K, Mellor H, Proud C G, Hilse K, Clemens M J
Department of Cellular and Molecular Sciences, St George's Hospital Medical School, London, UK.
Nucleic Acids Res. 1993 Sep 25;21(19):4483-90. doi: 10.1093/nar/21.19.4483.
The interferon-inducible protein kinase PKR interacts with a number of small viral RNA species, including adenovirus VAI RNA and the Epstein-Barr virus-encoded RNA EBER-1. These RNAs bind to PKR and protect protein synthesis from inhibition by double-stranded RNA in the reticulocyte lysate system. Using a peptide phosphorylation assay we show here that EBER-1, like VAI, directly inhibits the activation of purified PKR. A second Epstein-Barr virus RNA, EBER-2, also regulates PKR. EBER-1, EBER-2 and VAI RNA exhibit mutually competitive binding to the native or recombinant enzyme, as assessed by U.V. crosslinking experiments and filter binding assays. The affinities of all three RNAs for PKR in vitro are similar (Kd = ca. 0.3 nM). Since this protein kinase has been proposed to exert a tumour suppressor function in vivo, the ability of EBER-1 to inhibit its activation suggests a role for this small RNA in cell transformation by Epstein-Barr virus.
干扰素诱导蛋白激酶PKR可与多种小病毒RNA相互作用,包括腺病毒VAI RNA和爱泼斯坦-巴尔病毒编码的RNA EBER-1。这些RNA与PKR结合,在网织红细胞裂解液系统中保护蛋白质合成免受双链RNA的抑制。我们在此利用肽磷酸化试验表明,EBER-1与VAI一样,直接抑制纯化的PKR的激活。爱泼斯坦-巴尔病毒的另一种RNA,即EBER-2,也调节PKR。通过紫外线交联实验和滤膜结合试验评估,EBER-1、EBER-2和VAI RNA与天然或重组酶表现出相互竞争性结合。三种RNA在体外对PKR的亲和力相似(解离常数Kd约为0.3 nM)。由于该蛋白激酶在体内被认为具有肿瘤抑制功能,EBER-1抑制其激活的能力表明这种小RNA在爱泼斯坦-巴尔病毒介导的细胞转化中发挥作用。