Mechti N, Bisbal C, Leonetti J P, Salehzada T, Affabris E, Bayard B, Piechaczyk M, Blanchard J M, Jeanteur P, Lebleu B
UA CNRS 1191, Université de Montpellier II, France.
Biochimie. 1988 Jul;70(7):869-75. doi: 10.1016/0300-9084(88)90227-1.
This short review summarizes available evidence for (i) growth regulatory properties of exogenous as well as recently described autocrine IFNs, (ii) down-regulation of cellular oncogene expression with emphasis on c-myc and (iii) the possible involvement of the IFN-regulated 2-5A pathway at these levels. Initially described as a part of the IFN-induced antiviral mechanism, this double-stranded RNA-activated pathway leads to the preferential degradation of viral mRNAs in IFN-treated virus-infected cells probably through localized activation at the site of virus replication. Such mechanisms could be involved in the regulation of the stability of rapidly turning over mRNAs as for instance c-myc mRNA in IFN-treated cells. Whatever the elegance of the concept, however, experimental evidence is essentially circumstantial; tools developed in our group to strengthen the demonstration are briefly described.
(i) 外源性以及最近描述的自分泌干扰素的生长调节特性;(ii) 细胞癌基因表达的下调,重点是c-myc;(iii) 在这些水平上干扰素调节的2-5A途径可能的参与情况。该双链RNA激活途径最初被描述为干扰素诱导的抗病毒机制的一部分,在干扰素处理的病毒感染细胞中,它可能通过在病毒复制位点的局部激活导致病毒mRNA的优先降解。这种机制可能参与了如干扰素处理细胞中快速周转的mRNA(例如c-myc mRNA)稳定性的调节。然而,无论该概念多么精妙,实验证据基本上都是间接的;简要描述了我们小组开发的用于加强论证的工具。