Kaku Yoshihiro, Chard Louisa S, Inoue Toru, Belsham Graham J
Department of Infectious Diseases, National Institute of Animal Health, Tsukuba, Ibaraki 305-0856, Japan.
J Virol. 2002 Nov;76(22):11721-8. doi: 10.1128/jvi.76.22.11721-11728.2002.
The teschoviruses constitute a recently defined picornavirus genus. Most of the genome sequence of the porcine teschovirus-1 (PTV) Talfan and several other strains is known. We now demonstrate that initiation of protein synthesis occurs at nucleotide (nt) 412 on the PTV Talfan RNA and that nt 1 to 405 contains an internal ribosome entry site (IRES) that functions efficiently in vitro and within mammalian cells. In comparison with other picornavirus IRES elements, the PTV IRES is relatively short and lacks a significant polypyrimidine tract near the 3' end. Expression of an enterovirus 2A protease, which induces cleavage of eIF4G within the translation initiation complex eIF4F, has little effect on the PTV IRES activity within BHK cells. The PTV IRES has a unique set of properties and represents a new class of picornavirus IRES element.
特斯可病毒属是最近定义的微小核糖核酸病毒属。猪特斯可病毒1型(PTV)塔尔凡株及其他几种毒株的大部分基因组序列已为人所知。我们现在证明,蛋白质合成起始于PTV塔尔凡RNA的第412位核苷酸(nt),并且第1至405位核苷酸包含一个内部核糖体进入位点(IRES),该位点在体外和哺乳动物细胞内均能高效发挥作用。与其他微小核糖核酸病毒IRES元件相比,PTV IRES相对较短,且在3'端附近缺乏明显的多嘧啶序列。肠道病毒2A蛋白酶的表达可诱导翻译起始复合物eIF4F内的eIF4G裂解,但对BHK细胞内的PTV IRES活性影响很小。PTV IRES具有一组独特的特性,代表了一类新型的微小核糖核酸病毒IRES元件。