Suppr超能文献

水泡性口炎病毒合成核衣壳转录中血清型特异性的决定因素。

Determinants of serotype specificity in transcription of vesicular stomatitis virus synthetic nucleocapsids.

作者信息

Smallwood S, Richards-Sumners E, Moyer S A

机构信息

Department of Immunology and Medical Microbiology, College of Medicine, University of Florida, Gainesville 32610-0266.

出版信息

Virology. 1994 Feb 15;199(1):11-9. doi: 10.1006/viro.1994.1093.

Abstract

Transcription of the nucleocapsid template of vesicular stomatitis virus (VSV) is serotype specific, since the viral RNA polymerase of the VSV Indiana (Ind) serotype transcribes the Ind nucleocapsid but not the nucleocapsid of the VSV New Jersey (NJ) serotype and, similarly, the NJ RNA polymerase transcribes only the NJ nucleocapsid. We have prepared synthetic nucleocapsid templates from various combinations of purified leader gene RNA and N protein of these two VSV serotypes for analysis of serotype specificity in vitro. In agreement with previous observations, in vitro transcription of synthetic homologous nucleocapsids with the 3' terminal leader RNA gene of either the (+) or (-) strand sense and the N protein of the same serotype is also serotype specific. We show with chimeric nucleocapsids, where the RNA and N protein are of different serotypes, that both components of the template are important for specificity, although the specifics depend on the serotype from which the RNA polymerase is derived. The Ind RNA polymerase will transcribe only the homologous nucleocapsids where both the RNA and N protein are of the Ind serotype, and not the chimeric nucleocapsids. In contrast, the NJ RNA polymerase is active not only on the homologous synthetic nucleocapsid, but also gives significant levels of transcription as long as one of the nucleocapsid components (N protein or RNA) is of the NJ serotype. The divergent RNA sequence of the distal portion of the leader gene (nt22 to 50/51) seems to be a major determinant for specificity, since transcription of synthetic nucleocapsids containing just the conserved proximal 1-22 nucleotides is significantly less serotype-restricted. Restriction appears to occur at the level of elongation of the product rather than initiation of RNA synthesis, since synthesis of template-length RNA, but not reiterated small initiation products, is inhibited. In addition, the serotype of the P protein subunit of the RNA polymerase also contributes to the serotype specificity of transcription, since the NJ P protein can bind equally to NJ and Ind nucleocapsids, while Ind P protein binds preferentially to Ind nucleocapsids.

摘要

水疱性口炎病毒(VSV)核衣壳模板的转录具有血清型特异性,因为VSV印第安纳(Ind)血清型的病毒RNA聚合酶转录Ind核衣壳,而不转录VSV新泽西(NJ)血清型的核衣壳,同样,NJ RNA聚合酶仅转录NJ核衣壳。我们用这两种VSV血清型的纯化前导基因RNA和N蛋白的各种组合制备了合成核衣壳模板,用于体外分析血清型特异性。与先前的观察结果一致,用(+)或(-)链意义的3'末端前导RNA基因和相同血清型的N蛋白对合成同源核衣壳进行体外转录也具有血清型特异性。我们用RNA和N蛋白属于不同血清型的嵌合核衣壳表明,模板的两个组分对特异性都很重要,尽管具体情况取决于RNA聚合酶来源的血清型。Ind RNA聚合酶仅转录RNA和N蛋白均为Ind血清型的同源核衣壳,而不转录嵌合核衣壳。相比之下,NJ RNA聚合酶不仅对同源合成核衣壳有活性,而且只要核衣壳组分之一(N蛋白或RNA)是NJ血清型,就能产生显著水平的转录。前导基因远端部分(nt22至50/51)的不同RNA序列似乎是特异性的主要决定因素,因为仅包含保守近端1-22个核苷酸的合成核衣壳的转录受血清型限制的程度明显较低。限制似乎发生在产物延伸水平而非RNA合成起始水平,因为模板长度RNA的合成受到抑制,而重复性小起始产物的合成不受抑制。此外,RNA聚合酶P蛋白亚基的血清型也有助于转录的血清型特异性,因为NJ P蛋白能同等程度地结合NJ和Ind核衣壳,而Ind P蛋白优先结合Ind核衣壳。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验