Analysis of the mechanism of translation initiation complex formation on feline calicivirus mRNA

猫杯状病毒mRNA翻译起始复合物形成机制分析

• 批准号: BB/D007755/1
• 负责人: Lisa Roberts
• 金额: $ 22.28万
• 依托单位: University of Surrey
• 依托单位国家: 英国
• 项目类别: Research Grant
• 财政年份: 2006
• 资助国家: 英国
• 起止时间: 2006 至 无数据
• 项目状态: 已结题
• 来源: https://gtr.ukri.org/projects?ref=BB%2FD007755%2F1
• 关键词: Analysis; mechanism; translation; initiation; complex

When viruses infect cells they need to utilise the host cell's protein synthesis machinery to synthesise new viral proteins. Viruses have therefore evolved a number of novel ways to ensure translation (or decoding) of their messenger RNAs (mRNAs) into protein in order to compete with cellular mRNAs. Members of the calicivirus family are responsible for important diseases of man and animals; noroviruses cause gastroenteritis or 'projectile vomiting' in humans and outbreaks are often seen in hospitals, cruise ships and in military camps, while feline calicivirus (FCV) causes cat 'flu. Currently, little is known about what happens when these viruses infect cells, and how new virus particles are made. We have shown that a viral protein attached to the end of the viral mRNAs (VPg) binds to a key cellular protein synthesis factor, eIF4E. This factor usually binds to a structure on cellular mRNAs (termed the 'cap') and helps recruit the protein synthesis machinery (including the ribosome). This suggests that caliciviruses utilise a novel mechanism to recruit ribosomes to their mRNAs, with VPg acting as a 'cap substitute'. We have also demonstrated that other cellular proteins bind to the FCV mRNA itself and may help to recruit ribosomes. We now aim to define further these interactions and the roles they play in virus protein synthesis and replication. This will aid in the development of novel antiviral therapies for this important group of viruses.

当病毒感染细胞时，它们需要利用宿主细胞的蛋白质合成机制来合成新的病毒蛋白质。因此，病毒已经进化出许多新的方法来确保它们的信使RNA（mRNA）翻译（或解码）成蛋白质，以便与细胞mRNA竞争。杯状病毒家族的成员负责人和动物的重要疾病;诺如病毒引起人类胃肠炎或“抛射性呕吐”，并且经常在医院，游轮和军营中爆发，而猫杯状病毒（FCV）引起猫流感。目前，人们对这些病毒感染细胞时会发生什么以及新病毒颗粒是如何产生的知之甚少。我们已经表明，连接到病毒mRNA（VPg）的末端的病毒蛋白质结合到一个关键的细胞蛋白质合成因子eIF 4 E。该因子通常与细胞mRNA上的结构（称为“帽”）结合，并帮助招募蛋白质合成机器（包括核糖体）。这表明杯状病毒利用一种新的机制将核糖体募集到它们的mRNA中，VPg充当“帽替代物”。我们还证明了其他细胞蛋白与FCV mRNA本身结合，可能有助于募集核糖体。我们现在的目标是进一步定义这些相互作用和它们在病毒蛋白质合成和复制中所起的作用。这将有助于开发针对这一重要病毒组的新型抗病毒疗法。

项目成果

Polypyrimidine tract binding protein functions as a negative regulator of feline calicivirus translation.

• DOI: 10.1371/journal.pone.0009562
• 发表时间: 2010-03-10
• 期刊: PloS one
• 影响因子: 3.7
• 作者: Karakasiliotis I;Vashist S;Bailey D;Abente EJ;Green KY;Roberts LO;Sosnovtsev SV;Goodfellow IG
• 通讯作者: Goodfellow IG